elife03766.xml

<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Archiving and Interchange DTD v1.1d1 20130915//EN"  "JATS-archivearticle1.dtd"><article article-type="research-article" dtd-version="1.1d1" xmlns:xlink="http://www.w3.org/1999/xlink"><front><journal-meta><journal-id journal-id-type="nlm-ta">elife</journal-id><journal-id journal-id-type="hwp">eLife</journal-id><journal-id journal-id-type="publisher-id">eLife</journal-id><journal-title-group><journal-title>eLife</journal-title></journal-title-group><issn publication-format="electronic">2050-084X</issn><publisher><publisher-name>eLife Sciences Publications, Ltd</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">03766</article-id><article-id pub-id-type="doi">10.7554/eLife.03766</article-id><article-categories><subj-group subj-group-type="display-channel"><subject>Research article</subject></subj-group><subj-group subj-group-type="heading"><subject>Plant biology</subject></subj-group></article-categories><title-group><article-title>The kinase LYK5 is a major chitin receptor in <italic>Arabidopsis</italic> and forms a chitin-induced complex with related kinase CERK1</article-title></title-group><contrib-group><contrib contrib-type="author" equal-contrib="yes" id="author-15831"><name><surname>Cao</surname><given-names>Yangrong</given-names></name><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/><xref ref-type="fn" rid="equal-contrib">†</xref><xref ref-type="fn" rid="con1"/><xref ref-type="fn" rid="conf1"/></contrib><contrib contrib-type="author" equal-contrib="yes" id="author-15832"><name><surname>Liang</surname><given-names>Yan</given-names></name><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/><xref ref-type="fn" rid="equal-contrib">†</xref><xref ref-type="fn" rid="con2"/><xref ref-type="fn" rid="conf1"/></contrib><contrib contrib-type="author" id="author-15838"><name><surname>Tanaka</surname><given-names>Kiwamu</given-names></name><contrib-id contrib-id-type="orcid">http://orcid.org/0000-0001-5045-560X</contrib-id><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/><xref ref-type="fn" rid="pa1">‡</xref><xref ref-type="fn" rid="con3"/><xref ref-type="fn" rid="conf1"/></contrib><contrib contrib-type="author" id="author-15834"><name><surname>Nguyen</surname><given-names>Cuong T</given-names></name><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/><xref ref-type="fn" rid="con4"/><xref ref-type="fn" rid="conf1"/></contrib><contrib contrib-type="author" id="author-15835"><name><surname>Jedrzejczak</surname><given-names>Robert P</given-names></name><xref ref-type="aff" rid="aff3"/><xref ref-type="fn" rid="con5"/><xref ref-type="fn" rid="conf1"/></contrib><contrib contrib-type="author" id="author-15836"><name><surname>Joachimiak</surname><given-names>Andrzej</given-names></name><xref ref-type="aff" rid="aff3"/><xref ref-type="other" rid="par-3"/><xref ref-type="other" rid="par-4"/><xref ref-type="fn" rid="con6"/><xref ref-type="fn" rid="conf1"/></contrib><contrib contrib-type="author" corresp="yes" id="author-3525"><name><surname>Stacey</surname><given-names>Gary</given-names></name><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/><xref ref-type="corresp" rid="cor1">*</xref><xref ref-type="other" rid="par-1"/><xref ref-type="other" rid="par-2"/><xref ref-type="fn" rid="con7"/><xref ref-type="fn" rid="conf1"/></contrib><aff id="aff1"><institution content-type="dept">Division of Plant Sciences, National Center for Soybean Biotechnology</institution>, <institution>University of Missouri</institution>, <addr-line><named-content content-type="city">Columbia</named-content></addr-line>, <country>United States</country></aff><aff id="aff2"><institution content-type="dept">Department of Biochemistry</institution>, <institution>University of Missouri</institution>, <addr-line><named-content content-type="city">Columbia</named-content></addr-line>, <country>United States</country></aff><aff id="aff3"><institution content-type="dept">Midwest Center for Structural Genomics</institution>, <institution>Argonne National Laboratory</institution>, <addr-line><named-content content-type="city">Argonne</named-content></addr-line>, <country>United States</country></aff></contrib-group><contrib-group content-type="section"><contrib contrib-type="editor"><name><surname>Nürnberger</surname><given-names>Thorsten</given-names></name><role>Reviewing editor</role><aff><institution>Tübingen University</institution>, <country>Germany</country></aff></contrib></contrib-group><author-notes><corresp id="cor1"><label>*</label>For correspondence: <email>Staceyg@missouri.edu</email></corresp><fn fn-type="con" id="equal-contrib"><label>†</label><p>These authors contributed equally to this work</p></fn><fn fn-type="present-address" id="pa1"><label>‡</label><p>Department of Plant Pathology, Washington State University, Pullman, United States</p></fn></author-notes><pub-date date-type="pub" publication-format="electronic"><day>23</day><month>10</month><year>2014</year></pub-date><pub-date pub-type="collection"><year>2014</year></pub-date><volume>3</volume><elocation-id>e03766</elocation-id><history><date date-type="received"><day>27</day><month>06</month><year>2014</year></date><date date-type="accepted"><day>22</day><month>10</month><year>2014</year></date></history><permissions><license xlink:href="http://creativecommons.org/publicdomain/zero/1.0/"><license-p>This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the <ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/publicdomain/zero/1.0/">Creative Commons CC0 public domain dedication</ext-link>.</license-p></license></permissions><self-uri content-type="pdf" xlink:href="elife03766.pdf"/><abstract><object-id pub-id-type="doi">10.7554/eLife.03766.001</object-id><p>Chitin is a fungal microbe-associated molecular pattern recognized in <italic>Arabidopsis</italic> by a lysin motif receptor kinase (LYK), AtCERK1. Previous research suggested that AtCERK1 is the major chitin receptor and mediates chitin-induced signaling through homodimerization and phosphorylation. However, the reported chitin binding affinity of AtCERK1 is quite low, suggesting another receptor with high chitin binding affinity might be present. Here, we propose that AtLYK5 is the primary chitin receptor in <italic>Arabidopsis</italic>. Mutations in AtLYK5 resulted in a significant reduction in chitin response. However, AtLYK5 shares overlapping function with AtLYK4 and, therefore, <italic>Atlyk4/Atlyk5-2</italic> double mutants show a complete loss of chitin response. AtLYK5 interacts with AtCERK1 in a chitin-dependent manner. Chitin binding to AtLYK5 is indispensable for chitin-induced AtCERK1 phosphorylation. AtLYK5 binds chitin at a much higher affinity than AtCERK1. The data suggest that AtLYK5 is the primary receptor for chitin, forming a chitin inducible complex with AtCERK1 to induce plant immunity.</p><p><bold>DOI:</bold> <ext-link ext-link-type="doi" xlink:href="10.7554/eLife.03766.001">http://dx.doi.org/10.7554/eLife.03766.001</ext-link></p></abstract><abstract abstract-type="executive-summary"><object-id pub-id-type="doi">10.7554/eLife.03766.002</object-id><title>eLife digest</title><p>Invading fungi are responsible for many of the plant diseases that affect global crop production. Plants have to be able to identify these fungi, and activate the right defense strategies if they are to protect themselves. Chitin is a polymer that is found in the cell walls of all fungi, but not in plants, so if the plant detects chitin, it knows that a potentially harmful fungus may be nearby.</p><p>The detection of chitin, and the resulting activation of a plant's defenses, requires a receptor protein called CERK1. In rice, CERK1 needs to interact with another receptor protein called CEBiP, which binds to chitin. However, in <italic>Arabidopsis thaliana</italic>—which is widely studied in plant research—CERK1 can bind to chitin on its own, although this interaction is very weak, so it has been suggested that a second protein may be involved.</p><p>Cao et al. have now found that a receptor protein called LYK5, which is very similar to CERK1, is much better at attaching to chitin in <italic>A. thaliana</italic>. It can also bind to CERK1, but only when chitin is present, and is required for activation of basic plant defenses. The experiments suggest that LYK5 detects chitin on behalf of CERK1, in a similar way to how CEBiP works in rice.</p><p>The next step in this research is to work out how CERK1 and LYK5 are able to activate plant defenses.</p><p><bold>DOI:</bold> <ext-link ext-link-type="doi" xlink:href="10.7554/eLife.03766.002">http://dx.doi.org/10.7554/eLife.03766.002</ext-link></p></abstract><kwd-group kwd-group-type="author-keywords"><title>Author keywords</title><kwd><italic>Arabidoposis</italic></kwd><kwd>plant innate immunity</kwd><kwd>chitin receptor</kwd><kwd>CERK1</kwd><kwd>LYK5</kwd></kwd-group><kwd-group kwd-group-type="research-organism"><title>Research organism</title><kwd><italic>Arabidopsis</italic></kwd></kwd-group><funding-group><award-group id="par-1"><funding-source><institution-wrap><institution-id institution-id-type="FundRef">http://dx.doi.org/10.13039/501100003627</institution-id><institution>Rural Development Administration</institution></institution-wrap></funding-source><award-id>Next-Generation BioGreen 21 Program Systems and Synthetic Agrobiotech CenterPJ009068</award-id><principal-award-recipient><name><surname>Stacey</surname><given-names>Gary</given-names></name></principal-award-recipient></award-group><award-group id="par-2"><funding-source><institution-wrap><institution-id institution-id-type="FundRef">http://dx.doi.org/10.13039/100006151</institution-id><institution>Basic Energy Sciences</institution></institution-wrap></funding-source><award-id>DE-FG02-08ER15309</award-id><principal-award-recipient><name><surname>Stacey</surname><given-names>Gary</given-names></name></principal-award-recipient></award-group><award-group id="par-3"><funding-source><institution-wrap><institution-id institution-id-type="FundRef">http://dx.doi.org/10.13039/100006206</institution-id><institution>Biological and Environmental Research</institution></institution-wrap></funding-source><award-id>DE-AC02-06CH11357</award-id><principal-award-recipient><name><surname>Joachimiak</surname><given-names>Andrzej</given-names></name></principal-award-recipient></award-group><award-group id="par-4"><funding-source><institution-wrap><institution-id institution-id-type="FundRef">http://dx.doi.org/10.13039/100000002</institution-id><institution>National Institutes of Health</institution></institution-wrap></funding-source><award-id>GM094585</award-id><principal-award-recipient><name><surname>Joachimiak</surname><given-names>Andrzej</given-names></name></principal-award-recipient></award-group><funding-statement>The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.</funding-statement></funding-group><custom-meta-group><custom-meta><meta-name>elife-xml-version</meta-name><meta-value>2</meta-value></custom-meta><custom-meta specific-use="meta-only"><meta-name>Author impact statement</meta-name><meta-value>The chitin-triggered immune response is mediated by a LYK5 and CERK1 receptor complex in Arabidopsis.</meta-value></custom-meta></custom-meta-group></article-meta></front><body><sec id="s1" sec-type="intro"><title>Introduction</title><p>As sessile organisms, plants have developed effective immune systems to defend against invading pathogens. Pathogen perception in plants can be divided into two different layers (<xref ref-type="bibr" rid="bib21">Jones and Dangl, 2006</xref>). The initial response, mediated by perception of microbe-associated molecular patterns (MAMPs), is termed MAMP-triggered immunity (MTI) (<xref ref-type="bibr" rid="bib5">Boller and Felix, 2009</xref>; <xref ref-type="bibr" rid="bib34">Macho and Zipfel, 2014</xref>). MTI is characterized by a wide range of physiological responses, including production of reactive oxygen species (ROS), mitogen activated protein kinase (MAPK) phosphorylation, calcium influx, ion channel activation, callose deposition, growth inhibition, and expression of defense-related genes (<xref ref-type="bibr" rid="bib34">Macho and Zipfel, 2014</xref>). However, adapted pathogens can inhibit MTI through the secretion of specific effector proteins or small RNAs into the cell (<xref ref-type="bibr" rid="bib62">Weiberg et al., 2013</xref>, <xref ref-type="bibr" rid="bib61">2014</xref>). In response, plants have evolved polymorphic nucleotide-binding site leucine-rich repeat (NBS-LRR) proteins that either directly or indirectly recognize these effectors; thereby, restoring plant immunity. This form of immunity is termed effector-triggered immunity (ETI) (<xref ref-type="bibr" rid="bib3">Bent and Mackey, 2007</xref>; <xref ref-type="bibr" rid="bib5">Boller and Felix, 2009</xref>). Compared to MTI, ETI is much stronger and often associated with a hypersensitive response (HR), which involves programmed cell death (<xref ref-type="bibr" rid="bib21">Jones and Dangl, 2006</xref>).</p><p>Plants use cell-surface localized pattern-recognition receptors (PRRs) to detect MAMPs activating MTI (<xref ref-type="bibr" rid="bib5">Boller and Felix, 2009</xref>; <xref ref-type="bibr" rid="bib34">Macho and Zipfel, 2014</xref>). In plants, several PRRs have been well characterized, including FLAGELLIN-SENSING 2 (FLS2) and elongation factor-TU (EF-Tu) RECEPTOR (EFR), which detect bacterial flagellin and EF-Tu, respectively (<xref ref-type="bibr" rid="bib14">Gomez-Gomez and Boller, 2000</xref>, <xref ref-type="bibr" rid="bib13">2002</xref>; <xref ref-type="bibr" rid="bib67">Zipfel et al., 2006</xref>). These two receptors belong to the leucine rich repeat receptor like protein kinase (LRR-RLK) family (<xref ref-type="bibr" rid="bib51">Shiu and Bleecker, 2001</xref>). Activation of these receptors by ligand binding induces the association with BRASSINOSTEROID INSENSITIVE 1 (BRI1)- Associated receptor Kinase 1 (BAK1) and phosphorylation of Botrytis-Induced Kinase (BIK1) (<xref ref-type="bibr" rid="bib9">Chinchilla et al., 2007</xref>; <xref ref-type="bibr" rid="bib18">Heese et al., 2007</xref>; <xref ref-type="bibr" rid="bib33">Lu et al., 2010</xref>; <xref ref-type="bibr" rid="bib46">Roux et al., 2011</xref>; <xref ref-type="bibr" rid="bib66">Zhang et al., 2010</xref>). Phosphorylated BIK1 dissociates from the receptor and subsequently phosphorylates the respiratory burst oxidase homolog D (RBOHD) protein, which controls ROS production in a calcium-independent manner (<xref ref-type="bibr" rid="bib22">Kadota et al., 2014</xref>; <xref ref-type="bibr" rid="bib27">Li et al., 2014</xref>). Other MAMPs, such as the oligosaccharides bacterial peptidoglycan (PGN) and fungal chitin [degree of polymerization (dp) ≥ 6], are detected by lysin-motif (LysM) containing proteins. The chitin receptor was first reported in rice with the identification of the chitin-elicitor binding protein (CEBiP) (<xref ref-type="bibr" rid="bib23">Kaku et al., 2006</xref>), which contains an extracellular LysM motif and a transmembrane domain, but lacks an intracellular kinase domain. Data indicate that CEBiP forms a complex with the rice chitin-elicitor receptor kinase 1 (OsCERK1) to mediate MTI in response to chitin (<xref ref-type="bibr" rid="bib17">Hayafune et al., 2014</xref>; <xref ref-type="bibr" rid="bib49">Shimizu et al., 2010</xref>). OsCERK1 has an active, intracellular kinase domain. The data suggest that OsCERK1 does not bind chitin but its intracellular kinase domain is activated by chitin binding to OsCEBiP (<xref ref-type="bibr" rid="bib17">Hayafune et al., 2014</xref>). In <italic>Arabidopsis thaliana</italic>, AtCERK1 was shown to be a key chitin receptor involved in chitin perception (<xref ref-type="bibr" rid="bib38">Miya et al., 2007</xref>; <xref ref-type="bibr" rid="bib59">Wan et al., 2008</xref>). For example, <italic>Atcerk1</italic> mutant plants completely lose the ability to respond to chitin elicitation. There are three homologs of CEBiP in <italic>Arabidopsis</italic>, but a triple knock-out mutant, <italic>Atlym1/Atlym2/Atlym3</italic> lacking these three proteins was fully competent to respond to chitin treatment (<xref ref-type="bibr" rid="bib58">Wan et al., 2012</xref>). However, two CEBiP like proteins appear to function in conjunction with CERK1 to mediate recognition of bacterial PGN (OsLYP4 and OsLYP6 in rice, AtLYM1 and AtLYM3 in <italic>Arabidopsis</italic>) (<xref ref-type="bibr" rid="bib31">Liu et al., 2012a</xref>; <xref ref-type="bibr" rid="bib63">Willmann et al., 2011</xref>). Another CEBiP-like protein, AtLYM2, was demonstrated to act independently of AtCERK1 to mediate chitin-induced suppression of intracellular flux through plasmodesmata (<xref ref-type="bibr" rid="bib12">Faulkner et al., 2013</xref>).</p><p>In <italic>Arabidopsis</italic>, there are five members of the lysin-motif receptor like kinase family (LYKs), that is, AtCERK1/LysM RLK1/AtLYK1, and AtLYK2-5 (<xref ref-type="bibr" rid="bib58">Wan et al., 2012</xref>). AtCERK1 was reported as the primary chitin receptor based on the mutant phenotype (<xref ref-type="bibr" rid="bib38">Miya et al., 2007</xref>; <xref ref-type="bibr" rid="bib59">Wan et al., 2008</xref>) but also the fact that the protein can be precipitated by binding to chitin beads (<xref ref-type="bibr" rid="bib19">Iizasa et al., 2010</xref>; <xref ref-type="bibr" rid="bib44">Petutschnig et al., 2010</xref>). The X-ray crystal structure of the ectodomain of AtCERK1 was solved by <xref ref-type="bibr" rid="bib32">Liu et al. (2012b)</xref>. The structure predicted interaction of chitin oligomers with the second LysM motif in the extracellular domain. These authors suggested a model by which long chain chitin oligomers (dp ≥ 6) bound to the LysM domains on two monomers, resulting in homodimerization of AtCERK1. This dimerization was shown to activate the intracellular kinase domain (<xref ref-type="bibr" rid="bib32">Liu et al., 2012b</xref>; <xref ref-type="bibr" rid="bib44">Petutschnig et al., 2010</xref>). However, there remains the possibility that, similar to the situation in rice, the active chitin receptor is composed of more than one protein. For example, mutations in <italic>AtLYK4</italic> were shown to significantly reduce the plant response to chitin (<xref ref-type="bibr" rid="bib58">Wan et al., 2012</xref>), although the phenotype was not as pronounced as that of <italic>Atcerk1</italic> mutant plants. While the X-ray crystal structure of the ectodomain of AtCERK1 provided evidence that it is indeed a chitin binding protein, a puzzling aspect of this work is the low binding affinity (chitooctaose, K<sub>d</sub> = 45 µM) reported, based on calorimetry (<xref ref-type="bibr" rid="bib32">Liu et al., 2012b</xref>). Another puzzling aspect is that mutations in AtCERK1, predicted to block chitin binding (AtCERK1<sup>A138H</sup>), did not block chitin-induced AtCERK1<sup>A138H</sup> phosphorylation (<xref ref-type="bibr" rid="bib32">Liu et al., 2012b</xref>). These data led us to consider the possibility that a second protein may be involved that mediates high affinity chitin binding and works with AtCERK1 to activate MTI.</p><p>In this study, we show that mutations in AtLYK5 result in a significant reduction in the plant chitin response. AtLYK5 is required for chitin-induced AtCERK1 homodimerization and phosphorylation. AtLYK5 binds to chitin with a much higher affinity than AtCERK1. The data suggest that AtLYK5 is the primary receptor for chitin, forming a chitin-inducible complex with AtCER<sc>K1</sc> to induce plant innate immunity.</p></sec><sec id="s2" sec-type="results"><title>Results</title><sec id="s2-1"><title>AtLYK5 is essential for the chitin response in <italic>Arabidopsis</italic></title><p><italic>Arabidopsis</italic> has five LysM receptor kinases (LYKs) (<xref ref-type="fig" rid="fig1s1">Figure 1—figure supplement 1</xref>). Therefore, plants mutated in each of these genes were tested for their ability to induce reactive oxygen species (ROS) in response to chitin elicitation. As expected from previous publications, mutations in <italic>AtCERK1</italic> showed strongly reduced ROS production (<xref ref-type="bibr" rid="bib38">Miya et al., 2007</xref>; <xref ref-type="bibr" rid="bib59">Wan et al., 2008</xref>), while mutations in <italic>AtLYK4</italic> also showed a slight reduction in ROS production upon chitin elicitation (<xref ref-type="bibr" rid="bib58">Wan et al., 2012</xref>). In previous publications, which involved screening <italic>Atlyk1-5</italic> mutants, we reported that a transposon insertion in <italic>AtLYK5</italic> did not affect chitin-induced MTI (<xref ref-type="bibr" rid="bib59">Wan et al, 2008</xref>, <xref ref-type="bibr" rid="bib58">2012</xref>). This conclusion was based on measuring <italic>AtWRKY53</italic> expression upon chitin addition<italic>.</italic> At the time of these studies, the only <italic>Atlyk5</italic> mutant available was in the Lansberg (Ler) background (<italic>Atlyk5-1</italic>). As part of a new round of screening, we again examined the chitin response of <italic>Atlyk5-1</italic> mutant plants. qRT-PCR analysis showed that chitin treatment induced similar expression of <italic>AtWRKY53</italic> in both Ler wild-type and <italic>Atlyk5-1</italic> mutant plants (<xref ref-type="fig" rid="fig1s2">Figure 1—figure supplement 2</xref>); data consistent with the previously published results (<xref ref-type="bibr" rid="bib59">Wan, et al, 2008</xref>, <xref ref-type="bibr" rid="bib58">2012</xref>). However, in contrast to these results, the expression of <italic>AtWRKY33</italic> 15 min after chitin treatment was significantly reduced in <italic>Atlyk5-1</italic> mutant plants relative to Ler wild-type plants (<xref ref-type="fig" rid="fig1s2">Figure 1—figure supplement 2</xref>). Chitin-triggered MAP kinase (MPK) phosphorylation was also significantly reduced in <italic>Atlyk5-1</italic> mutant plants compared with Ler wild-type plants (<xref ref-type="fig" rid="fig1s2">Figure 1—figure supplement 2</xref>). The phosphorylated AtCERK1 triggered by chitin elicitation can be detected as a band shift based on immunoblots using anti-AtCERK1 antibody (<xref ref-type="fig" rid="fig1s2">Figure 1—figure supplement 2</xref>) (<xref ref-type="bibr" rid="bib32">Liu et al., 2012b</xref>; <xref ref-type="bibr" rid="bib44">Petutschnig et al., 2010</xref>). Chitin-triggered AtCERK1 phosphorylation was detected in Ler wild-type plants but was reduced in <italic>Atlyk5-1</italic> mutant plants (<xref ref-type="fig" rid="fig1s2">Figure 1—figure supplement 2</xref>). In general, based on chitin-triggered ROS production, Ler wild-type plants showed a lower response to chitin than Col-0 plants, while <italic>Atlyk5-1</italic> mutant plants showed similar ROS production to the wild-type when treated with chitin (<xref ref-type="fig" rid="fig1s2">Figure 1—figure supplement 2</xref>). Taken together, these experiments suggested that our original conclusion concerning AtLYK5 may not be correct; that is, this protein may be involved in chitin response. What is clear is that the <italic>Atlyk5-1</italic> mutant, with a transposon insertion in the 3′ region of the gene, does not exhibit a strong phenotype under all conditions. The analysis of the chitin response in the Ler ecotype is further complicated by the generally weak response to chitin elicitation.</p><p>Given these concerns, we identified and characterized a Col-0 <italic>Atlyk5</italic> mutant (<italic>Atlyk5-2</italic>) from the SALK population (<xref ref-type="fig" rid="fig1s3">Figure 1—figure supplement 3</xref>). This line has a T-DNA in the extracellular domain of AtLYK5 (<xref ref-type="fig" rid="fig1s3">Figure 1—figure supplement 3</xref>). It should be noted that in our original publications (<xref ref-type="bibr" rid="bib59">Wan et al., 2008</xref>, <xref ref-type="bibr" rid="bib58">2012</xref>), all of the <italic>Atlyk</italic> mutants, with the exception of <italic>Atlyk5-1</italic>, were derived from the Col-0 ecotype. As shown in <xref ref-type="fig" rid="fig1">Figure 1A</xref>, chitin-induced ROS production was significantly lower in the <italic>Atlyk5-2</italic> mutant plants compared to Col-O wild-type plants (<xref ref-type="fig" rid="fig1">Figure 1A</xref>). Calcium influx is activated by exposure of wild-type plants to chitin. Similar treatment of <italic>Atlyk5-2</italic> mutant plants showed a 90% reduction and a significant delay in the calcium response, while <italic>Atcerk1</italic> mutant plants showed essentially no calcium response to chitin (<xref ref-type="fig" rid="fig1">Figure 1B</xref>). Flagellin-triggered calcium influx in both <italic>Atcerk1</italic> and <italic>Atlyk5-2</italic> mutant plants were similar to Col-0 wild-type plants (<xref ref-type="fig" rid="fig1s4">Figure 1—figure supplement 4</xref>), indicating that these defects were specific to chitin and not to a general effect on MTI. MPK3 and MPK6 are specifically phosphorylated upon chitin elicitation in Col-0 wild-type but not in <italic>Atcerk1</italic> mutant plants. Significant reduction in MPK phosphorylation was detected in <italic>Atlyk5-2</italic> mutant plants after chitin treatment (<xref ref-type="fig" rid="fig1">Figure 1C</xref>). Consistent with these findings, the <italic>Atlyk5-2</italic> mutant plants showed an intermediate response with regard to chitin-induced <italic>AtWRKY29, AtWRKY30, AtWRKY33,</italic> and <italic>AtWRKY53</italic> expression compared to the Col-0 wild-type and the <italic>Atcerk1</italic> mutant plants (<xref ref-type="fig" rid="fig1">Figure 1D,E</xref>, <xref ref-type="fig" rid="fig1s4">Figure 1—figure supplement 4</xref>). Both <italic>Atcerk1</italic> and <italic>Atlyk5-2</italic> mutant plants showed increased susceptibility to the fungal pathogen <italic>Alternaria brassicicola</italic> compared with Col-0 wild-type plants. Pretreatment with chitooctaose enhanced resistance to <italic>A. brassicicola</italic> in wild-type plants but not in <italic>Atcerk1</italic> or <italic>Atlyk5-2</italic> mutant plants (<xref ref-type="fig" rid="fig1">Figure 1F</xref>). Untreated <italic>Atcerk1</italic> and <italic>Atlyk5-2</italic> mutant plants showed wild-type levels of resistance to the bacterial pathogen <italic>Pseudomonas syringae</italic> pv. tomato DC3000. However, only the wild-type showed increased bacterial resistance when plants were pretreated with chitooctaose to induce MTI (<xref ref-type="fig" rid="fig1">Figure 1G</xref>). In order to confirm that the loss of chitin response was due to the <italic>AtLYK5</italic> mutation, transgenic plants expressing the full-length <italic>AtLYK5</italic> gene were generated under control of its native promoter in the <italic>Atlyk5-2</italic> mutant genetic background (<xref ref-type="fig" rid="fig2s1">Figure 2—figure supplement 1</xref>). Expression of AtLYK5 in <italic>Atlyk5-2</italic> mutant plants complemented all of the chitin-induced responses, including ROS production and MAPK phosphorylation (<xref ref-type="fig" rid="fig2s1">Figure 2—figure supplement 1</xref>). These data indicate that AtLYK5 is essential for a strong response to chitin elicitation. The response of all five <italic>Atlyk</italic> mutant plants was tested based on chitin-induced ROS prodction (<xref ref-type="fig" rid="fig1s5">Figure 1—figure supplement 5</xref>), confirming that AtCERK1, AtLYK4 and AtLYK5, but not AtLYK2 or AtLYK3 are involved in chitin signaling.<fig-group><fig id="fig1" position="float"><object-id pub-id-type="doi">10.7554/eLife.03766.003</object-id><label>Figure 1.</label><caption><title><italic>Atlyk5</italic> mutant plants are defective in chitin-triggered immune responses.</title><p>(<bold>A</bold>) ROS production was measured from Col-0 wild-type and <italic>Atlyk5-2</italic> mutant plants for 30 min after treatment with different chitin oligomers. 5mer: chitopentaose, 6mer: chitohexaose, 7mer: chitoheptaose, and 8mer: chitooctaose. Data are mean ± SE (n = 8). Asterisks indicate significant difference relative to H<sub>2</sub>O treated Col-0 wild-type plants. (p &lt; 0.01, Student's <italic>t</italic> test). (<bold>B</bold>) Calcium influx in the wild-type, <italic>Atcerk1</italic> and <italic>Atlyk5-2</italic> mutant plants expressing aequorin was recorded for 30 min after chitooctaose treatment. (<bold>C</bold>) MAP kinase phosphorylation after chitooctaose treatment was detected by immunoblot using anti-P44/P42 antibody. (<bold>D</bold>) <italic>AtWRKY29</italic> (At4g23550) and (<bold>E</bold>) <italic>AtWRKY30</italic> (At5g24110) gene expression was analyzed using qRT-PCR in the wild-type, <italic>Atcerk1</italic> and <italic>Atlyk5-2</italic> mutant plants with or without treatment with chitooctaose, 8mer. <italic>UBQ10</italic> (At4g05320) was used a control. Data are mean ± SE (n = 3). Asterisks indicate significant difference relative to H<sub>2</sub>O treated Col-0 wild-type plants. (p &lt; 0.01, Student's <italic>t</italic> test). (<bold>F</bold>) 4-week-old leaves from Col-0 wild-type, <italic>Atcerk1</italic>, <italic>Atlyk5-2</italic>, and <italic>Atlyk4/lyk5-2</italic> mutant plants were inoculated with <italic>Alternaria brassicicola</italic> 24 hr after hand-infiltration with H<sub>2</sub>O or 1 µM chitooctaose. The diameter of the lesion area was measured 4 days after inoculation. Data are mean ± SE (n = 12). Asterisks indicate significant difference relative to H<sub>2</sub>O treated Col-0 wild-type plants. (p &lt; 0.05, Student's <italic>t</italic> test). (<bold>G</bold>) Leaf populations of <italic>Psuedomonas syringae</italic> pv. tomato DC3000 3 days after inoculation. 4-week-old plants were either pretreated with H<sub>2</sub>O or 1 µM chitooctaose 24 hr before inoculation with <italic>P. syringae</italic>. Data are mean ± SE (n = 9). Asterisk indicates T-test significant difference compared with H<sub>2</sub>O-treated Col-0 plants at p &lt; 0.05, Student's <italic>t</italic> test. (<bold>H</bold>) <italic>AtCERK1, AtLYK4</italic> and <italic>AtLYK5</italic> gene expression in different plant ages and plant tissue. RNA from whole seedling of 5 day, 10 day, 20 day old plants and leaf and root tissues from 20 day old plants were used for reverse transcript and qRT-PCR was performed using specific primers. Data are mean ± SE (n = 3). Asterisks indicate significant difference relative to chitiooctaose treated Col-0 wild-type plants (p &lt; 0.01, Student's <italic>t</italic> test).</p><p><bold>DOI:</bold> <ext-link ext-link-type="doi" xlink:href="10.7554/eLife.03766.003">http://dx.doi.org/10.7554/eLife.03766.003</ext-link></p></caption><graphic xlink:href="elife03766f001"/></fig><fig id="fig1s1" position="float" specific-use="child-fig"><object-id pub-id-type="doi">10.7554/eLife.03766.004</object-id><label>Figure 1—figure supplement 1.</label><caption><title>Arabidopsis LYK gene family.</title><p>A complete alignment based on the full-length sequences of each protein was used to draw the phylogenetic tree using Clustal X software. AtCERK1: At3g21630, AtLYK2: At3g01840, AtLYK3: At1g51940, AtLYK4: At2g23770, AtLYK5: At2g33580.</p><p><bold>DOI:</bold> <ext-link ext-link-type="doi" xlink:href="10.7554/eLife.03766.004">http://dx.doi.org/10.7554/eLife.03766.004</ext-link></p></caption><graphic xlink:href="elife03766fs001"/></fig><fig id="fig1s2" position="float" specific-use="child-fig"><object-id pub-id-type="doi">10.7554/eLife.03766.005</object-id><label>Figure 1—figure supplement 2.</label><caption><title>Chitin response in Ler <italic>lyk5-1</italic> mutant plants.</title><p>(<bold>A</bold>–<bold>B</bold>) <italic>WRKY53</italic> gene (<bold>A</bold>) and <italic>WRKY33</italic> gene (<bold>B</bold>) expression was analyzed using qRT-PCR in Ler wild-type and <italic>Atlyk5-1</italic> mutant plants with or without treatment with 1 µM chitooctaose. 8mer: chitooctaose. Data are ± SE (n = 3), *p &lt; 0.05. (<bold>C</bold>–<bold>D</bold>) MPK phosphorylation in Ler wild-type and Atlyk5-1 mutant plants revealed by immunoblot. Leaf discs from 5-week-old plants (<bold>C</bold>) or 2-week-old seedlings (<bold>D</bold>) were subjected to the treatment with 1 µM chitooctaose for the time point shown in figures. Lower panel shows similar loading of total protein. (<bold>E</bold>) Chitin induces AtCERK1 phosphorylation. Mature leaves from Col-0 wild type plants were hand-infiltrated with 1 µM chitooctaose or H<sub>2</sub>O as control for 15 min. All samples were incubated with antarctic phosphatase or H<sub>2</sub>O as control at 37°C for 15 min. Anti-AtCERK1 antibody was used to detect AtCERK1 protein. (<bold>F</bold>) AtCERK1 phosphorylation in Ler wild-type and <italic>Atlyk5-1</italic> mutant plants revealed by immunoblot using anti-AtCERK1 antibody after hand-infiltration with 1 µM chitooctaose for the time points shown in figures. (<bold>G</bold>) ROS production was measured from the Ler wild-type plants, <italic>Atlyk5-1</italic> mutant plants, Col-0 wild-type plants, <italic>Atlyk5-2</italic> mutant plants for 30 min after treatment with 0.5 µM chitooctaose. Data are mean ± SE (n = 6). Asterisk indicates significant difference. (p &lt; 0.01, Student's <italic>t</italic> test).</p><p><bold>DOI:</bold> <ext-link ext-link-type="doi" xlink:href="10.7554/eLife.03766.005">http://dx.doi.org/10.7554/eLife.03766.005</ext-link></p></caption><graphic xlink:href="elife03766fs002"/></fig><fig id="fig1s3" position="float" specific-use="child-fig"><object-id pub-id-type="doi">10.7554/eLife.03766.007</object-id><label>Figure 1—figure supplement 3.</label><caption><title>Characterization of <italic>Atlyk5</italic> mutant plants.</title><p>(<bold>A</bold>) Genomic structure of <italic>AtLYK5</italic> and two insertion sites of two mutants. (<bold>B</bold>) Identification of T-DNA insertion by PCR using genomic DNA from Col-0 wild-type and <italic>Atlyk5-2</italic> mutant plants. Location of primers used is shown in (<bold>A</bold>). Primer sequences are listed in <xref ref-type="supplementary-material" rid="SD1-data">Supplemental file 1</xref>. (<bold>C</bold>) RT-PCR was used to identify transcriptional expression of <italic>AtLYK5</italic> in Col-0 WT and <italic>Atlyk5-2</italic> mutant plants. Upper panel shows expression level of <italic>AtLYK5</italic> in Col-0 and <italic>Atlyk5-2</italic> mutant plants, lower panel shows expression of <italic>AtCERK1</italic> as a control.</p><p><bold>DOI:</bold> <ext-link ext-link-type="doi" xlink:href="10.7554/eLife.03766.007">http://dx.doi.org/10.7554/eLife.03766.007</ext-link></p></caption><graphic xlink:href="elife03766fs003"/></fig><fig id="fig1s4" position="float" specific-use="child-fig"><object-id pub-id-type="doi">10.7554/eLife.03766.008</object-id><label>Figure 1—figure supplement 4.</label><caption><title><italic>WRKY33</italic> and <italic>WRKY53</italic> gene expression in <italic>Atlyk5-2</italic> mutant plants.</title><p>(<bold>A</bold>) Calcium influx in the wild-type, <italic>Atcerk1</italic> and <italic>Atlyk5-2</italic> mutant plants expressing aequorin was recorded for 30 min after 100 nM flg22 treatment. (<bold>B</bold>) <italic>WRKY33</italic> (At2g38470) and (<bold>C</bold>) <italic>WRKY53</italic> (At4g23810) gene expression was analyzed using qRT-PCR in the wild-type, <italic>Atcerk1</italic> and <italic>Atlyk5-2</italic> mutant plants with or without treatment with chitooctaose, 8mer. <italic>UBQ10</italic> (At4g05320) was used a control. Data are mean ± SE (n = 3). Asterisks indicate significant difference relative to chitiooctaose treated Col-0 wild-type plants (p &lt; 0.01, Student's <italic>t</italic> test).</p><p><bold>DOI:</bold> <ext-link ext-link-type="doi" xlink:href="10.7554/eLife.03766.008">http://dx.doi.org/10.7554/eLife.03766.008</ext-link></p></caption><graphic xlink:href="elife03766fs004"/></fig><fig id="fig1s5" position="float" specific-use="child-fig"><object-id pub-id-type="doi">10.7554/eLife.03766.006</object-id><label>Figure 1—figure supplement 5.</label><caption><title>Chitin-induced ROS production in five <italic>lyk</italic> mutant plants.</title><p>ROS production was measured from Col-0 wild-type, five <italic>Atlyk</italic> mutant, and <italic>Atlyk4</italic>/<italic>Atlyk5-2</italic> double mutant plants for 30 min after treatment with 1 µM chitooctaose. Data are mean ± SE (n = 8). Asterisks indicate significant difference relative to chitooctaose treated Col-0 wild-type plants. (p &lt; 0.01, Student's <italic>t</italic> test).</p><p><bold>DOI:</bold> <ext-link ext-link-type="doi" xlink:href="10.7554/eLife.03766.006">http://dx.doi.org/10.7554/eLife.03766.006</ext-link></p></caption><graphic xlink:href="elife03766fs005"/></fig></fig-group></p></sec><sec id="s2-2"><title>AtLYK5 shares overlapping function with AtLYK4 in mediating the chitin response</title><p>Analysis of the <italic>Atlyk5</italic> mutant plants showed some residual response to chitin. Previously, we reported that AtLYK4 is also required for chitin elicitation (<xref ref-type="bibr" rid="bib58">Wan et al., 2012</xref>). Phylogenetic analysis shows that AtLYK5 and AtLYK4 are in the same branch (<xref ref-type="fig" rid="fig1s1">Figure 1—figure supplement 1</xref>). Therefore, we examined the possibility that AtLYK4 may provide some functional redundancy for the loss of AtLYK5; thus, explaining the low level response of the <italic>Atlyk5</italic> mutants to chitin. To address this hypothesis, mutant plants defective in both AtLYK4 and AtLYK5 were generated through crossing (<xref ref-type="fig" rid="fig2s1">Figure 2—figure supplement 1</xref>) and tested for their response to chitin. Similar to the <italic>Atcerk1</italic> mutants, plants mutated in AtLYK4 and AtLYK5 lost all tested responses to chitin, including ROS production and MAPK phosphorylation, as well as resistance to the fungal pathogen <italic>A. brassicicola</italic> (<xref ref-type="fig" rid="fig1">Figure 1F</xref> and <xref ref-type="fig" rid="fig2">Figure 2</xref>). These genetic studies suggest that AtLYK5 and AtCERK1 are essential for a strong plant chitin response, while AtLYK4 can partially compensate for the loss of AtLYK5.<fig-group><fig id="fig2" position="float"><object-id pub-id-type="doi">10.7554/eLife.03766.009</object-id><label>Figure 2.</label><caption><title>AtLYK5 has overlapping function with AtLYK4.</title><p>(<bold>A</bold>) ROS production was measured from Col-0 wild-type, <italic>Atyk4</italic>, <italic>Atlyk5</italic>-2, and <italic>Atlyk4/lyk5</italic>-2 mutant plants for 30 min after treatment with H<sub>2</sub>O (as control) or 1 µM chiooctaose. 8mer: chitooctaose. Data are mean ± SE (n = 8). (<bold>B</bold>) and (<bold>C</bold>) Western blot of total protein extracts from plants treated with 1 µM chitooctaose. Protein was separated by SDS-PAGE gel and visualized using anti-P44/P42 antibody. Upper panel in each figure shows phosphorylated MPK3 and MPK6, lower panel shows similar loading of each lane stained with ponceau S solution.</p><p><bold>DOI:</bold> <ext-link ext-link-type="doi" xlink:href="10.7554/eLife.03766.009">http://dx.doi.org/10.7554/eLife.03766.009</ext-link></p></caption><graphic xlink:href="elife03766f002"/></fig><fig id="fig2s1" position="float" specific-use="child-fig"><object-id pub-id-type="doi">10.7554/eLife.03766.010</object-id><label>Figure 2—figure supplement 1.</label><caption><title>Complementation of <italic>Atlyk5-2</italic> mutant plants.</title><p>(<bold>A</bold>) HA-tagged AtLYK5 protein levels in different transgenic <italic>Atlyk5-2</italic> mutant plants expressing full length <italic>AtLYK5</italic> under the control of its native promoter. (<bold>B</bold>) ROS production was measured from the wild type plants, and <italic>Atlyk5-2</italic> mutant plants, and the <italic>Atlyk5-2</italic> mutant plants expressing <italic>AtLYK5</italic> under the control of its native promoter for 30 min after chitooctaose. <italic>AtLYK5</italic> indicates complementation lines (#1 and #3 were used). Data are mean ± SE (n = 8). Asterisks indicate significant difference relative to H<sub>2</sub>O treated Col-0 wild type plants. (p &lt; 0.01, Student's <italic>t</italic> test). (<bold>C</bold>) MPK phosphorylation in different transgenic plants shown above prior (−) or 15 min (+) after 1 µM chitooctaose treatment detected using anti-P44/P42 antibody. Lower panel shows similar loading of each lane stained with ponceau S solution. #1 and #3 indicate two different transgenic plants expressing <italic>AtLYK5</italic> in <italic>Atlyk5-2</italic> mutant plants. (<bold>D</bold>) Identification of <italic>Atlyk4</italic>/<italic>Atlyk5-2</italic> double knockout mutant plants. Whole genomic DNA was extracted from <italic>Atlyk4</italic><sup><italic>+/−</italic></sup>/<italic>Atlyk5-2</italic><sup><italic>+/−</italic></sup> and <italic>Atlyk4</italic><sup><italic>−/−</italic></sup><italic>/Atlyk5-2</italic><sup><italic>−/−</italic></sup> mutant plants. PCR was used to characterize homozygous <italic>Atlyk4/Atlyk5-2</italic> double mutant plants. Primer pairs used as following: 1 and 3: AtLYK4 LP + AtLYK4 RP, 2 and 4: AtLYK4 LB + AtLYK5 RP, 5 and 7: AtLYK5 LP + AtLYK5 RP, 6 and 8: AtLYK5 LB + AtLYK5 RP.</p><p><bold>DOI:</bold> <ext-link ext-link-type="doi" xlink:href="10.7554/eLife.03766.010">http://dx.doi.org/10.7554/eLife.03766.010</ext-link></p></caption><graphic xlink:href="elife03766fs006"/></fig><fig id="fig2s2" position="float" specific-use="child-fig"><object-id pub-id-type="doi">10.7554/eLife.03766.011</object-id><label>Figure 2—figure supplement 2.</label><caption><title>Tissue-specific expression of <italic>AtCERK1</italic>, <italic>AtLYK4</italic>, and <italic>AtLYK5</italic>.</title><p>(<bold>A</bold>) <italic>AtCERK1</italic> (At3g21630), <italic>AtLYK4</italic> (At2g23770) and <italic>AtLYK5</italic> (At2g33580) gene expression in different developmental stages predicted by AtGenExpress Visualization Tool (AVT) . Results can also be seen at <ext-link ext-link-type="uri" xlink:href="http://jsp.weigelworld.org/expviz/expviz.jsp">http://jsp.weigelworld.org/expviz/expviz.jsp</ext-link>. (<bold>B</bold>) Subcellular localization of AtLYK5 in <italic>Nicotiana bethamiana</italic>. Leaf expressing AtLYK5-GFP was stained with FM4-64 before monitoring epifluorescence signal using confocal microscopy (Left panel). Right panel showed expression of AtLYK5-GFP detected by immunoblot using anti-GFP.</p><p><bold>DOI:</bold> <ext-link ext-link-type="doi" xlink:href="10.7554/eLife.03766.011">http://dx.doi.org/10.7554/eLife.03766.011</ext-link></p></caption><graphic xlink:href="elife03766fs007"/></fig></fig-group></p><p>Because AtCERK1, AtLYK5, and AtLYK4 are all involved in the chitin response, we measured their transcriptional level in different plant tissues at different plant ages using quantitative PCR (qRT-PCR). At different growth stages of 5, 10, and 20 days after germination, as well as leaf and root tissues from 20-day-old plants, the transcript levels of three genes were similar. However, in the root tissue tested, <italic>AtLYK5</italic> expression was higher than <italic>AtCERK1</italic> and <italic>AtLYK4</italic>, while both showed similar expression levels in roots (<xref ref-type="fig" rid="fig1">Figure 1H</xref>). These data are consistent with the results predicted by the AtGenExpress Visualization Tool (AVT) showing that <italic>AtLYK5</italic> is co-expressed with <italic>AtCERK1</italic>, with some variation in the root (<xref ref-type="fig" rid="fig2s2">Figure 2—figure supplement 2</xref> or online at <ext-link ext-link-type="uri" xlink:href="http://jsp.weigelworld.org/expviz/expviz.jsp">http://jsp.weigelworld.org/expviz/expviz.jsp</ext-link>).</p><p>Previous reports showed that both AtCERK1 and AtLYK4 are localized on the plasma membrane (<xref ref-type="bibr" rid="bib38">Miya et al., 2007</xref>; <xref ref-type="bibr" rid="bib58">Wan et al., 2012</xref>). The AtLYK5 was fused with c-terminal GFP and transiently expressed under the CaMV <italic>35S</italic> promoter in <italic>Nicotiana benthamiana</italic>. Confocal microscopy showed that AtLYK5-GFP co-localized with the plasma membrane dye, FM4-64, and western blots showed the correct size of the AtLYK5-GFP protein (<xref ref-type="fig" rid="fig2s2">Figure 2—figure supplement 2</xref>). These results indicate that together with AtCERK1 and AtLYK4, AtLYK5 is a membrane-localized protein.</p></sec><sec id="s2-3"><title>AtLYK5 binds to chitin with higher affinity than AtCERK1</title><p>Given the low reported affinity of AtCERK1 for chitooctaose (<xref ref-type="bibr" rid="bib32">Liu et al., 2012b</xref>), we tested the ability of AtLYK5 to bind to chitin. HA-tagged versions of each of the five AtLYK proteins were expressed in <italic>Arabidopsis</italic> protoplasts and chitin-magnetic beads were used to pull down any chitin binding proteins. As shown in <xref ref-type="fig" rid="fig3s1">Figure 3—figure supplement 1</xref>, besides AtCERK1, only AtLYK4 and AtLYK5 were also pulled down by chitin beads. The binding with AtLYK5 was strongly inhibited by chitoheptaose and chitooctaose, whereas the binding with AtCERK1 or AtLYK4 was only slightly reduced by the same competitors, consistent with AtLYK5 having a higher binding affinity for chitooctaose relative to AtCERK1.</p><p>In order to further investigate this possibility, the chitin binding ability of the extracellular domains of AtCERK1 and AtLYK5 were measured using isothermal titration calorimetry (ITC). As shown in <xref ref-type="fig" rid="fig3">Figure 3</xref>, the binding affinity of AtLYK5 for chitooctaose was measured (K<sub>d</sub> = 1.72 µM), which is roughly 200-fold higher than measured for AtCERK1 under the same conditions (K<sub>d</sub> = 455 µM) (<xref ref-type="fig" rid="fig3">Figure 3A,B</xref>). In control experiments, no chitin binding affinity was detected using buffer titrated with chitooctaose (<xref ref-type="fig" rid="fig3s1">Figure 3—figure supplement 1</xref>). As expected, AtLYK5 showed no binding affinity for elicitor-inactive chitotetraose (<xref ref-type="fig" rid="fig3s1">Figure 3—figure supplement 1</xref>). As a positive control, wheat germ agglutinin (WGA) showed strong chitin binding affinity (K<sub>d</sub> = 1.6 µM; <xref ref-type="fig" rid="fig3s1">Figure 3—Figure supplement 1</xref>). Therefore, the data indicate that AtCERK1 shows very low affinity for chitooctaose, while AtLYK5 shows an affinity very close to the well-characterized chitin binding protein WGA.<fig-group><fig id="fig3" position="float"><object-id pub-id-type="doi">10.7554/eLife.03766.012</object-id><label>Figure 3.</label><caption><title>AtLYK5 shows stronger chitin binding affinity than AtCERK1.</title><p>The binding affinity of AtLYK5 (<bold>A</bold>) and AtCERK1 (<bold>B</bold>) to chitooctaose (GlcNAc)<sub>8</sub> was measured using isothermal titration calorimetry (ITC). Proteins were purified from <italic>E. coli</italic>. Upper panels and lower panels indicate raw data and integrated heat values, respectively.</p><p><bold>DOI:</bold> <ext-link ext-link-type="doi" xlink:href="10.7554/eLife.03766.012">http://dx.doi.org/10.7554/eLife.03766.012</ext-link></p></caption><graphic xlink:href="elife03766f003"/></fig><fig id="fig3s1" position="float" specific-use="child-fig"><object-id pub-id-type="doi">10.7554/eLife.03766.013</object-id><label>Figure 3—figure supplement 1.</label><caption><title>AtLYK5 has chitooctaose binding affinity.</title><p>(<bold>A</bold>) Chitin binding of AtLYK proteins detected using chitin-magnetic beads. HA-tagged AtCERK1 and AtLYK2-5 were expressed from the <italic>35S</italic> promoter in protoplasts made from Col-0 wild type plants. Protoplasts were treated either with 10 µM of the specific chitin oligomer noted above for 15 min (+) or with H<sub>2</sub>O (−) before harvest. Proteins were pulled-down using chitin magnetic beads (New England Biolabs, Ipswich, MA). Upper panel shows input of each protein, lower panel shows proteins after chitin binding. IB, immnunoblot with anti-HA antibody. (<bold>B</bold>–<bold>C</bold>) Wheat germ agglutinin binds to chitin with high affinity. Binding of wheat germ agglutin in the (<bold>B</bold>) presence of chitin (GlcNAc)<sub>8</sub> or (<bold>C</bold>) buffer. Binding was measured using isothermal titration calorimetry (ITC). Upper panels and (lower panels) indicate raw data and integrated heat values, respectively. (<bold>D</bold>) Binding affinity of AtLYK5 in presence of chitin (GlcNAc)<sub>4</sub>. Binding was measured using isothermal titration calorimetry (ITC). Upper panels and (lower panels) indicate raw data and integrated heat values, respectively.</p><p><bold>DOI:</bold> <ext-link ext-link-type="doi" xlink:href="10.7554/eLife.03766.013">http://dx.doi.org/10.7554/eLife.03766.013</ext-link></p></caption><graphic xlink:href="elife03766fs008"/></fig></fig-group></p></sec><sec id="s2-4"><title>Tyr-128 and Ser-206 residues are important for the AtLYK5-mediated chitin response</title><p>The AtCERK1 crystal structure predicted chitooctaose binding to the second LysM motif of the extracellular domain leading to homodimerization and kinase activation (<xref ref-type="bibr" rid="bib32">Liu et al., 2012b</xref>). However, AtCERK1 appears to be a very weak chitin binding protein raising questions as to the biological relevance of the AtCERK1 homodimer model. Therefore, in order to predict the chitin binding site(s) within the AtLYK5 extracellular domain, a computational model of the AtLYK5 ectodomain was built by homology modeling against the known crystal structure of the fungal ECP6 (<xref ref-type="bibr" rid="bib47">Sanchez-Vallet et al., 2013</xref>), a LysM effector protein, which binds chitin with very high affinity (binding at pM levels; <xref ref-type="fig" rid="fig4">Figure 4A,B</xref> and <xref ref-type="fig" rid="fig4s1">Figure 4—figure supplement 1</xref>). Based on the docking model of AtLYK5 with chitooctaose, the binding affinity was calculated at −8.9 kcal mol<sup>−1</sup> (<xref ref-type="fig" rid="fig4">Figure 4A,B</xref>), a value comparable to the computational binding affinity of ECP6 (−9.0 kcal mol<sup>−1</sup>) (<xref ref-type="fig" rid="fig4s1">Figure 4—figure supplement 1</xref>). Four residues, that is, Thr-72, Tyr-128, Ser-206, and Ser-216, were predicted to form hydrogen bonds and hydrophobic interactions with chitooctaose based on docking model (<xref ref-type="fig" rid="fig4s1">Figure 4—figure supplement 1</xref>). Point mutations were introduced at each of these residues and transgenically expressed in <italic>Atlyk5</italic> mutant plants from the native promoter. As shown in <xref ref-type="fig" rid="fig4">Figure 4C</xref>, <italic>AtLYK5</italic><sup><italic>S206P</italic></sup> and <italic>AtLYK5</italic><sup><italic>Y128G</italic></sup> transgenic plants could not rescue the <italic>Atlyk5-2</italic> mutant phenotype as measured by chitin-triggered ROS production. In contrast, expression of AtLYK5<sup>T72G</sup> and AtLYK5<sup>S216P</sup> mutant proteins in the <italic>Atlyk5-2</italic> mutant plants did restore the chitin response. Consistent with these results, AtLYK5<sup>S206P</sup> mutant proteins did not bind to chitin beads, while AtLYK5<sup>Y128G</sup> mutant proteins showed a strong reduction in chitin binding using this same assay (<xref ref-type="fig" rid="fig4">Figure 4D</xref>). Binding of the AtLYK5<sup>T72G</sup> and AtLYK5<sup>S216P</sup> mutant proteins to the chitin beads was similar to wild-type AtLYK5 (<xref ref-type="fig" rid="fig4">Figure 4D</xref>). These data indicate that residues Tyr-128 and Ser-206 of AtLYK5 are important for chitin binding and that chitin binding is essential for biological activity.<fig-group><fig id="fig4" position="float"><object-id pub-id-type="doi">10.7554/eLife.03766.014</object-id><label>Figure 4.</label><caption><title>Tyr-128 and Ser-206 are important for AtLYK5-mediated chitin response.</title><p>(<bold>A</bold>) A computational ribbon structure of the AtLYK5 ectodomain was built based on crystal structure of fungal ECP6. The model shows the three AtLYK5 LysM domains, i.e. LysM1-3. Each LysM domain contains two beta strands and two helixes interconnected via loops. (<bold>B</bold>) The binding affinity was calculated at −8.9 kcal mol<sup>−1</sup>. The binding site was formed by 3 LysM motifs. Green lines depict hydrogen bonds formed between ligand atoms and their corresponding residues atoms. (<bold>C</bold>) Reactive oxygen species (ROS) was measured within 30 min after chitin treatment. The <italic>AtLYK5</italic> wild-type gene or versions with specific point mutations were transformed into <italic>Atlyk5-2</italic> mutant plants. Eight individual transgenic plants were used for this measurement. Data are mean ± SE. Asterisks indicate significant difference relative to H<sub>2</sub>O treated Col-0 wild-type plants. (p &lt; 0.01, Student's <italic>t</italic> test). (<bold>D</bold>) Chitin binding affinity of AtLYK5 and AtLYK5 mutant proteins as labeled in (<bold>C</bold>) detected by anti-HA antibody. Upper panel shows input of each transgenic plant, lower panel shows western blot after pull down with chitin-magnetic beads.</p><p><bold>DOI:</bold> <ext-link ext-link-type="doi" xlink:href="10.7554/eLife.03766.014">http://dx.doi.org/10.7554/eLife.03766.014</ext-link></p></caption><graphic xlink:href="elife03766f004"/></fig><fig id="fig4s1" position="float" specific-use="child-fig"><object-id pub-id-type="doi">10.7554/eLife.03766.015</object-id><label>Figure 4—figure supplement 1.</label><caption><title>Computational model of the extracellular domain of AtLYK5.</title><p>(<bold>A</bold>–<bold>C</bold>) The docking model of the ectodomain with chitooctaose shown in surface (<bold>A</bold>) and ribbon form (<bold>B</bold>) and a close-up surface (<bold>C</bold>). The binding affinity was calculated at −8.9 kcal mol<sup>−1</sup>. The model shows the three AtLYK5 LysM domains, that is, LysM1-3. Each LysM domain contains two beta strands and two helixes interconnected via loops. (<bold>D</bold>–<bold>E</bold>) Docking of chitooctaose to the ECP6. (<bold>D</bold>) A ribbon structure represents the docking model of ECP6 (gray color) and chitooctaose (blue, red and yellow sticks). The binding affinity was calculated at −9.0 kcal mol<sup>−1</sup>. (<bold>E</bold>) A molecular surface of ECP6 with chitooctaose binding site formed by 3 LysM motifs.</p><p><bold>DOI:</bold> <ext-link ext-link-type="doi" xlink:href="10.7554/eLife.03766.015">http://dx.doi.org/10.7554/eLife.03766.015</ext-link></p></caption><graphic xlink:href="elife03766fs009"/></fig></fig-group></p></sec><sec id="s2-5"><title>The association between AtLYK5 and AtCERK1 is induced by chitin elicitation</title><p>Given that both AtCERK1 and AtLYK5 are required for a strong chitin response, we hypothesized that AtLYK5 might interact with AtCERK1. Indeed, co-immunoprecipitation (Co-IP) assays showed that AtCERK1-HA strongly interacts with AtLYK5-Myc in the presence of chitin (<xref ref-type="fig" rid="fig5">Figure 5A</xref>). Chitin-induced association between AtLYK5 and AtCERK1 was much stronger than homodimerization of AtCERK1 (<xref ref-type="fig" rid="fig5">Figure 5A</xref>). We also tested the chemical specificity of this response using chitin oligomers of increasing length (<xref ref-type="fig" rid="fig5">Figure 5B</xref>). Chitopentaose which can not trigger immune responses in plants did not induce AtLYK5-CERK1 association, while chitin oligomers (dp ≥ 6), which are strong elicitors, induced the interaction between AtLYK5 and AtCERK1 (<xref ref-type="fig" rid="fig5">Figure 5B</xref>). We also tested the association between AtLYK4 and AtCERK1 before and after chitin treatment. As shown in <xref ref-type="fig" rid="fig5s1">Figure 5—figure supplement 1</xref>, AtCERK1-HA could be co-immunoprecipitated with AtLYK4-Myc; however, this interaction was independent of the presence of chitin.<fig-group><fig id="fig5" position="float"><object-id pub-id-type="doi">10.7554/eLife.03766.016</object-id><label>Figure 5.</label><caption><title>AtLYK5 regulates chitin-induced phosphorylation and homodimerization of AtCERK1.</title><p>(<bold>A</bold>) AtLYK5 associates with AtCERK1 after chitin treatments. HA-tagged AtCERK1 and Myc-tagged AtLYK5 or AtCERK1 were co-expressed in protoplasts made from Col-0 wild-type plants. Protoplasts were harvested with or without the treatment with 1 µM chitooctaose as labeled above. Co-immunoprecipitation was made using anti-Myc antibody. Left panel and right panel are cropped from the same gel. (<bold>B</bold>) The association between AtCERK1 and AtLYK5 is induced by different chitin oligomers. Protoplasts were treated with different chitin oligomers (1 µM) as shown above for 15 min. (<bold>C</bold>) AtLYK5 regulates chitin-induced AtCERK1-AtCERK1 association. HA-tagged AtCERK1 and Myc-tagged AtCERK1 were copexpressed in protoplasts made from Col-0 wild-type or <italic>Atlyk5-2</italic> mutant plants. Protoplasts were harvested with or without the treatment with 1 µM chitooctaose. Co-immunoprecipitation was made using anti-Myc antibody. (<bold>D</bold>) AtLYK5 controls chitin-induced phosphorylation of AtCERK1. Plant leaves from wild-type and the <italic>Atlyk5-2</italic> mutant plants were treated with 1 µM chitooctaose for the time shown above. Anti-AtCERK1 antibody was used to detect the phosphorylation status of AtCERK1 shown as a shift in protein migration. Lower panel shows a non-specific band used to assess similar loading of each lane.</p><p><bold>DOI:</bold> <ext-link ext-link-type="doi" xlink:href="10.7554/eLife.03766.016">http://dx.doi.org/10.7554/eLife.03766.016</ext-link></p></caption><graphic xlink:href="elife03766f005"/></fig><fig id="fig5s1" position="float" specific-use="child-fig"><object-id pub-id-type="doi">10.7554/eLife.03766.017</object-id><label>Figure 5—figure supplement 1.</label><caption><title>AtLYK4 associates with AtCERK1 before and after chitin treatment.</title><p>(<bold>A</bold>) Interaction between AtCERK1 and AtLYK4. HA-tagged AtCERK1 and Myc-tagged AtLYK4 were co-expressed in protoplasts from Col-0 wild type plants. Protoplasts either prior (−) or after treatment with 1 µM chitooctaose were harvested. Co-immunoprecipitation used anti-Myc antibody. IB, immunoblot detected with either anti-HA or anti-Myc antibodies. (<bold>B</bold>) Chitin-induced phopshorylation of AtCERK1. Mature leaves from Col-0 wild-type, <italic>Atlyk4</italic>, and <italic>Atlyk5-2</italic> mutant plants were treated with 1 µM chitin oligomers for 15 min. Total protein was separated on 7% SDS-PAGE and immunoblots were detected with anti-AtCERK1 antibody. Protein band shift indicates phosphorylation. 6mer: chitohexaose, 7mer: chitoheptaose, and 8mer: chitooctaose. Upper panel shows immunoblot probed with anti-AtCERK1 antibody, lower panel shows a non-specific band detected by anti-AtCERK1 antibody as a loading control.</p><p><bold>DOI:</bold> <ext-link ext-link-type="doi" xlink:href="10.7554/eLife.03766.017">http://dx.doi.org/10.7554/eLife.03766.017</ext-link></p></caption><graphic xlink:href="elife03766fs010"/></fig></fig-group></p></sec><sec id="s2-6"><title>AtLYK5 is necessary for chitin-induced AtCERK1 phosphorylation and homodimerization</title><p>Previously, it was postulated that chitin-induced AtCERK1 homodimerization leads to AtCERK1 phosphorylation (<xref ref-type="bibr" rid="bib32">Liu et al., 2012b</xref>; <xref ref-type="bibr" rid="bib44">Petutschnig et al., 2010</xref>), required for downstream activation of plant innate immunity. Consistent with this model, co-immunoprecipitation demonstrated AtCERK1 dimerization upon chitin addition in wild-type plants (<xref ref-type="fig" rid="fig5">Figure 5C</xref>). However, this association disappeared in the <italic>Atlyk5-2</italic> mutant plants (<xref ref-type="fig" rid="fig5">Figure 5C</xref>). Chitin-induced phosphorylation of AtCERK1 was detected as a protein mobility-shift on SDS-PAGE gels. In contrast, no phosphorylation of AtCERK1 was detected after chitin elicitation of <italic>Atlyk5-2</italic> mutant plants (<xref ref-type="fig" rid="fig5">Figure 5D</xref> and <xref ref-type="fig" rid="fig5s1">Figure 5—figure supplement 1</xref>). These data clearly demonstrate that AtLYK5 is essential for both AtCERK1 dimerization and subsequent activation of protein phosphorylation.</p></sec><sec id="s2-7"><title>The AtLYK5 kinase domain is inactive but is required for chitin-induced association with AtCERK1</title><p>A comparison was made using the amino acid sequences of the intracellular kinase domain of AtLYK5 and other known receptor kinases, including AtCERK1 (<xref ref-type="bibr" rid="bib38">Miya et al., 2007</xref>; <xref ref-type="bibr" rid="bib59">Wan, et al., 2008</xref>), AtBRI1 (<xref ref-type="bibr" rid="bib25">Li and Chory, 1997</xref>), AtBAK1 (<xref ref-type="bibr" rid="bib26">Li et al., 2002</xref>; <xref ref-type="bibr" rid="bib41">Nam and Li, 2002</xref>), AtLYK4 (<xref ref-type="bibr" rid="bib58">Wan et al., 2012</xref>), and Does not Respond to Nucleotides 1 (AtDORN1) (<xref ref-type="bibr" rid="bib10">Choi et al., 2014</xref>). The analysis showed that several residues generally considered essential for kinase activity are missing from the AtLYK5 sequence (<xref ref-type="fig" rid="fig6s1">Figure 6—figure supplement 1</xref>), including those in the P-loop sub-domain I, RD domain in sub-domain VIa, and DFG domain in sub-domain VII (<xref ref-type="fig" rid="fig6s1">Figure 6—figure supplement 1</xref>), suggesting that AtLYK5 lacks kinase activity (<xref ref-type="bibr" rid="bib16">Hanks et al., 1988</xref>). In order to test this directly, the AtLYK5 kinase domain was expressed and purified from <italic>Escherichia coli</italic> and used in an in vitro kinase assay. As shown in <xref ref-type="fig" rid="fig6">Figure 6A</xref>, as a positive control, the AtCERK1 kinase domain showed strong kinase activity as previously reported (<xref ref-type="bibr" rid="bib38">Miya et al., 2007</xref>), while no kinase activity was detected using the AtLYK5 kinase domain. In order to investigate the role of AtLYK5 kinase activity in vivo, wild-type AtLYK5, a mutant AtLYK5<sup>K395E</sup> (mutation of Lys to Glu predicted to disrupt ATP binding ability), and mutant AtLYK5<sup>ΔKD</sup> (deletion of kinase domain) proteins were transgenically expressed in <italic>Atlyk5-2</italic> mutant plants from the native promoter (<xref ref-type="fig" rid="fig6s1">Figure 6—figure supplement 1</xref>). The data show that expression of AtLYK5 or AtLYK5<sup>K395E</sup> could complement the <italic>Atlyk5-2</italic> mutant phenotype, as measured by chitin-triggered ROS production, MAPK phosphorylation, and AtCERK1 phosphorylation, whereas transgenic expression of AtLYK5<sup>ΔKD</sup> did not complement the <italic>Atlyk5-2</italic> mutant (<xref ref-type="fig" rid="fig6">Figure 6B–E</xref>). These results indicate that although AtLYK5 kinase activity is not required for chitin signaling, the intracellular kinase does have a function, which may include mediating protein–protein interactions. Indeed, the AtLYK5<sup>ΔKD</sup> mutant protein could not be co-immunoprecipitated with AtCERK1 after chitin treatment, while AtCERK1 interacted with AtLYK5<sup>K395E</sup> and wild-type AtLYK5 normally (<xref ref-type="fig" rid="fig6">Figure 6F</xref>). These data strongly demonstrate that the kinase domain of AtLYK5 is necessary for the association of AtLYK5 and AtCERK1.<fig-group><fig id="fig6" position="float"><object-id pub-id-type="doi">10.7554/eLife.03766.018</object-id><label>Figure 6.</label><caption><title>The kinase domain of AtLYK5 is critical for chitin signaling.</title><p>(<bold>A</bold>) In vitro kinase activities of AtCERK1 (255–617 aa) and AtLYK5 (309–664 aa) were measured by incorporation of γ-[<sup>32</sup>P]-ATP. Left panel shows autoradiography, and right panel shows gel stained with coomassie brilliant blue. (<bold>B</bold>–<bold>F</bold>) Plant tissues were harvested before (−) or 15 min after (+) treatment or at the time point shown in each figure of treatment with 1 µM chitooctaose. (<bold>B</bold>–<bold>E</bold>) AtLYK5<sup>K395E</sup> but not AtLYK5<sup>ΔKD</sup> (1–320 aa) complemented the <italic>Atlyk5-2</italic> mutant as determined by chitin-triggered ROS production. Asterisks indicate significant difference relative to H<sub>2</sub>O treated Col-0 wild-type plants. (Data are mean ± SE (n = 8), p &lt; 0.01, Student's <italic>t</italic> test), MPK phosphorylation, and chitin-induced AtCERK1 phosphorylation. Upper panel of each figure show immunoblot data, lower panel shows either rubisco band stained with ponceau S solution (<bold>C</bold> and <bold>D</bold>) or a non-specific band (<bold>E</bold>) to show similar loading of each lane. Plant tissues were harvested before (−) or after (+) 15 min treatment with 1 µM chitooctaose. (<bold>F</bold>) AtLYK5<sup>K395E</sup> but not AtLYK5<sup>ΔKD</sup> coimmunoprecipitates with AtCERK1 after chitin elicitation. Co-IP was made using anti-AtCERK1 antibody with proteins from transgenic Arabidopsis <italic>Atlyk5-2</italic> mutant plants expressing either AtLYK5, or AtLYK5<sup>K395E</sup> or AtLYK5<sup>ΔKD</sup>. 8mer: chitooctaose, <italic>AtLYK5</italic>, <italic>K395E</italic>, and <italic>ΔKD</italic> indicate transgenic Arabidopsis expressing AtLYK5, AtLYK5<sup>K395E</sup>, and AtLYK5<sup>ΔKD</sup>, respectively. Different number indicates different transgenic lines used in this study.</p><p><bold>DOI:</bold> <ext-link ext-link-type="doi" xlink:href="10.7554/eLife.03766.018">http://dx.doi.org/10.7554/eLife.03766.018</ext-link></p></caption><graphic xlink:href="elife03766f006"/></fig><fig id="fig6s1" position="float" specific-use="child-fig"><object-id pub-id-type="doi">10.7554/eLife.03766.019</object-id><label>Figure 6—figure supplement 1.</label><caption><title>AtLYK5 is a kinase inactive protein.</title><p>(<bold>A</bold>) AtLYK5 lacks conserved residues required for kinase activity. Sequence alignment was done using the entire intracellular domain of AtLYK5 and other, selected receptor kinases. Each kinase subdomain is labeled by as Roman numeral and the conserved residues of each subdomain are shown below these numbers. Amino acids sequences of each kinase used for alignment are shown as following: AtBAK1 (At4g33430): 297–662 aa, AtBRI1 (At4g39400): 815–1196 aa, AtDORN1 (At5g60300): 310–718 aa, AtLYK5 (At2g33580): 301–664 aa, AtLYK4 (At2g23770): 295–612 aa, AtCERK1 (At3g21630): 255–671 aa. (<bold>B</bold>–<bold>C</bold>) Expression of AtLYK5<sup>K395E</sup> (<bold>B</bold>) and AtLYK5<sup>ΔKD</sup> (<bold>C</bold>) with a C-terminal HA tag from the native promoter in <italic>Atlyk5-2</italic> mutant plants. Upper panel shows protein level detected using anti-HA antibody, lower panel shows similar loading of each lane stained with ponceau S solution. AtLYK5<sup>ΔKD</sup>: 1–320 aa.</p><p><bold>DOI:</bold> <ext-link ext-link-type="doi" xlink:href="10.7554/eLife.03766.019">http://dx.doi.org/10.7554/eLife.03766.019</ext-link></p></caption><graphic xlink:href="elife03766fs011"/></fig></fig-group></p></sec><sec id="s2-8"><title>AtLYK5 homodimerizes before and after chitin elicitation</title><p>Receptor homodimerization or oligomerization is a common mechanism for ligand-mediate receptor activation (<xref ref-type="bibr" rid="bib20">Jiang and Hunter, 1999</xref>; <xref ref-type="bibr" rid="bib37">Mellado et al., 2001</xref>; <xref ref-type="bibr" rid="bib42">Pang and Zhou, 2013</xref>; <xref ref-type="bibr" rid="bib52">Stock, 1996</xref>). Therefore, we tested whether AtLYK5 could form homodimers and whether this required AtCERK1 and/or chitin treatment. As shown in <xref ref-type="fig" rid="fig7">Figure 7</xref>, AtLYK5 homodimers were detected even in the absence of chitin and this association was independent of the presence of AtCERK1 (<xref ref-type="fig" rid="fig7">Figure 7A</xref>). AtLYK5 homodimers were also detected in vivo (<xref ref-type="fig" rid="fig7">Figure 7B</xref>). In the presence of dithiothreitol, a reducing reagent that disrupts disulfide bonds, AtLYK5 proteins became monomers (<xref ref-type="fig" rid="fig7">Figure 7B</xref>). In addition, we did not observe any molecules larger than AtLYK5 dimers, suggesting no oligomerization of AtLYK5 (<xref ref-type="fig" rid="fig7">Figure 7B</xref>).<fig-group><fig id="fig7" position="float"><object-id pub-id-type="doi">10.7554/eLife.03766.020</object-id><label>Figure 7.</label><caption><title>AtLYK5 forms a homodimer.</title><p>(<bold>A</bold>) Homodimeriztion of AtLYK5 is independent on the presence of CERK1 or chitin elicitation. AtLYK5-HA and AtLYK5-Myc, or AtCERK1-HA and AtCERK1-Myc were co-expressed in protoplasts made from Col-0 and <italic>Atcerk1</italic> mutant plants. Protoplasts were harvested before (−) or 15 min after (+) treatment with 1 µM different chitin oligomers. Co-immunoprecipitation was made using anti-Myc antibody. (<bold>B</bold>) Dithiothreitol (DTT) treatment converts AtLYK5 dimer to monomer. Crude protein was extracted from transgenic <italic>Arabidopsis</italic> expressing AtLYK5-HA in <italic>Atlyk5-2</italic> mutant plants. Plant tissues were harvested before (−) and 15 min after (+) treatment with 1 µM chitooctaose. Crude proteins from these tissues were boiled for 5 min before (−) or after (+) adding 50 mM DTT. Left panel and right panel of the immunoblot detected with anti-HA antibody are from the same gel.</p><p><bold>DOI:</bold> <ext-link ext-link-type="doi" xlink:href="10.7554/eLife.03766.020">http://dx.doi.org/10.7554/eLife.03766.020</ext-link></p></caption><graphic xlink:href="elife03766f007"/></fig><fig id="fig7s1" position="float" specific-use="child-fig"><object-id pub-id-type="doi">10.7554/eLife.03766.021</object-id><label>Figure 7—figure supplement 1.</label><caption><title>A possible working model of chitin receptor in Arabidopsis.</title><p>Before chitin treatment, AtLYK5 is present as a homodimer. After chitin elicitation, AtCERK1 associates with AtLYK5 to form a possible tetremer to mediate chitin signaling, and AtCERK1 will be phosphorylated at the same time. In this model, AtLYK5 (or AtLYK4) serves as a chitin perception, while AtCERK1 is responsible for chitin signaling transduction due to lack of kinase activity of AtLYK5 (or AtLYK4).</p><p><bold>DOI:</bold> <ext-link ext-link-type="doi" xlink:href="10.7554/eLife.03766.021">http://dx.doi.org/10.7554/eLife.03766.021</ext-link></p></caption><graphic xlink:href="elife03766fs012"/></fig></fig-group></p></sec></sec><sec id="s3" sec-type="discussion"><title>Discussion</title><p>The current model for AtCERK1 function indicates that this protein directly binds long chain chitooligosaccharides (dp ≥ 6), leading to homodimerization, kinase activation and downstream induction of MTI (<xref ref-type="bibr" rid="bib4">Bohm et al., 2014</xref>; <xref ref-type="bibr" rid="bib22">Kadota et al., 2014</xref>; <xref ref-type="bibr" rid="bib32">Liu et al., 2012b</xref>). The problem with this model is that it does not account for the relatively low binding affinity of AtCERK1 for chitin and the fact that mutations (AtCERK1<sup>A138H</sup>) predicted to disrupt chitin binding did not block AtCERK1 autophosphorylation (<xref ref-type="bibr" rid="bib32">Liu et al., 2012b</xref>). These discrepancies can now be explained by the interaction of AtCERK1 with AtLYK5, which binds chitin with a significantly higher affinity than AtCERK1. Indeed, AtLYK5 is required for AtCERK1 dimerization and also kinase activation. The data suggest that AtLYK5 exists in the cell, in the absence of chitin, as a homodimer. Chitin binds to AtLYK5 leading to its association with AtCERK1, dimerization and kinase activation. In this way, chitin signaling is transduced downstream through AtCERK1 kinase activity.</p><p>Our model, together with the studies from rice, suggests that AtCERK1 is not the primary chitin receptor. In rice, one long-chain chitooligosaccharide is sandwiched between two OsCEBiP monomers. Chitin treatment induces the association of OsCEBiP with OsCERK1, which activates the OsCERK1 intracellular kinase domain (<xref ref-type="bibr" rid="bib17">Hayafune et al., 2014</xref>; <xref ref-type="bibr" rid="bib49">Shimizu et al., 2010</xref>). However, in <italic>Arabidopsis</italic>, the three CEBiP-like proteins are not required for chitin-triggered innate immunity (<xref ref-type="bibr" rid="bib50">Shinya et al., 2012</xref>; <xref ref-type="bibr" rid="bib58">Wan et al., 2012</xref>). Instead, AtLYK5 appears to play a similar role as CEBiP as a chitin-binding receptor to mediate AtCERK1 activation through ligand-induced association. These two systems are very similar since both OsCEBiP and AtLYK5 lack the intracellular kinase function. OsCEBiP has no intracellular kinase domain, while AtLYK5 contains an intracellular kinase domain that lacks activity. However, the AtLYK5 intracellular kinase domain does appear to have biological function, likely by mediating protein–protein interactions. It is likely that the chitin receptor complex functions as a heterotetramer in both rice (<xref ref-type="bibr" rid="bib17">Hayafune et al., 2014</xref>) and <italic>Arabidopsis</italic> (<xref ref-type="fig" rid="fig7s1">Figure 7—figure supplement 1</xref>), although this needs to be confirmed. Such an oligomer complex could explain why in vitro receptor binding affinities (∼1 µM) do not correlate well with the measured responses of plants to chitin elicitation at nM concentrations (<xref ref-type="bibr" rid="bib65">Zhang et al., 2002</xref>). An oligomeric AtCERK1 receptor complex is also consistent with the finding that AtLYM1 and AtLYM3 (<xref ref-type="bibr" rid="bib63">Willmann et al., 2011</xref>) are necessary for PGN-induced MTI. All these studies suggest that the primary function of AtCERK1/OsCERK1 is not chitin binding per se, but to serve as a receptor scaffold for interaction with chitin binding co-receptors and, most importantly, to provide intracellular kinase activity.</p><p>Based on ITC data, AtLYK5 has similar chitooctaose binding affinity to that of wheat germ agglutinin (WGA) while, under the same conditions, AtCERK1 showed extremely low chitooctaose binding activity. Previously published data, also using ITC, measured the chitopentaose binding affinity of WGA in the low µM range, while the binding affinity (K<sub>d</sub>) to shorter chitin oligomers (GlcNAc)<sub>2–4</sub> was significantly lower (i.e., mM level; <xref ref-type="bibr" rid="bib2">Asensio, et al., 2000</xref>). ITC is one of the best methods to study protein–protein interactions or protein-ligand association. Since ITC detects protein–protein or protein-ligand interaction directly which is label-free, the binding affinity value might be slightly different from other methods. For example, in the case of WGA, ITC values (K<sub>d</sub>) for binding to chitobiose and chitotriose were 1.6 mM and 117 µM, respectively, (<xref ref-type="bibr" rid="bib2">Asensio, et al., 2000</xref>), while similar measurements using surface plasmon resonance (SPR) gave Kd values of 165 µM and 45 µM, respectively (<xref ref-type="bibr" rid="bib30">Lienenmann et al., 2009</xref>). Published reports for the chitin binding affinity for AtCERK1 also vary widely. For example, (<xref ref-type="bibr" rid="bib19">Iizasa et al., 2010</xref>) measured the affinity of AtCERK1 for chitin on a solid surface (commercial chitin magnetic beads) and reported a value (K<sub>d</sub>) of 82 nM. It is difficult to reconcile this number with other values obtained by ITC. One possible explanation is that the use of a solid surface promoted oligomerization of AtCERK1 resulting in an enhancement of binding affinity. In contrast, using ITC, the binding affinity (K<sub>d</sub>) of AtCERK1 for chitotetrose, chitopentaose, and chitooctaose was measured as 159 µM, 66 µM, and 45 µM, respectively (<xref ref-type="bibr" rid="bib32">Liu et al., 2012b</xref>). However, these studies were performed with significantly higher protein and ligand concentration (i.e., 0.1 mM AtCERK1 protein vs 4 mM chitotetraose or chitopentaose, and 2.4 mM chitooctaose) than used in our study. Again, such high protein concentrations could have promoted oligomerization of the AtCERK1 protein, which would affect the binding affinities.</p><p><italic>Arabidopsis</italic> has five LYK genes. We can now assign biological function to four of these proteins. AtLYK3 appears to be involved in recognizing short chain (dp = 4–5) lipo-chitooligosaccarides and chitooligosaccarides (<xref ref-type="bibr" rid="bib28">Liang et al., 2013</xref>). However, this recognition leads to a suppression of MTI. The role of AtLYK2 remains unknown but it should be noted that this gene shows very low expression in all tissues examined (<xref ref-type="bibr" rid="bib29">Liang et al, 2014</xref>). AtCERK1/AtLYK1, AtLYK4 and AtLYK5 all appear to mediate the plant response to chitin elicitation leading to MTI. Previously, we reported that the Ler ecotype <italic>Atlyk5-1</italic> mutant was not defective in chitin-induced MTI. However, our current data show that this mutant likely represents a weak mutant allele, perhaps due to the 3′ position of the transposon insertion. The Ler ecotype is also not ideal for studying chitin signaling since it shows a generally weaker response compared to Col-0. In contrast, the Col-0 ecotype <italic>Atlyk5-2</italic> mutant showed a reduced response to chitin treatment in all assays tested, including pathogen response. The phenotype of the <italic>Atlyk5-2</italic> mutant was reversed by genetic complementation with the wild-type AtLYK5 gene.</p><p>Chitin-induced MTI requires long chain chitin oligomers (dp ≥ 6) (<xref ref-type="bibr" rid="bib38">Miya et al., 2007</xref>; <xref ref-type="bibr" rid="bib59">Wan et al., 2008</xref>, <xref ref-type="bibr" rid="bib58">2012</xref>). The functions of AtLYK4 and AtLYK5 are partially redundant in that single mutants retain residual responses to chitin, while <italic>Atlyk4/Atlyk5-2</italic> double mutant plants show a complete lack of response to chitin, similar to the <italic>Atcerk1</italic> mutants. However, AtLYK5 appears to have the predominant role in chitin elicitation, as judged by the relative strength of the <italic>Atlyk4</italic> and <italic>Atlyk5-2</italic> mutant phenotypes. There are biochemical differences in the function of AtLYK4 and AtLYK5; for example, AtLYK4 interacts with AtCERK1 independently of the presence of chitin, while AtLYK5-AtCERK1 interaction is chitin dependent. The biological significance of these differences and the functional redundancy of AtLYK4 and AtLYK5 are currently unclear. One possibility is that AtLYK4 also functions as a chitin binding receptor to mediate the plant chitin repsonse.</p><p>Receptor homodimerization or oligomerization and subsequent phosphorylation are common mechanisms for ligand-mediate receptor activation. <italic>Arabidopsis</italic> examples include AtBRI1 homodimerization and heterodimerization with AtBAK1 (<xref ref-type="bibr" rid="bib26">Li et al., 2002</xref>; <xref ref-type="bibr" rid="bib41">Nam and Li, 2002</xref>; <xref ref-type="bibr" rid="bib48">Santiago, et al., 2013</xref>; <xref ref-type="bibr" rid="bib54">Sun, et al., 2013a</xref>; <xref ref-type="bibr" rid="bib60">Wang et al., 2005</xref>). AtFLS2 appears to exist in the cell as a homodimer before and after ligand perception and then associates with AtBAK1 upon flagellin treatment (<xref ref-type="bibr" rid="bib1">Albert, et al., 2013</xref>; <xref ref-type="bibr" rid="bib9">Chinchilla et al., 2007</xref>; <xref ref-type="bibr" rid="bib18">Heese et al., 2007</xref>; <xref ref-type="bibr" rid="bib53">Sun et al., 2012</xref>; <xref ref-type="bibr" rid="bib55">Sun, et al., 2013b</xref>). The suggested mechanism is that ligand perception triggers autophosphorylation between the homodimer or trans-autophosphorylation between/among hetero-interacting proteins to initiate cellular signaling. It appears that all LysM receptors may function as a protein complex. For example, in leguminous plants, the LysM domain, Nod factor receptors (e.g., <italic>Lotus japonicas</italic> Nod factor receptor 1 and 5; LjNFR1 and LjNFR5) function as a heterodimer to mediate high affinity binding to the lipo-chitooligosaccharide Nod factor (<xref ref-type="bibr" rid="bib6">Broghammer et al., 2012</xref>; <xref ref-type="bibr" rid="bib15">Gust et al., 2012</xref>; <xref ref-type="bibr" rid="bib35">Madsen et al., 2011</xref>; <xref ref-type="bibr" rid="bib45">Radutoiu et al., 2003</xref>). It should be emphasized that this model for Nod factor binding is very similar to that of the <italic>Arabidopsis</italic> chitin receptor. In both cases, one LysM RLK (CERK1/NFR1) has an active intracellular kinase domain but interacts with a second LysM RLK (LYK5/NFR5) that lacks intracellular kinase activity. This similarity underlines the now well recognized evolutionary link between chitin, Nod factor and mycorrhizal (Myc) factor recognition (<xref ref-type="bibr" rid="bib29">Liang et al., 2014</xref>).</p></sec><sec id="s4" sec-type="materials|methods"><title>Materials and methods</title><sec id="s4-1"><title>Plant material and treatment</title><p><italic>Arabidopsis</italic> mutant plants <italic>Atcerk1</italic> (GABI-KAT 096F09), <italic>Atlyk2</italic> (SAIL_318C08), At<italic>lyk3</italic> (SALK_140374), <italic>Atlyk4</italic> (CS850683), <italic>Atlyk5-2</italic> (SALK_131911C), and wild-type Col-0 plants were used in this study. Typically, 4-week-old <italic>Arabidopsis</italic> plants grown in a condition of 16 hr light/8 hr dark cycle at 22–23°C were used for diverse treatments. For chitin treatment, usually 1 µM chitooctaose (Sigma, St Louis, MO), unless otherwise mentioned, was used to treat plant tissues. Homozygous <italic>Atlyk5-2</italic> mutant and <italic>Atlyk4/Atlyk5-2</italic> double mutants plants were genotyped using primers listed in <xref ref-type="supplementary-material" rid="SD1-data">Supplemental file 1</xref>.</p></sec><sec id="s4-2"><title>Gene cloning and plasmid construction</title><p>All primers used for gene cloning are listed in <xref ref-type="supplementary-material" rid="SD1-data">Supplemental file 1</xref>. The full-length cDNAs of <italic>AtLYK2, AtLYK3, AtLYK4</italic>, and <italic>AtLYK5</italic> were amplified using the template made by <xref ref-type="bibr" rid="bib58">Wan et al. (2012)</xref> and cloned into pDONR-Zeo plasmid by BP cloning. The resultant plasmid was then used for LR cloning with destination plasmids pUC-GW14 and pUC-GW17 (<xref ref-type="bibr" rid="bib8">Cao et al., 2013</xref>). The resultant plasmids were used for protein expression in <italic>Arabidopsis</italic> protoplasts.</p><p>Two genomic DNA fragments, containing the 1.5 kb promoter of <italic>AtLYK4</italic> and <italic>AtLYK4</italic> coding region up to the stop codon and the 1.8 kb promoter of <italic>AtLYK5</italic> and <italic>AtLYK5</italic> coding region up to the stop codon, and cDNA of <italic>AtLYK5</italic>, were individually amplified with <italic>pfu</italic> Ultra II HF (Agilent Technologes, Santa Clara, CA) and cloned into the pDONR-Zeo vector using BP clonase (Invitrogen, Carlsbad, CA). The resulting plasmids were then recombined into the destination binary vector pGWB13 or pGWB5 (<xref ref-type="bibr" rid="bib40">Nakagawa et al., 2007</xref>) for <italic>Arabidopsis</italic> transformation or transient expression in <italic>N. benthamiana</italic>.</p><p>Kinase domains of AtLYK5 (309–664 aa) and AtCERK1 (255–617 aa) were amplified and inserted into pGEX 5X-1 between <italic>Eco</italic>R I and X<italic>ho</italic> I and between <italic>Eco</italic>R I and <italic>Sal</italic> I, separately, and transformed into BL21 (DE3) for recombinant protein expression.</p></sec><sec id="s4-3"><title><italic>Arabidopsis</italic> protoplast preparation and transformation</title><p><italic>Arabidopsis</italic> protoplasts were prepared from 4-week-old plants according to the protocol described by <xref ref-type="bibr" rid="bib64">Yoo et al. (2007)</xref>. For protein expression, protoplasts (200 µl, about 2 × 10<sup>5</sup> cells) were transfected with 20 µg plasmids. For co-immunoprecipitation assays, protoplasts (1 ml; ∼10<sup>6</sup> cells) were transfected with 100 µg plasmid. After incubation in a growth chamber at 23°C overnight (14–16 hr), the transfected protoplasts were treated with chitooctaose for the times shown in the figure legends and frozen in liquid nitrogen and stored in −80°C for further use.</p></sec><sec id="s4-4"><title>Co-immunoprecipitation assay</title><p>Samples from either protoplasts or plant tissues were lysed in a buffer containing 50 mM Tris (PH 7.6), 150 mM NaCl, 0.5% Triton X-100 and 1 × protease inhibitor (Sigma, MO). The resulting extract was centrifuged at 14,000 rpm for 15 min at 4°C. Either anti-Myc (Covance, Princeton, New Jersey) or anti-AtCERK1 antibody was used for CoIP experiments according the method described by <xref ref-type="bibr" rid="bib8">Cao et al. (2013)</xref>. Anti-AtCERK1 antibody was made based on the peptide N′-CNFQNEDLVSLMSGR-C′ located at c-terminal of AtCERK1 by GenScript Company (Piscataway, NJ).</p></sec><sec id="s4-5"><title>Chitin-induced CERK1 phosphorylation</title><p>1 µM chitooctaose or H<sub>2</sub>O was hand-infiltrated into leaves of different plants. At the time points shown in the figures, leaves were harvested and frozen in liquid nitrogen and ground using a Bead Ruptor Homogenizer (Omni, Kennesaw, GA). Samples were placed on ice for 30 min during the lysis. After centrifuging at 13,000 rpm at 4°C for 15 min, the supernatants were boiled for 5 min in 1 × SDS loading buffer. The phosphorylated AtCERK1 was separated on 7% SDS-PAGE gel at low voltage (60–80 V) for 4 hr or until the protein ladder with 70 kDa reached the bottom of the gel. For dephophorylation assay, antarctic phosphatase (New England Biolabs, Ipswich, MA) was used for treatment for 15 min at 37°C. AtCERK1 was detected with anti-AtCERK1 antibody.</p></sec><sec id="s4-6"><title>ROS production, MAPK phosphorylation, and pathogen assay</title><p>ROS production and MAPK phosphorylation assays were performed as described by <xref ref-type="bibr" rid="bib28">Liang et al. (2013)</xref>. The disease assay with <italic>A. brassicicola</italic> was conducted as described by <xref ref-type="bibr" rid="bib59">Wan et al. (2008)</xref>. 1 µM chitooctaose or H<sub>2</sub>O (control) was infiltrated into leaves from 4-week-old plants 24 hr before bacterial infiltration. The bacterial pathogen assay was carried out according to the method described by <xref ref-type="bibr" rid="bib8">Cao et al. (2013)</xref>.</p></sec><sec id="s4-7"><title>Calcium influx assay</title><p>Aequorin transgenic seeds were kindly provided by Dr Marc R Knight (University of Oxford). The <italic>Atlyk5-2</italic> mutant was crossed with Col-0 aequorin to make an <italic>Atlyk5-2</italic> aequorin line. Calcium influx assays were done using the same method described by <xref ref-type="bibr" rid="bib28">Liang et al. (2013)</xref>.</p></sec><sec id="s4-8"><title>Purification of GST-fusion protein and in vitro kinase assay</title><p>Purification of AtCERK1 and AtLYK5 intracellular domains fused with N-terminal GST tag and in vitro kinase assay were performed as described by <xref ref-type="bibr" rid="bib8">Cao et al. (2013)</xref>. Briefly, cultures of <italic>E. coli</italic> strains harboring plasmid were supplemented with 0.1 mM isopropyl b-D-thiogalactopyranoside (IPTG) at OD<sub>600</sub> 0.8 at 18°C for 12 hr. The cells were lysed in a buffer containing 1 × PBS (MP Biomedicals, France) supplemented with 1 mM EDTA, 0.1% Triton X-100, 1 mg/ml lysozyme and placed on ice for 30 min with slow shaking before sonication. After centrifuge at 4°C for 30 min, the supernatant was applied to a column containing glutathione Sepharose 4B (GE Healthcare, Milwaukee, WI) for protein purification. The column was washed five-times with 1 × PBS buffer. Recombinant proteins were eluted with 10 mM reduced glutathione. Proteins were dialyzed with a buffer containing 50 mM Tris (PH 7.6), 50 mM KCl, and 10% glycerol. For in vitro kinase assay, proteins were incubated in the buffer [50 mM Tris (PH 7.6), 50 mM KCl, 10 mM MnCl<sub>2</sub>, 10 mM MgCl<sub>2</sub>, 10 mM ATP, and 10 mCi γ-[<sup>32</sup>P]-ATP at room temperature for 30 min. Autoradiography was performed using a phosphor screen and a phosphorimager.</p></sec><sec id="s4-9"><title>Quantitative reverse transcript PCR (qRT-PCR)</title><p>Total RNA was extracted from 10-day-old seedlings using an RNase easy kit (Invitrogen, Grand Island, NY) according to the manufacturer's instructions. qRT-PCR was carried out as previously described by <xref ref-type="bibr" rid="bib55a">Tanaka et al. (2011)</xref>. The primers used are listed in <xref ref-type="supplementary-material" rid="SD1-data">Supplemental file 1</xref>.</p></sec><sec id="s4-10"><title><italic>Arabidopsis</italic> transformation assay</title><p>All the binary vectors were electroporated into <italic>Agrobacterium tumefaciens GV3101</italic> (pMP90) and transformed by the floral dip method (<xref ref-type="bibr" rid="bib11">Clough and Bent, 1998</xref>) into <italic>Atlyk5-2</italic> mutant plants. Transgenic plants were selected on half strength MS with 25 mg/l hygromycin after seed surface sterilization described by <xref ref-type="bibr" rid="bib11">Clough and Bent (1998)</xref>.</p></sec><sec id="s4-11"><title>Expression of AtLYK5-GFP in <italic>N. benthamiana</italic></title><p><italic>AtLYK5</italic> cDNA in pDONR-Zeo vector was recombined into binary vector pGWB5 using LR reaction. The resultant plasmid was electroporated into agrobacterial strain GV3101 for transiently expression in <italic>N. benthamiana</italic> according the method described by <xref ref-type="bibr" rid="bib58">Wan et al. (2012)</xref>. 2 days after infiltration, the infiltrated leaf was used to monitor fluorescence signal using confocal microscope.</p></sec><sec id="s4-12"><title>Purification of AtCERK1 and AtLYK5 ectodomains</title><p>The ectodomain of AtLYK5 (27–278 aa) was amplified and inserted into pMCSG73 using the ligation-independent procedure (PMID: 18988021). A thrombin cleavage site (LVPRGS) was inserted right before the His tag using site-directed mutagenesis PCR. Cultures of <italic>E. coli</italic> BL21, expressing the appropriate plasmid, were supplemented with 0.1 mM IPTG at OD<sub>600</sub> 0.8 at 18°C for 24 hr. Recombinant protein was purified with Talon metal affinity resin and eluted with 300 mM imidazole. Eluted protein was then incubated with thrombin at 4°C overnight and subsequently dialyzed with (50 mM Tris (PH 8.0) 150 mM NaCl). The resultant protein was purified over Strep-Tactin resin. The ectodomain of AtCERK1 (24–231 aa) was amplified and inserted into pMAL-c2G vector at the <italic>Bam</italic>H I and <italic>Sal</italic> I sites. After expression as described above, the recombinant protein was purified over amylose affinity resin according to the manufacturer's protocol (New England Biolabs, Ipswich, MA).</p></sec><sec id="s4-13"><title>Isothermal titration calorimetry</title><p>All protein samples including the ectodomains of AtLYK5 and AtCERK1, and wheat germ agglutinin (Sigma, St Louis, MO) were dialyzed against a buffer containing 10 mM HEPES, pH 7.5, 100 mM NaCl. Chitooctaose used for ITC was purchased from Sigma. 20 µM AtLYK5 or AtCERK1 purified protein or 10 µM wheat germ agglutinin (Sigma, St Louis, MO) was titrated separately against either 400 µM chitooctaose or 200 µM chitooctaose at 25°C. As a control, 10 µM AtLYK5 was titrated against 200 µM chitotetraose. Buffer lacking protein was used as control and titrated against 200 µM chitooctaose. The heat from each experiment was measured by MicroCal VP-ITC.</p></sec><sec id="s4-14"><title>Modeling and Docking</title><p>Homology modeling of the LysM domain of AtLYK5 was performed in the Modeller 9.12 (<xref ref-type="bibr" rid="bib36">Marti-Renom et al., 2000</xref>) using the crystallized structure of ECP6 was used as the template (PDB code 4B8V). The query sequence and template structure alignment was first performed using the Modeller Align module, and then manually inspected to ensure the best alignment for generating a pool of 2000 models. The best model was selected and analyzed based on Modeller's probability density function (Discrete Optimized Protein Energy score) and the Ramachandran plot (<xref ref-type="bibr" rid="bib24">Laskowski et al., 1993</xref>), and subsequently refined using the Loop refine module of Modeller.</p><p>In order to perform docking and calculate a binding affinity, the LysM model and the chitooctaose ligand (NCBI identifier 24978517) were prepared using the MGLTools-1.5.6 software (<xref ref-type="bibr" rid="bib39">Morris et al., 2009</xref>) to satisfy docking requirements such as addition of hydrogen atoms, calculation of partial charge using the AMBER force field (<xref ref-type="bibr" rid="bib11a">Cornell et al., 1995</xref>), selection of flexible bonds for the ligand and residues, and adjustment of docking position and grid space (parameters not shown). The putative binding site of the LysM domain model of AtLYK5 was inferred from the template structure. The docking experiment was then performed with the AutoDockVina software (<xref ref-type="bibr" rid="bib56">Trott and Olson, 2010</xref>), and the docking model with the lowest binding energy (expressed in kcal per mol) was selected and visualized in the Chimera software (<xref ref-type="bibr" rid="bib43">Pettersen et al., 2004</xref>). A detailed interaction map between the ligand and surrounding residues was generated by the LigPlus software (<xref ref-type="bibr" rid="bib57">Wallace et al., 1995</xref>).</p><p>To calculate the binding affinity of ECP6 to chitooctaose as a positive control, only the crystal model of ECP6 was retrieved for the docking task. The docking experiment with the chitooctaose ligand was performed with the AutoDock Vina software as mentioned above. The docking model with the lowest binding energy was selected and visualized.</p></sec></sec></body><back><ack id="ack"><title>Acknowledgements</title><p>We thank Dr Michael Henzl at the University of Missouri for the assistance using ITC and critical comments on this manuscript. We thank Mia Brown and Dr Jason Cooley for their assistance in obtaining CD spectra of AtLYK5 and AtCERK1 protein. We also thank ABRC for providing T-DNA insertion lines.</p></ack><sec sec-type="additional-information"><title>Additional information</title><fn-group content-type="competing-interest"><title>Competing interests</title><fn fn-type="conflict" id="conf1"><p>The authors declare that no competing interests exist.</p></fn></fn-group><fn-group content-type="author-contribution"><title>Author contributions</title><fn fn-type="con" id="con1"><p>YC, Conception and design, Acquisition of data, Analysis and interpretation of data, Drafting or revising the article</p></fn><fn fn-type="con" id="con2"><p>YL, Acquisition of data, Analysis and interpretation of data, Drafting or revising the article</p></fn><fn fn-type="con" id="con3"><p>KT, Acquisition of data, Analysis and interpretation of data</p></fn><fn fn-type="con" id="con4"><p>CTN, Acquisition of data, Analysis and interpretation of data</p></fn><fn fn-type="con" id="con5"><p>RPJ, Acquisition of data, Drafting or revising the article</p></fn><fn fn-type="con" id="con6"><p>AJ, Acquisition of data, Drafting or revising the article</p></fn><fn fn-type="con" id="con7"><p>GS, Conception and design, Analysis and interpretation of data, Drafting or revising the article</p></fn></fn-group></sec><sec sec-type="supplementary-material"><title>Additional files</title><supplementary-material id="SD1-data"><object-id pub-id-type="doi">10.7554/eLife.03766.022</object-id><label>Supplementary file 1.</label><caption><p>Primer sequences used in this study.</p><p><bold>DOI:</bold> <ext-link ext-link-type="doi" xlink:href="10.7554/eLife.03766.022">http://dx.doi.org/10.7554/eLife.03766.022</ext-link></p></caption><media mime-subtype="pdf" mimetype="application" xlink:href="elife03766s001.pdf"/></supplementary-material><sec sec-type="datasets"><title>Major dataset</title><p>The following previously published dataset was used:</p><p><related-object content-type="existing-dataset" source-id="http://www.pdb.org/pdb/explore/explore.do?structureId=4B8V" source-id-type="uri" id="dataro1"><collab collab-type="author">Sanchez-Vallet A</collab>, <collab collab-type="author">Saleem-Batcha R</collab>, <collab collab-type="author">Kombrink A</collab>, <collab collab-type="author">Hansen G</collab>, <collab collab-type="author">Valkenburg DJ</collab>, <collab collab-type="author">Thomma BPHJ</collab>, <collab collab-type="author">Mesters JR</collab>, <year>2013</year><x>, </x><source>Cladosporium fulvum LysM effector Ecp6 in complex with a beta-1,4- linked N-acetyl-D-glucosamine tetramer</source><x>, </x><ext-link ext-link-type="uri" xlink:href="http://www.pdb.org/pdb/explore/explore.do?structureId=4B8V">http://www.pdb.org/pdb/explore/explore.do?structureId=4B8V</ext-link><x>, </x><comment>Publicly available at RCSB Protein Data Bank.</comment></related-object></p></sec></sec><ref-list><title>References</title><ref id="bib1"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Albert</surname><given-names>M</given-names></name><name><surname>Jehle</surname><given-names>AK</given-names></name><name><surname>Fürst</surname><given-names>U</given-names></name><name><surname>Chinchilla</surname><given-names>D</given-names></name><name><surname>Boller</surname><given-names>T</given-names></name><name><surname>Felix</surname><given-names>G</given-names></name></person-group><year>2013</year><article-title>A two-hybrid-receptor assay demonstrates heteromer formation as switch-on for plant immune receptors</article-title><source>Plant Physiology</source><volume>163</volume><fpage>1504</fpage><lpage>1509</lpage><pub-id pub-id-type="doi">10.1104/pp.113.227736</pub-id></element-citation></ref><ref id="bib2"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Asensio</surname><given-names>JL</given-names></name><name><surname>Cañada</surname><given-names>FJ</given-names></name><name><surname>Siebert</surname><given-names>HC</given-names></name><name><surname>Laynez</surname><given-names>J</given-names></name><name><surname>Poveda</surname><given-names>A</given-names></name><name><surname>Nieto</surname><given-names>PM</given-names></name><name><surname>Soedjanaamadja</surname><given-names>UM</given-names></name><name><surname>Gabius</surname><given-names>HJ</given-names></name><name><surname>Jiménez-Barbero</surname><given-names>J</given-names></name></person-group><year>2000</year><article-title>Structural basis for chitin recognition by defense proteins: GlcNAc residues are bound in a multivalent fashion by extended binding sites in hevein domains</article-title><source>Chemistry &amp; Biology</source><volume>7</volume><fpage>529</fpage><lpage>543</lpage><pub-id pub-id-type="doi">10.1016/S1074-5521(00)00136-8</pub-id></element-citation></ref><ref id="bib3"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Bent</surname><given-names>AF</given-names></name><name><surname>Mackey</surname><given-names>D</given-names></name></person-group><year>2007</year><article-title>Elicitors, effectors, and R genes: the new paradigm and a lifetime supply of questions</article-title><source>Annual Review of Phytopathology</source><volume>45</volume><fpage>399</fpage><lpage>436</lpage><pub-id pub-id-type="doi">10.1146/annurev.phyto.45.062806.094427</pub-id></element-citation></ref><ref id="bib4"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Bohm</surname><given-names>H</given-names></name><name><surname>Albert</surname><given-names>I</given-names></name><name><surname>Fan</surname><given-names>L</given-names></name><name><surname>Reinhard</surname><given-names>A</given-names></name><name><surname>Nurnberger</surname><given-names>T</given-names></name></person-group><year>2014</year><article-title>Immune receptor complexes at the plant cell surface</article-title><source>Current Opinion in Plant Biology</source><volume>20</volume><fpage>47</fpage><lpage>54</lpage><pub-id pub-id-type="doi">10.1016/j.pbi.2014.04.007</pub-id></element-citation></ref><ref id="bib5"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Boller</surname><given-names>T</given-names></name><name><surname>Felix</surname><given-names>G</given-names></name></person-group><year>2009</year><article-title>A renaissance of elicitors: perception of microbe-associated molecular patterns and danger signals by pattern-recognition receptors</article-title><source>Annual Review of Plant Biology</source><volume>60</volume><fpage>379</fpage><lpage>406</lpage><pub-id pub-id-type="doi">10.1146/annurev.arplant.57.032905.105346</pub-id></element-citation></ref><ref id="bib6"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Broghammer</surname><given-names>A</given-names></name><name><surname>Krusell</surname><given-names>L</given-names></name><name><surname>Blaise</surname><given-names>M</given-names></name><name><surname>Sauer</surname><given-names>J</given-names></name><name><surname>Sullivan</surname><given-names>JT</given-names></name><name><surname>Maolanon</surname><given-names>N</given-names></name><name><surname>Vinther</surname><given-names>M</given-names></name><name><surname>Lorentzen</surname><given-names>A</given-names></name><name><surname>Madsen</surname><given-names>EB</given-names></name><name><surname>Jensen</surname><given-names>KJ</given-names></name><name><surname>Roepstorff</surname><given-names>P</given-names></name><name><surname>Thirup</surname><given-names>S</given-names></name><name><surname>Ronson</surname><given-names>CW</given-names></name><name><surname>Thygesen</surname><given-names>MB</given-names></name><name><surname>Stougaard</surname><given-names>J</given-names></name></person-group><year>2012</year><article-title>Legume receptors perceive the rhizobial lipochitin oligosaccharide signal molecules by direct binding</article-title><source>Proceedings of the National Academy of Sciences of USA</source><volume>109</volume><fpage>13859</fpage><lpage>13864</lpage><pub-id pub-id-type="doi">10.1073/pnas.1205171109</pub-id></element-citation></ref><ref id="bib8"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Cao</surname><given-names>Y</given-names></name><name><surname>Aceti</surname><given-names>DJ</given-names></name><name><surname>Sabat</surname><given-names>G</given-names></name><name><surname>Song</surname><given-names>J</given-names></name><name><surname>Makino</surname><given-names>S</given-names></name><name><surname>Fox</surname><given-names>BG</given-names></name><name><surname>Bent</surname><given-names>AF</given-names></name></person-group><year>2013</year><article-title>Mutations in FLS2 Ser-938 dissect signaling activation in FLS2-mediated <italic>Arabidopsis</italic> immunity</article-title><source>PLOS Pathogens</source><volume>9</volume><fpage>e1003313</fpage><pub-id pub-id-type="doi">10.1371/journal.ppat.1003313</pub-id></element-citation></ref><ref id="bib9"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Chinchilla</surname><given-names>D</given-names></name><name><surname>Zipfel</surname><given-names>C</given-names></name><name><surname>Robatzek</surname><given-names>S</given-names></name><name><surname>Kemmerling</surname><given-names>B</given-names></name><name><surname>Nurnberger</surname><given-names>T</given-names></name><name><surname>Jones</surname><given-names>JD</given-names></name><name><surname>Felix</surname><given-names>G</given-names></name><name><surname>Boller</surname><given-names>T</given-names></name></person-group><year>2007</year><article-title>A flagellin-induced complex of the receptor FLS2 and BAK1 initiates plant defence</article-title><source>Nature</source><volume>448</volume><fpage>497</fpage><lpage>500</lpage><pub-id pub-id-type="doi">10.1038/nature05999</pub-id></element-citation></ref><ref id="bib10"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Choi</surname><given-names>J</given-names></name><name><surname>Tanaka</surname><given-names>K</given-names></name><name><surname>Cao</surname><given-names>Y</given-names></name><name><surname>Qi</surname><given-names>Y</given-names></name><name><surname>Qiu</surname><given-names>J</given-names></name><name><surname>Liang</surname><given-names>Y</given-names></name><name><surname>Lee</surname><given-names>SY</given-names></name><name><surname>Stacey</surname><given-names>G</given-names></name></person-group><year>2014</year><article-title>Identification of a plant receptor for extracellular ATP</article-title><source>Science</source><volume>343</volume><fpage>290</fpage><lpage>294</lpage><pub-id pub-id-type="doi">10.1126/science.343.6168.290</pub-id></element-citation></ref><ref id="bib11"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Clough</surname><given-names>SJ</given-names></name><name><surname>Bent</surname><given-names>AF</given-names></name></person-group><year>1998</year><article-title>Floral dip: a simplified method for Agrobacterium-mediated transformation of <italic>Arabidopsis thaliana</italic></article-title><source>The Plant Journal</source><volume>16</volume><fpage>735</fpage><lpage>743</lpage><pub-id pub-id-type="doi">10.1046/j.1365-313x.1998.00343.x</pub-id></element-citation></ref><ref id="bib11a"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Cornell</surname><given-names>WD</given-names></name><name><surname>Cieplak</surname><given-names>P</given-names></name><name><surname>Bayly</surname><given-names>CI</given-names></name><name><surname>Gould</surname><given-names>IR</given-names></name><name><surname>Merz</surname><given-names>KM</given-names></name><name><surname>Ferguson</surname><given-names>DM</given-names></name><name><surname>Spellman</surname><given-names>DC</given-names></name><name><surname>Fox</surname><given-names>T</given-names></name><name><surname>Caldwell</surname><given-names>JW</given-names></name><name><surname>Kollman</surname><given-names>PA</given-names></name></person-group><year>1995</year><article-title>A second generation force field for the simulation of proteins, nucleic acids, and organic molecules</article-title><source>Journal of the American Chemical Society</source><volume>117</volume><fpage>5179</fpage><lpage>5197</lpage><pub-id pub-id-type="doi">10.1021/ja00124a002</pub-id></element-citation></ref><ref id="bib12"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Faulkner</surname><given-names>C</given-names></name><name><surname>Petutschnig</surname><given-names>E</given-names></name><name><surname>Benitez-Alfonso</surname><given-names>Y</given-names></name><name><surname>Beck</surname><given-names>M</given-names></name><name><surname>Robatzek</surname><given-names>S</given-names></name><name><surname>Lipka</surname><given-names>V</given-names></name><name><surname>Maule</surname><given-names>AJ</given-names></name></person-group><year>2013</year><article-title>LYM2-dependent chitin perception limits molecular flux via plasmodesmata</article-title><source>Proceedings of the National Academy of Sciences of USA</source><volume>110</volume><fpage>9166</fpage><lpage>9170</lpage><pub-id pub-id-type="doi">10.1073/pnas.1203458110</pub-id></element-citation></ref><ref id="bib13"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Gomez-Gomez</surname><given-names>L</given-names></name><name><surname>Boller</surname><given-names>T</given-names></name></person-group><year>2002</year><article-title>Flagellin perception: a paradigm for innate immunity</article-title><source>Trends in Plant Science</source><volume>7</volume><fpage>251</fpage><lpage>256</lpage><pub-id pub-id-type="doi">10.1016/S1360-1385(02)02261-6</pub-id></element-citation></ref><ref id="bib14"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Gomez-Gomez</surname><given-names>L</given-names></name><name><surname>Boller</surname><given-names>T</given-names></name></person-group><year>2000</year><article-title>FLS2: an LRR receptor-like kinase involved in the perception of the bacterial elicitor flagellin in <italic>Arabidopsis</italic></article-title><source>Molecular Cell</source><volume>5</volume><fpage>1003</fpage><lpage>1011</lpage><pub-id pub-id-type="doi">10.1016/S1097-2765(00)80265-8</pub-id></element-citation></ref><ref id="bib15"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Gust</surname><given-names>AA</given-names></name><name><surname>Willmann</surname><given-names>R</given-names></name><name><surname>Desaki</surname><given-names>Y</given-names></name><name><surname>Grabherr</surname><given-names>HM</given-names></name><name><surname>Nurnberger</surname><given-names>T</given-names></name></person-group><year>2012</year><article-title>Plant LysM proteins: modules mediating symbiosis and immunity</article-title><source>Trends in Plant Science</source><volume>17</volume><fpage>495</fpage><lpage>502</lpage><pub-id pub-id-type="doi">10.1016/j.tplants.2012.04.003</pub-id></element-citation></ref><ref id="bib16"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Hanks</surname><given-names>SK</given-names></name><name><surname>Quinn</surname><given-names>AM</given-names></name><name><surname>Hunter</surname><given-names>T</given-names></name></person-group><year>1988</year><article-title>The protein kinase family: conserved features and deduced phylogeny of the catalytic domains</article-title><source>Science</source><volume>241</volume><fpage>42</fpage><lpage>52</lpage><pub-id pub-id-type="doi">10.1126/science.3291115</pub-id></element-citation></ref><ref id="bib17"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Hayafune</surname><given-names>M</given-names></name><name><surname>Berisio</surname><given-names>R</given-names></name><name><surname>Marchetti</surname><given-names>R</given-names></name><name><surname>Silipo</surname><given-names>A</given-names></name><name><surname>Kayama</surname><given-names>M</given-names></name><name><surname>Desaki</surname><given-names>Y</given-names></name><name><surname>Arima</surname><given-names>S</given-names></name><name><surname>Squeglia</surname><given-names>F</given-names></name><name><surname>Ruggiero</surname><given-names>A</given-names></name><name><surname>Tokuyasu</surname><given-names>K</given-names></name><name><surname>Molinaro</surname><given-names>A</given-names></name><name><surname>Kaku</surname><given-names>H</given-names></name><name><surname>Shibuya</surname><given-names>N</given-names></name></person-group><year>2014</year><article-title>Chitin-induced activation of immune signaling by the rice receptor CEBiP relies on a unique sandwich-type dimerization</article-title><source>Proceedings of the National Academy of Sciences of USA</source><volume>111</volume><fpage>E404</fpage><lpage>E413</lpage><pub-id pub-id-type="doi">10.1073/pnas.1312099111</pub-id></element-citation></ref><ref id="bib18"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Heese</surname><given-names>A</given-names></name><name><surname>Hann</surname><given-names>DR</given-names></name><name><surname>Gimenez-Ibanez</surname><given-names>S</given-names></name><name><surname>Jones</surname><given-names>AM</given-names></name><name><surname>He</surname><given-names>K</given-names></name><name><surname>Li</surname><given-names>J</given-names></name><name><surname>Schroeder</surname><given-names>JI</given-names></name><name><surname>Peck</surname><given-names>SC</given-names></name><name><surname>Rathjen</surname><given-names>JP</given-names></name></person-group><year>2007</year><article-title>The receptor-like kinase SERK3/BAK1 is a central regulator of innate immunity in plants</article-title><source>Proceedings of the National Academy of Sciences of USA</source><volume>104</volume><fpage>12217</fpage><lpage>12222</lpage><pub-id pub-id-type="doi">10.1073/pnas.0705306104</pub-id></element-citation></ref><ref id="bib19"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Iizasa</surname><given-names>E</given-names></name><name><surname>Mitsutomi</surname><given-names>M</given-names></name><name><surname>Nagano</surname><given-names>Y</given-names></name></person-group><year>2010</year><article-title>Direct binding of a plant LysM receptor-like kinase, LysM RLK1/CERK1, to chitin in vitro</article-title><source>The Journal of Biological Chemistry</source><volume>285</volume><fpage>2996</fpage><lpage>3004</lpage><pub-id pub-id-type="doi">10.1074/jbc.M109.027540</pub-id></element-citation></ref><ref id="bib20"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Jiang</surname><given-names>G</given-names></name><name><surname>Hunter</surname><given-names>T</given-names></name></person-group><year>1999</year><article-title>Receptor signaling: when dimerization is not enough</article-title><source>Current Biology</source><volume>9</volume><fpage>R568</fpage><lpage>R571</lpage><pub-id pub-id-type="doi">10.1016/S0960-9822(99)80357-1</pub-id></element-citation></ref><ref id="bib21"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Jones</surname><given-names>JD</given-names></name><name><surname>Dangl</surname><given-names>JL</given-names></name></person-group><year>2006</year><article-title>The plant immune system</article-title><source>Nature</source><volume>444</volume><fpage>323</fpage><lpage>329</lpage><pub-id pub-id-type="doi">10.1038/nature05286</pub-id></element-citation></ref><ref id="bib22"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Kadota</surname><given-names>Y</given-names></name><name><surname>Sklenar</surname><given-names>J</given-names></name><name><surname>Derbyshire</surname><given-names>P</given-names></name><name><surname>Stransfeld</surname><given-names>L</given-names></name><name><surname>Asai</surname><given-names>S</given-names></name><name><surname>Ntoukakis</surname><given-names>V</given-names></name><name><surname>Jones</surname><given-names>JD</given-names></name><name><surname>Shirasu</surname><given-names>K</given-names></name><name><surname>Menke</surname><given-names>F</given-names></name><name><surname>Jones</surname><given-names>A</given-names></name><name><surname>Zipfel</surname><given-names>C</given-names></name></person-group><year>2014</year><article-title>Direct regulation of the NADPH oxidase RBOHD by the PRR-associated kinase BIK1 during plant immunity</article-title><source>Molecular Cell</source><volume>54</volume><fpage>43</fpage><lpage>55</lpage><pub-id pub-id-type="doi">10.1016/j.molcel.2014.02.021</pub-id></element-citation></ref><ref id="bib23"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Kaku</surname><given-names>H</given-names></name><name><surname>Nishizawa</surname><given-names>Y</given-names></name><name><surname>Ishii-Minami</surname><given-names>N</given-names></name><name><surname>Akimoto-Tomiyama</surname><given-names>C</given-names></name><name><surname>Dohmae</surname><given-names>N</given-names></name><name><surname>Takio</surname><given-names>K</given-names></name><name><surname>Minami</surname><given-names>E</given-names></name><name><surname>Shibuya</surname><given-names>N</given-names></name></person-group><year>2006</year><article-title>Plant cells recognize chitin fragments for defense signaling through a plasma membrane receptor</article-title><source>Proceedings of the National Academy of Sciences of USA</source><volume>103</volume><fpage>11086</fpage><lpage>11091</lpage><pub-id pub-id-type="doi">10.1073/pnas.0508882103</pub-id></element-citation></ref><ref id="bib24"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Laskowski</surname><given-names>RA</given-names></name><name><surname>MacArthur</surname><given-names>MW</given-names></name><name><surname>Moss</surname><given-names>DS</given-names></name><name><surname>Thornton</surname><given-names>JM</given-names></name></person-group><year>1993</year><article-title>PROCHECK: a program to check the stereochemical quality of protein structures</article-title><source>Journal of Applied Crystallography</source><volume>26</volume><fpage>283</fpage><lpage>291</lpage><pub-id pub-id-type="doi">10.1107/S0021889892009944</pub-id></element-citation></ref><ref id="bib25"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Li</surname><given-names>J</given-names></name><name><surname>Chory</surname><given-names>J</given-names></name></person-group><year>1997</year><article-title>A putative leucine-rich repeat receptor kinase involved in brassinosteroid signal transduction</article-title><source>Cell</source><volume>90</volume><fpage>929</fpage><lpage>938</lpage><pub-id pub-id-type="doi">10.1016/S0092-8674(00)80357-8</pub-id></element-citation></ref><ref id="bib26"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Li</surname><given-names>J</given-names></name><name><surname>Wen</surname><given-names>J</given-names></name><name><surname>Lease</surname><given-names>KA</given-names></name><name><surname>Doke</surname><given-names>JT</given-names></name><name><surname>Tax</surname><given-names>FE</given-names></name><name><surname>Walker</surname><given-names>JC</given-names></name></person-group><year>2002</year><article-title>BAK1, an <italic>Arabidopsis</italic> LRR receptor-like protein kinase, interacts with BRI1 and modulates brassinosteroid signaling</article-title><source>Cell</source><volume>110</volume><fpage>213</fpage><lpage>222</lpage><pub-id pub-id-type="doi">10.1016/S0092-8674(02)00812-7</pub-id></element-citation></ref><ref id="bib27"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Li</surname><given-names>L</given-names></name><name><surname>Li</surname><given-names>M</given-names></name><name><surname>Yu</surname><given-names>L</given-names></name><name><surname>Zhou</surname><given-names>Z</given-names></name><name><surname>Liang</surname><given-names>X</given-names></name><name><surname>Liu</surname><given-names>Z</given-names></name><name><surname>Cai</surname><given-names>G</given-names></name><name><surname>Gao</surname><given-names>L</given-names></name><name><surname>Zhang</surname><given-names>X</given-names></name><name><surname>Wang</surname><given-names>Y</given-names></name><name><surname>Chen</surname><given-names>S</given-names></name><name><surname>Zhou</surname><given-names>JM</given-names></name></person-group><year>2014</year><article-title>The FLS2-associated kinase BIK1 directly phosphorylates the NADPH oxidase RbohD to control plant immunity</article-title><source>Cell Host &amp; Microbe</source><volume>15</volume><fpage>329</fpage><lpage>338</lpage><pub-id pub-id-type="doi">10.1016/j.chom.2014.02.009</pub-id></element-citation></ref><ref id="bib28"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Liang</surname><given-names>Y</given-names></name><name><surname>Cao</surname><given-names>Y</given-names></name><name><surname>Tanaka</surname><given-names>K</given-names></name><name><surname>Thibivilliers</surname><given-names>S</given-names></name><name><surname>Wan</surname><given-names>J</given-names></name><name><surname>Choi</surname><given-names>J</given-names></name><name><surname>Kang</surname><given-names>C</given-names></name><name><surname>Qiu</surname><given-names>J</given-names></name><name><surname>Stacey</surname><given-names>G</given-names></name></person-group><year>2013</year><article-title>Nonlegumes respond to rhizobial Nod factors by suppressing the innate immune response</article-title><source>Science</source><volume>341</volume><fpage>1384</fpage><lpage>1387</lpage><pub-id pub-id-type="doi">10.1126/science.1242736</pub-id></element-citation></ref><ref id="bib29"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Liang</surname><given-names>Y</given-names></name><name><surname>Toth</surname><given-names>K</given-names></name><name><surname>Cao</surname><given-names>Y</given-names></name><name><surname>Tanaka</surname><given-names>K</given-names></name><name><surname>Espinoza</surname><given-names>C</given-names></name><name><surname>Stacey</surname><given-names>G</given-names></name></person-group><year>2014</year><article-title>Lipochitooligosaccharide recognition: an ancient story</article-title><source>The New Phytologist</source><volume>204</volume><fpage>289</fpage><lpage>296</lpage><pub-id pub-id-type="doi">10.1111/nph.12898</pub-id></element-citation></ref><ref id="bib30"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Lienemann</surname><given-names>M</given-names></name><name><surname>Paananen</surname><given-names>A</given-names></name><name><surname>Boer</surname><given-names>H</given-names></name><name><surname>de la Fuente</surname><given-names>JM</given-names></name><name><surname>García</surname><given-names>I</given-names></name><name><surname>Penadés</surname><given-names>S</given-names></name><name><surname>Koivula</surname><given-names>A</given-names></name></person-group><year>2009</year><article-title>Characterization of the wheat germ agglutinin binding to self-assembled monolayers of neoglycoconjugates by AFM and SPR</article-title><source>Glycobiology</source><volume>19</volume><fpage>633</fpage><lpage>643</lpage><pub-id pub-id-type="doi">10.1093/glycob/cwp030</pub-id></element-citation></ref><ref id="bib31"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Liu</surname><given-names>B</given-names></name><name><surname>Li</surname><given-names>JF</given-names></name><name><surname>Ao</surname><given-names>Y</given-names></name><name><surname>Qu</surname><given-names>J</given-names></name><name><surname>Li</surname><given-names>Z</given-names></name><name><surname>Su</surname><given-names>J</given-names></name><name><surname>Zhang</surname><given-names>Y</given-names></name><name><surname>Liu</surname><given-names>J</given-names></name><name><surname>Feng</surname><given-names>D</given-names></name><name><surname>Qi</surname><given-names>K</given-names></name><name><surname>He</surname><given-names>Y</given-names></name><name><surname>Wang</surname><given-names>J</given-names></name><name><surname>Wang</surname><given-names>HB</given-names></name></person-group><year>2012a</year><article-title>Lysin motif-containing proteins LYP4 and LYP6 play dual roles in peptidoglycan and chitin perception in rice innate immunity</article-title><source>The Plant Cell</source><volume>24</volume><fpage>3406</fpage><lpage>3419</lpage><pub-id pub-id-type="doi">10.1105/tpc.112.102475</pub-id></element-citation></ref><ref id="bib32"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Liu</surname><given-names>T</given-names></name><name><surname>Liu</surname><given-names>Z</given-names></name><name><surname>Song</surname><given-names>C</given-names></name><name><surname>Hu</surname><given-names>Y</given-names></name><name><surname>Han</surname><given-names>Z</given-names></name><name><surname>She</surname><given-names>J</given-names></name><name><surname>Fan</surname><given-names>F</given-names></name><name><surname>Wang</surname><given-names>J</given-names></name><name><surname>Jin</surname><given-names>C</given-names></name><name><surname>Chang</surname><given-names>J</given-names></name><name><surname>Zhou</surname><given-names>JM</given-names></name><name><surname>Chai</surname><given-names>J</given-names></name></person-group><year>2012b</year><article-title>Chitin-induced dimerization activates a plant immune receptor</article-title><source>Science</source><volume>336</volume><fpage>1160</fpage><lpage>1164</lpage><pub-id pub-id-type="doi">10.1126/science.1218867</pub-id></element-citation></ref><ref id="bib33"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Lu</surname><given-names>D</given-names></name><name><surname>Wu</surname><given-names>S</given-names></name><name><surname>Gao</surname><given-names>X</given-names></name><name><surname>Zhang</surname><given-names>Y</given-names></name><name><surname>Shan</surname><given-names>L</given-names></name><name><surname>He</surname><given-names>P</given-names></name></person-group><year>2010</year><article-title>A receptor-like cytoplasmic kinase, BIK1, associates with a flagellin receptor complex to initiate plant innate immunity</article-title><source>Proceedings of the National Academy of Sciences of USA</source><volume>107</volume><fpage>496</fpage><lpage>501</lpage><pub-id pub-id-type="doi">10.1073/pnas.0909705107</pub-id></element-citation></ref><ref id="bib34"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Macho</surname><given-names>AP</given-names></name><name><surname>Zipfel</surname><given-names>C</given-names></name></person-group><year>2014</year><article-title>Plant PRRs and the activation of innate immune signaling</article-title><source>Molecular Cell</source><volume>54</volume><fpage>263</fpage><lpage>272</lpage><pub-id pub-id-type="doi">10.1016/j.molcel.2014.03.028</pub-id></element-citation></ref><ref id="bib35"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Madsen</surname><given-names>EB</given-names></name><name><surname>Antolin-Llovera</surname><given-names>M</given-names></name><name><surname>Grossmann</surname><given-names>C</given-names></name><name><surname>Ye</surname><given-names>J</given-names></name><name><surname>Vieweg</surname><given-names>S</given-names></name><name><surname>Broghammer</surname><given-names>A</given-names></name><name><surname>Krusell</surname><given-names>L</given-names></name><name><surname>Radutoiu</surname><given-names>S</given-names></name><name><surname>Jensen</surname><given-names>ON</given-names></name><name><surname>Stougaard</surname><given-names>J</given-names></name><name><surname>Parniske</surname><given-names>M</given-names></name></person-group><year>2011</year><article-title>Autophosphorylation is essential for the in vivo function of the Lotus japonicus Nod factor receptor 1 and receptor-mediated signalling in cooperation with Nod factor receptor 5</article-title><source>The Plant Journal</source><volume>65</volume><fpage>404</fpage><lpage>417</lpage><pub-id pub-id-type="doi">10.1111/j.1365-313X.2010.04431.x</pub-id></element-citation></ref><ref id="bib36"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Marti-Renom</surname><given-names>MA</given-names></name><name><surname>Stuart</surname><given-names>AC</given-names></name><name><surname>Fiser</surname><given-names>A</given-names></name><name><surname>Sanchez</surname><given-names>R</given-names></name><name><surname>Melo</surname><given-names>F</given-names></name><name><surname>Sali</surname><given-names>A</given-names></name></person-group><year>2000</year><article-title>Comparative protein structure modeling of genes and genomes</article-title><source>Annual Review of Biophysics and Biomolecular Structure</source><volume>29</volume><fpage>291</fpage><lpage>325</lpage><pub-id pub-id-type="doi">10.1146/annurev.biophys.29.1.291</pub-id></element-citation></ref><ref id="bib37"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Mellado</surname><given-names>M</given-names></name><name><surname>Vila-Coro</surname><given-names>AJ</given-names></name><name><surname>Martinez</surname><given-names>C</given-names></name><name><surname>Rodriguez-Frade</surname><given-names>JM</given-names></name></person-group><year>2001</year><article-title>Receptor dimerization: a key step in chemokine signaling</article-title><source>Cellular and Molecular Biology</source><volume>47</volume><fpage>575</fpage><lpage>582</lpage></element-citation></ref><ref id="bib38"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Miya</surname><given-names>A</given-names></name><name><surname>Albert</surname><given-names>P</given-names></name><name><surname>Shinya</surname><given-names>T</given-names></name><name><surname>Desaki</surname><given-names>Y</given-names></name><name><surname>Ichimura</surname><given-names>K</given-names></name><name><surname>Shirasu</surname><given-names>K</given-names></name><name><surname>Narusaka</surname><given-names>Y</given-names></name><name><surname>Kawakami</surname><given-names>N</given-names></name><name><surname>Kaku</surname><given-names>H</given-names></name><name><surname>Shibuya</surname><given-names>N</given-names></name></person-group><year>2007</year><article-title>CERK1, a LysM receptor kinase, is essential for chitin elicitor signaling in <italic>Arabidopsis</italic></article-title><source>Proceedings of the National Academy of Sciences of USA</source><volume>104</volume><fpage>19613</fpage><lpage>19618</lpage><pub-id pub-id-type="doi">10.1073/pnas.0705147104</pub-id></element-citation></ref><ref id="bib39"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Morris</surname><given-names>GM</given-names></name><name><surname>Huey</surname><given-names>R</given-names></name><name><surname>Lindstrom</surname><given-names>W</given-names></name><name><surname>Sanner</surname><given-names>MF</given-names></name><name><surname>Belew</surname><given-names>RK</given-names></name><name><surname>Goodsell</surname><given-names>DS</given-names></name><name><surname>Olson</surname><given-names>AJ</given-names></name></person-group><year>2009</year><article-title>AutoDock4 and AutoDockTools4: Automated docking with selective receptor flexibility</article-title><source>Journal of Computational Chemistry</source><volume>30</volume><fpage>2785</fpage><lpage>2791</lpage><pub-id pub-id-type="doi">10.1002/jcc.21256</pub-id></element-citation></ref><ref id="bib40"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Nakagawa</surname><given-names>T</given-names></name><name><surname>Kurose</surname><given-names>T</given-names></name><name><surname>Hino</surname><given-names>T</given-names></name><name><surname>Tanaka</surname><given-names>K</given-names></name><name><surname>Kawamukai</surname><given-names>M</given-names></name><name><surname>Niwa</surname><given-names>Y</given-names></name><name><surname>Toyooka</surname><given-names>K</given-names></name><name><surname>Matsuoka</surname><given-names>K</given-names></name><name><surname>Jinbo</surname><given-names>T</given-names></name><name><surname>Kimura</surname><given-names>T</given-names></name></person-group><year>2007</year><article-title>Development of series of gateway binary vectors, pGWBs, for realizing efficient construction of fusion genes for plant transformation</article-title><source>Journal of Bioscience and Bioengineering</source><volume>104</volume><fpage>34</fpage><lpage>41</lpage><pub-id pub-id-type="doi">10.1263/jbb.104.34</pub-id></element-citation></ref><ref id="bib41"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Nam</surname><given-names>KH</given-names></name><name><surname>Li</surname><given-names>JM</given-names></name></person-group><year>2002</year><article-title>BRI1/BAK1, a receptor kinase pair mediating brassinosteroid signaling</article-title><source>Cell</source><volume>110</volume><fpage>203</fpage><lpage>212</lpage><pub-id pub-id-type="doi">10.1016/S0092-8674(02)00814-0</pub-id></element-citation></ref><ref id="bib42"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Pang</surname><given-names>X</given-names></name><name><surname>Zhou</surname><given-names>HX</given-names></name></person-group><year>2013</year><article-title>Activation of signaling receptors: do ligands bind to receptor monomer, dimer, or both?</article-title><source>BMC Biophys</source><volume>6</volume><fpage>7</fpage><pub-id pub-id-type="doi">10.1186/2046-1682-6-7</pub-id></element-citation></ref><ref id="bib43"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Pettersen</surname><given-names>EF</given-names></name><name><surname>Goddard</surname><given-names>TD</given-names></name><name><surname>Huang</surname><given-names>CC</given-names></name><name><surname>Couch</surname><given-names>GS</given-names></name><name><surname>Greenblatt</surname><given-names>DM</given-names></name><name><surname>Meng</surname><given-names>EC</given-names></name><name><surname>Ferrin</surname><given-names>TE</given-names></name></person-group><year>2004</year><article-title>UCSF Chimera–a visualization system for exploratory research and analysis</article-title><source>Journal of Computational Chemistry</source><volume>25</volume><fpage>1605</fpage><lpage>1612</lpage><pub-id pub-id-type="doi">10.1002/jcc.20084</pub-id></element-citation></ref><ref id="bib44"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Petutschnig</surname><given-names>EK</given-names></name><name><surname>Jones</surname><given-names>AM</given-names></name><name><surname>Serazetdinova</surname><given-names>L</given-names></name><name><surname>Lipka</surname><given-names>U</given-names></name><name><surname>Lipka</surname><given-names>V</given-names></name></person-group><year>2010</year><article-title>The lysin motif receptor-like kinase (LysM-RLK) CERK1 is a major chitin-binding protein in <italic>Arabidopsis thaliana</italic> and subject to chitin-induced phosphorylation</article-title><source>The Journal of Biological Chemistry</source><volume>285</volume><fpage>28902</fpage><lpage>28911</lpage><pub-id pub-id-type="doi">10.1074/jbc.M110.116657</pub-id></element-citation></ref><ref id="bib45"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Radutoiu</surname><given-names>S</given-names></name><name><surname>Madsen</surname><given-names>LH</given-names></name><name><surname>Madsen</surname><given-names>EB</given-names></name><name><surname>Felle</surname><given-names>HH</given-names></name><name><surname>Umehara</surname><given-names>Y</given-names></name><name><surname>Gronlund</surname><given-names>M</given-names></name><name><surname>Sato</surname><given-names>S</given-names></name><name><surname>Nakamura</surname><given-names>Y</given-names></name><name><surname>Tabata</surname><given-names>S</given-names></name><name><surname>Sandal</surname><given-names>N</given-names></name><name><surname>Stougaard</surname><given-names>J</given-names></name></person-group><year>2003</year><article-title>Plant recognition of symbiotic bacteria requires two LysM receptor-like kinases</article-title><source>Nature</source><volume>425</volume><fpage>585</fpage><lpage>592</lpage><pub-id pub-id-type="doi">10.1038/nature02039</pub-id></element-citation></ref><ref id="bib46"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Roux</surname><given-names>M</given-names></name><name><surname>Schwessinger</surname><given-names>B</given-names></name><name><surname>Albrecht</surname><given-names>C</given-names></name><name><surname>Chinchilla</surname><given-names>D</given-names></name><name><surname>Jones</surname><given-names>A</given-names></name><name><surname>Holton</surname><given-names>N</given-names></name><name><surname>Malinovsky</surname><given-names>FG</given-names></name><name><surname>Tör</surname><given-names>M</given-names></name><name><surname>de Vries</surname><given-names>S</given-names></name><name><surname>Zipfel</surname><given-names>C</given-names></name></person-group><year>2011</year><article-title>The <italic>Arabidopsis</italic> leucine-rich repeat receptor-like kinases BAK1/SERK3 and BKK1/SERK4 are required for innate immunity to hemibiotrophic and biotrophic pathogens</article-title><source>The Plant Cell</source><volume>23</volume><fpage>2440</fpage><lpage>2455</lpage><pub-id pub-id-type="doi">10.1105/tpc.111.084301</pub-id></element-citation></ref><ref id="bib47"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Sanchez-Vallet</surname><given-names>A</given-names></name><name><surname>Saleem-Batcha</surname><given-names>R</given-names></name><name><surname>Kombrink</surname><given-names>A</given-names></name><name><surname>Hansen</surname><given-names>G</given-names></name><name><surname>Valkenburg</surname><given-names>DJ</given-names></name><name><surname>Thomma</surname><given-names>BP</given-names></name><name><surname>Mesters</surname><given-names>JR</given-names></name></person-group><year>2013</year><article-title>Fungal effector Ecp6 outcompetes host immune receptor for chitin binding through intrachain LysM dimerization</article-title><source>eLife</source><volume>2</volume><fpage>e00790</fpage><pub-id pub-id-type="doi">10.7554/eLife.00790</pub-id></element-citation></ref><ref id="bib48"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Santiago</surname><given-names>J</given-names></name><name><surname>Henzler</surname><given-names>C</given-names></name><name><surname>Hothorn</surname><given-names>M</given-names></name></person-group><year>2013</year><article-title>Molecular mechanism for plant steroid receptor activation by somatic embryogenesis co-receptor kinases</article-title><source>Science</source><volume>341</volume><fpage>889</fpage><lpage>802</lpage><pub-id pub-id-type="doi">10.1126/science.1242468</pub-id></element-citation></ref><ref id="bib49"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Shimizu</surname><given-names>T</given-names></name><name><surname>Nakano</surname><given-names>T</given-names></name><name><surname>Takamizawa</surname><given-names>D</given-names></name><name><surname>Desaki</surname><given-names>Y</given-names></name><name><surname>Ishii-Minami</surname><given-names>N</given-names></name><name><surname>Nishizawa</surname><given-names>Y</given-names></name><name><surname>Minami</surname><given-names>E</given-names></name><name><surname>Okada</surname><given-names>K</given-names></name><name><surname>Yamane</surname><given-names>H</given-names></name><name><surname>Kaku</surname><given-names>H</given-names></name><name><surname>Shibuya</surname><given-names>N</given-names></name></person-group><year>2010</year><article-title>Two LysM receptor molecules, CEBiP and OsCERK1, cooperatively regulate chitin elicitor signaling in rice</article-title><source>The Plant Journal</source><volume>64</volume><fpage>204</fpage><lpage>214</lpage><pub-id pub-id-type="doi">10.1111/j.1365-313X.2010.04324.x</pub-id></element-citation></ref><ref id="bib50"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Shinya</surname><given-names>T</given-names></name><name><surname>Motoyama</surname><given-names>N</given-names></name><name><surname>Ikeda</surname><given-names>A</given-names></name><name><surname>Wada</surname><given-names>M</given-names></name><name><surname>Kamiya</surname><given-names>K</given-names></name><name><surname>Hayafune</surname><given-names>M</given-names></name><name><surname>Kaku</surname><given-names>H</given-names></name><name><surname>Shibuya</surname><given-names>N</given-names></name></person-group><year>2012</year><article-title>Functional characterization of CEBiP and CERK1 homologs in <italic>Arabidopsis</italic> and rice reveals the presence of different chitin receptor systems in plants</article-title><source>Plant &amp; Cell Physiology</source><volume>53</volume><fpage>1696</fpage><lpage>1706</lpage><pub-id pub-id-type="doi">10.1093/pcp/pcs113</pub-id></element-citation></ref><ref id="bib51"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Shiu</surname><given-names>SH</given-names></name><name><surname>Bleecker</surname><given-names>AB</given-names></name></person-group><year>2001</year><article-title>Receptor-like kinases from <italic>Arabidopsis</italic> form a monophyletic gene family related to animal receptor kinases</article-title><source>Proceedings of the National Academy of Sciences of USA</source><volume>98</volume><fpage>10763</fpage><lpage>10768</lpage><pub-id pub-id-type="doi">10.1073/pnas.181141598</pub-id></element-citation></ref><ref id="bib52"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Stock</surname><given-names>J</given-names></name></person-group><year>1996</year><article-title>Receptor signaling: dimerization and beyond</article-title><source>Current Biology</source><volume>6</volume><fpage>825</fpage><lpage>827</lpage><pub-id pub-id-type="doi">10.1016/S0960-9822(02)00605-X</pub-id></element-citation></ref><ref id="bib53"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Sun</surname><given-names>W</given-names></name><name><surname>Cao</surname><given-names>Y</given-names></name><name><surname>Jansen Labby</surname><given-names>K</given-names></name><name><surname>Bittel</surname><given-names>P</given-names></name><name><surname>Boller</surname><given-names>T</given-names></name><name><surname>Bent</surname><given-names>AF</given-names></name></person-group><year>2012</year><article-title>Probing the <italic>Arabidopsis</italic> flagellin receptor: FLS2-FLS2 association and the contributions of specific domains to signaling function</article-title><source>The Plant Cell</source><volume>24</volume><fpage>1096</fpage><lpage>1113</lpage><pub-id pub-id-type="doi">10.1105/tpc.112.095919</pub-id></element-citation></ref><ref id="bib54"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Sun</surname><given-names>Y</given-names></name><name><surname>Han</surname><given-names>Z</given-names></name><name><surname>Tang</surname><given-names>J</given-names></name><name><surname>Hu</surname><given-names>Z</given-names></name><name><surname>Chai</surname><given-names>C</given-names></name><name><surname>Zhou</surname><given-names>B</given-names></name><name><surname>Chai</surname><given-names>J</given-names></name></person-group><year>2013a</year><article-title>Structure reveals that BAK1 as a co-receptor recognizes the BRI1-bound brassinolide</article-title><source>Cell Research</source><volume>23</volume><fpage>1326</fpage><lpage>1329</lpage><pub-id pub-id-type="doi">10.1038/cr.2013.131</pub-id></element-citation></ref><ref id="bib55"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Sun</surname><given-names>Y</given-names></name><name><surname>Li</surname><given-names>L</given-names></name><name><surname>Macho</surname><given-names>AP</given-names></name><name><surname>Han</surname><given-names>Z</given-names></name><name><surname>Hu</surname><given-names>Z</given-names></name><name><surname>Zipfel</surname><given-names>C</given-names></name><name><surname>Zhou</surname><given-names>JM</given-names></name><name><surname>Chai</surname><given-names>J</given-names></name></person-group><year>2013b</year><article-title>Structural basis for flg22-induced activation of the <italic>Arabidopsis</italic> FLS2-BAK1 immune complex</article-title><source>Science</source><volume>342</volume><fpage>624</fpage><lpage>628</lpage><pub-id pub-id-type="doi">10.1126/science.1243825</pub-id></element-citation></ref><ref id="bib55a"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Tanaka</surname><given-names>K</given-names></name><name><surname>Nguyen</surname><given-names>TC</given-names></name><name><surname>Libault</surname><given-names>M</given-names></name><name><surname>Cheng</surname><given-names>J</given-names></name><name><surname>Stacey</surname><given-names>G</given-names></name></person-group><year>2011</year><article-title>Enzymatic activity of the soybean ecto-apyrase GS52 is essential for stimulation of nodulation</article-title><source>Plant Physiol</source><volume>155</volume><fpage>1988</fpage><lpage>1998</lpage><pub-id pub-id-type="doi">10.1104/pp.110.170910</pub-id></element-citation></ref><ref id="bib56"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Trott</surname><given-names>O</given-names></name><name><surname>Olson</surname><given-names>AJ</given-names></name></person-group><year>2010</year><article-title>AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading</article-title><source>Journal of Computational Chemistry</source><volume>31</volume><fpage>455</fpage><lpage>461</lpage><pub-id pub-id-type="doi">10.1002/jcc.21334</pub-id></element-citation></ref><ref id="bib57"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Wallace</surname><given-names>AC</given-names></name><name><surname>Laskowski</surname><given-names>RA</given-names></name><name><surname>Thornton</surname><given-names>JM</given-names></name></person-group><year>1995</year><article-title>LIGPLOT: a program to generate schematic diagrams of protein-ligand interactions</article-title><source>Protein Engineering</source><volume>8</volume><fpage>127</fpage><lpage>134</lpage><pub-id pub-id-type="doi">10.1093/protein/8.2.127</pub-id></element-citation></ref><ref id="bib58"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Wan</surname><given-names>J</given-names></name><name><surname>Tanaka</surname><given-names>K</given-names></name><name><surname>Zhang</surname><given-names>XC</given-names></name><name><surname>Son</surname><given-names>GH</given-names></name><name><surname>Brechenmacher</surname><given-names>L</given-names></name><name><surname>Nguyen</surname><given-names>TH</given-names></name><name><surname>Stacey</surname><given-names>G</given-names></name></person-group><year>2012</year><article-title>LYK4, a lysin motif receptor-like kinase, is important for chitin signaling and plant innate immunity in <italic>Arabidopsis</italic></article-title><source>Plant Physiology</source><volume>160</volume><fpage>396</fpage><lpage>406</lpage><pub-id pub-id-type="doi">10.1104/pp.112.201699</pub-id></element-citation></ref><ref id="bib59"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Wan</surname><given-names>J</given-names></name><name><surname>Zhang</surname><given-names>XC</given-names></name><name><surname>Neece</surname><given-names>D</given-names></name><name><surname>Ramonell</surname><given-names>KM</given-names></name><name><surname>Clough</surname><given-names>S</given-names></name><name><surname>Kim</surname><given-names>SY</given-names></name><name><surname>Stacey</surname><given-names>MG</given-names></name><name><surname>Stacey</surname><given-names>G</given-names></name></person-group><year>2008</year><article-title>A LysM receptor-like kinase plays a critical role in chitin signaling and fungal resistance in <italic>Arabidopsis</italic></article-title><source>Plant Cell</source><volume>20</volume><fpage>471</fpage><lpage>481</lpage><pub-id pub-id-type="doi">10.1105/tpc.107.056754</pub-id></element-citation></ref><ref id="bib60"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Wang</surname><given-names>X</given-names></name><name><surname>Li</surname><given-names>X</given-names></name><name><surname>Meisenhelder</surname><given-names>J</given-names></name><name><surname>Hunter</surname><given-names>T</given-names></name><name><surname>Yoshida</surname><given-names>S</given-names></name><name><surname>Asami</surname><given-names>T</given-names></name><name><surname>Chory</surname><given-names>J</given-names></name></person-group><year>2005</year><article-title>Autoregulation and homodimerization are involved in the activation of the plant steroid receptor BRI1</article-title><source>Developmental Cell</source><volume>8</volume><fpage>855</fpage><lpage>865</lpage><pub-id pub-id-type="doi">10.1016/j.devcel.2005.05.001</pub-id></element-citation></ref><ref id="bib61"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Weiberg</surname><given-names>A</given-names></name><name><surname>Wang</surname><given-names>M</given-names></name><name><surname>Bellinger</surname><given-names>M</given-names></name><name><surname>Jin</surname><given-names>H</given-names></name></person-group><year>2014</year><article-title>Small RNAs: a new paradigm in plant-microbe interactions</article-title><source>Annual Review of Phytopathology</source><volume>52</volume><fpage>495</fpage><lpage>516</lpage><pub-id pub-id-type="doi">10.1146/annurev-phyto-102313-045933</pub-id></element-citation></ref><ref id="bib62"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Weiberg</surname><given-names>A</given-names></name><name><surname>Wang</surname><given-names>M</given-names></name><name><surname>Lin</surname><given-names>FM</given-names></name><name><surname>Zhao</surname><given-names>H</given-names></name><name><surname>Zhang</surname><given-names>Z</given-names></name><name><surname>Kaloshian</surname><given-names>I</given-names></name><name><surname>Huang</surname><given-names>HD</given-names></name><name><surname>Jin</surname><given-names>H</given-names></name></person-group><year>2013</year><article-title>Fungal small RNAs suppress plant immunity by hijacking host RNA interference pathways</article-title><source>Science</source><volume>342</volume><fpage>118</fpage><lpage>123</lpage><pub-id pub-id-type="doi">10.1126/science.1239705</pub-id></element-citation></ref><ref id="bib63"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Willmann</surname><given-names>R</given-names></name><name><surname>Lajunen</surname><given-names>HM</given-names></name><name><surname>Erbs</surname><given-names>G</given-names></name><name><surname>Newman</surname><given-names>MA</given-names></name><name><surname>Kolb</surname><given-names>D</given-names></name><name><surname>Tsuda</surname><given-names>K</given-names></name><name><surname>Katagiri</surname><given-names>F</given-names></name><name><surname>Fliegmann</surname><given-names>J</given-names></name><name><surname>Bono</surname><given-names>JJ</given-names></name><name><surname>Cullimore</surname><given-names>JV</given-names></name><name><surname>Jehle</surname><given-names>AK</given-names></name><name><surname>Götz</surname><given-names>F</given-names></name><name><surname>Kulik</surname><given-names>A</given-names></name><name><surname>Molinaro</surname><given-names>A</given-names></name><name><surname>Lipka</surname><given-names>V</given-names></name><name><surname>Gust</surname><given-names>AA</given-names></name><name><surname>Nürnberger</surname><given-names>T</given-names></name></person-group><year>2011</year><article-title><italic>Arabidopsis</italic> lysin-motif proteins LYM1 LYM3 CERK1 mediate bacterial peptidoglycan sensing and immunity to bacterial infection</article-title><source>Proceedings of the National Academy of Sciences of USA</source><volume>108</volume><fpage>19824</fpage><lpage>19829</lpage><pub-id pub-id-type="doi">10.1073/pnas.1112862108</pub-id></element-citation></ref><ref id="bib64"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Yoo</surname><given-names>SD</given-names></name><name><surname>Cho</surname><given-names>YH</given-names></name><name><surname>Sheen</surname><given-names>J</given-names></name></person-group><year>2007</year><article-title><italic>Arabidopsis</italic> mesophyll protoplasts: a versatile cell system for transient gene expression analysis</article-title><source>Nature Protocols</source><volume>2</volume><fpage>1565</fpage><lpage>1572</lpage><pub-id pub-id-type="doi">10.1038/nprot.2007.199</pub-id></element-citation></ref><ref id="bib65"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Zhang</surname><given-names>B</given-names></name><name><surname>Ramonell</surname><given-names>K</given-names></name><name><surname>Somerville</surname><given-names>S</given-names></name><name><surname>Stacey</surname><given-names>G</given-names></name></person-group><year>2002</year><article-title>Characterization of early, chitin-induced gene expression in <italic>Arabidopsis</italic></article-title><source>Molecular Plant-Microbe Interactions</source><volume>15</volume><fpage>963</fpage><lpage>970</lpage><pub-id pub-id-type="doi">10.1094/MPMI.2002.15.9.963</pub-id></element-citation></ref><ref id="bib66"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Zhang</surname><given-names>J</given-names></name><name><surname>Li</surname><given-names>W</given-names></name><name><surname>Xiang</surname><given-names>T</given-names></name><name><surname>Liu</surname><given-names>Z</given-names></name><name><surname>Laluk</surname><given-names>K</given-names></name><name><surname>Ding</surname><given-names>X</given-names></name><name><surname>Zou</surname><given-names>Y</given-names></name><name><surname>Gao</surname><given-names>M</given-names></name><name><surname>Zhang</surname><given-names>X</given-names></name><name><surname>Chen</surname><given-names>S</given-names></name><name><surname>Mengiste</surname><given-names>T</given-names></name><name><surname>Zhang</surname><given-names>Y</given-names></name><name><surname>Zhou</surname><given-names>JM</given-names></name></person-group><year>2010</year><article-title>Receptor-like cytoplasmic kinases integrate signaling from multiple plant immune receptors and are targeted by a <italic>Pseudomonas syringae</italic> effector</article-title><source>Cell Host &amp; Microbe</source><volume>7</volume><fpage>290</fpage><lpage>301</lpage><pub-id pub-id-type="doi">10.1016/j.chom.2010.03.007</pub-id></element-citation></ref><ref id="bib67"><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Zipfel</surname><given-names>C</given-names></name><name><surname>Kunze</surname><given-names>G</given-names></name><name><surname>Chinchilla</surname><given-names>D</given-names></name><name><surname>Caniard</surname><given-names>A</given-names></name><name><surname>Jones</surname><given-names>JD</given-names></name><name><surname>Boller</surname><given-names>T</given-names></name><name><surname>Felix</surname><given-names>G</given-names></name></person-group><year>2006</year><article-title>Perception of the bacterial PAMP EF-Tu by the receptor EFR restricts Agrobacterium-mediated transformation</article-title><source>Cell</source><volume>125</volume><fpage>749</fpage><lpage>760</lpage><pub-id pub-id-type="doi">10.1016/j.cell.2006.03.037</pub-id></element-citation></ref></ref-list></back><sub-article article-type="article-commentary" id="SA1"><front-stub><article-id pub-id-type="doi">10.7554/eLife.03766.023</article-id><title-group><article-title>Decision letter</article-title></title-group><contrib-group content-type="section"><contrib contrib-type="editor"><name><surname>Nürnberger</surname><given-names>Thorsten</given-names></name><role>Reviewing editor</role><aff><institution>Tübingen University</institution>, <country>Germany</country></aff></contrib></contrib-group></front-stub><body><boxed-text><p>eLife posts the editorial decision letter and author response on a selection of the published articles (subject to the approval of the authors). An edited version of the letter sent to the authors after peer review is shown, indicating the substantive concerns or comments; minor concerns are not usually shown. Reviewers have the opportunity to discuss the decision before the letter is sent (see <ext-link ext-link-type="uri" xlink:href="http://elifesciences.org/review-process">review process</ext-link>). Similarly, the author response typically shows only responses to the major concerns raised by the reviewers.</p></boxed-text><p>Thank you for sending your work entitled “Arabidopsis CERK1 is not the primary chitin receptor but acts as a co-receptor with LYK5 to induce plant innate immunity” for consideration at <italic>eLife.</italic> Your article has been favorably evaluated by Detlef Weigel (Senior editor) and 3 reviewers, one of whom, Thorsten Nürnberger, is a member of our Board of Reviewing Editors.</p><p>The Reviewing editor and the other reviewers discussed their comments before we reached this decision, and the Reviewing editor has assembled the following comments to help you prepare a revised submission.</p><p>All reviewers agree that your manuscript potentially makes a very valuable contribution to <italic>eLife.</italic> In particular, the roles of LYK5 and CERK1 as a genuine chitin receptor/co-receptor pair are exciting findings that could help clarify several issues about major differences between chitin perception systems in different plants. Prior to acceptance you need, however, to address the issues listed below: 1) A major criticism concerns the binding data obtained by ITC. While an affinity constant for WGA (for a positive control) is given, there is no comparable number for chitin affinities of AtCERK1 and AtLYK5. The only statement found is that AtLYK5 has a comparable Kd as WGA, and is 200-fold more sensitive to chitin than AtCERK1. It was unclear to us, however, how the numbers given in <xref ref-type="fig" rid="fig3">Figure 3</xref> or any information in the text support these statements. Here, it is absolutely mandatory to give Kd values and an easily understandable description of how these values were determined. In addition, it should be shown that chitin binding as determined by ITC is ligand-specific. Here, competition assays with elicitor-active and inactive chitin fragments should be provided. In addition, a comprehensive discussion of apparent discrepancies between published chitin binding constants for CERK1 (Liu, 2012 45 uM, <xref ref-type="bibr" rid="bib19">Iizasa, 2010</xref>, 82 nM) and those determined in this study should be provided. This is important as the authors claim that the binding affinity of LYK5 is substantially higher than that of CERK1 and thus makes this protein the genuine chitin receptor.</p><p>2) Evidence should be provided that CEERK1 and LYK5 both operate in the same cell types/tissues. This is important as it might rule out that both proteins are chitin receptors with different tissue or cell-type specificities.</p><p>3) <xref ref-type="fig" rid="fig1">Figure 1A</xref>: As previous papers have incorrectly overlooked LYK5 as required for chitin perception, we think this figure needs all of the lyk mutants and a water control. Also; statistics are not clear here or throughout the manuscript. It is not stated what comparison “*” is referred to. Please show the control as 100% and calculate the other samples relative to that. And please explain why you are using at this point wrky29 and wrky30 and not as previously wrky33 and wrky53?</p><p>4) <xref ref-type="fig" rid="fig3">Figure 3</xref>: The ITC for LYK4 should be done as well, to see if a weaker binding of LYK4 compared to LYK5/CERK1 correlates with the physiological data (ROS, WRKY activation). Overall LYK4 is poorly dealt with in the current manuscript.</p></body></sub-article><sub-article article-type="reply" id="SA2"><front-stub><article-id pub-id-type="doi">10.7554/eLife.03766.024</article-id><title-group><article-title>Author response</article-title></title-group></front-stub><body><p><italic>1) A major criticism concerns the binding data obtained by ITC. While an affinity constant for WGA (for a positive control) is given, there is no comparable number for chitin affinities of AtCERK1 and AtLYK5. The only statement found is that AtLYK5 has a comparable Kd as WGA, and is 200-fold more sensitive to chitin than AtCERK1. It was unclear to us, however, how the numbers given in</italic> <xref ref-type="fig" rid="fig3">Figure 3</xref> <italic>or any information in the text support these statements. Here, it is absolutely mandatory to give Kd values and an easily understandable description of how these values were determined. In addition, it should be shown that chitin binding as determined by ITC is ligand-specific. Here, competition assays with elicitor-active and inactive chitin fragments should be provided. In addition, a comprehensive discussion of apparent discrepancies between published chitin binding constants for CERK1 (</italic>Liu, 2012 <italic>45 uM,</italic> <xref ref-type="bibr" rid="bib19">Iizasa, 2010</xref><italic>, 82 nM) and those determined in this study should be provided. This is important as the authors claim that the binding affinity of LYK5 is substantially higher than that of CERK1 and thus makes this protein the genuine chitin receptor</italic>.</p><p>This is a great point. The Kd value for each protein is now provided in the revised manuscript.</p><p>Unfortunately, we could not conduct the competition experiment as you suggest. This is because the ITC method detects protein-ligand interaction based on the differential heat after binding of ligand. Hence, ITC cannot distinguish heat changes produced by LYK5-chitooctaose, or by LYK5- inactive chitin, such as chitotetraose. However, to address criticism, we did conduct direct binding studies of LYK5 with chitotetraose and found no binding (See <xref ref-type="fig" rid="fig3s1">Figure 3—figure supplement 1</xref>). Therefore, as would be expected of a receptor involved in chitin elicitation, LYK5 appears to prefer longer chitin oligomers.</p><p>We added a detailed discussion regarding the binding affinity of CERK1. Basically, we feel that the previous studies had technical flaws and, in both cases, binding was done under conditions that would be predicted to favor protein oligomerization which would give an artificially higher binding affinity. In the case of Liu et al this is due to the very high concentrations of protein (0.1 mM) and ligand (4mM or 2.4mM) used in their binding assays. In the case of Iizasa et al, oligomerization would have been favored due to the fact that binding was measured against a solid substrate (chitin beads). Of course, this is conjecture on our part but we believe this is a likely explanation for the apparent discrepancy in the results. Perhaps more importantly, in our case, since we used proteins purified at the same time and assays done under identical conditions, a direct comparison of AtCERK1 and AtLYK5 binding was possible.</p><p><italic>2) Evidence should be provided that CEERK1 and LYK5 both operate in the same cell types/tissues. This is important as it might rule out that both proteins are chitin receptors with different tissue or cell-type specificities</italic>.</p><p>Yes, we did real time quantitative RT-PCR using templates from different growth ages and different tissues, and found that CERK1, LYK4 and LYK5 shared a similar expression pattern in all samples tested. The only slight variation was that LYK5 had higher expression in root than CERK1 or LYK4 (See <xref ref-type="fig" rid="fig1">Figure 1H</xref> and Figure S1N). Our data is consistent with the expression pattern calculated by an online software AtGenExpress Visualization Tool (AVT): <ext-link ext-link-type="uri" xlink:href="http://jsp.weigelworld.org/expviz/expviz.jsp">http://jsp.weigelworld.org/expviz/expviz.jsp</ext-link>.</p><p>Also, work of another postdoc in the lab has shown that both LYK5 and CERK1 are localized to the plasma membrane, also consistent with their direct interaction.</p><p><italic>3)</italic> <xref ref-type="fig" rid="fig1">Figure 1A</xref><italic>: As previous papers have incorrectly overlooked LYK5 as required for chitin perception, we think this figure needs all of the lyk mutants and a water control. Also; statistics are not clear here or throughout the manuscript. It is not stated what comparison “*” is referred to. Please show the control as 100% and calculate the other samples relative to that. And please explain why you are using at this point wrky29 and wrky30 and not as previously wrky33 and wrky53</italic>?</p><p>We retested chitin-triggered ROS production using all five <italic>lyk</italic> mutant plants (see <xref ref-type="fig" rid="fig1s5">Figure 1—figure supplement 5</xref>). These results showed that only <italic>cerk1</italic>, <italic>lyk4</italic> and <italic>lyk5-2</italic> are involved in the chitin response. We also rewrote the section on the statistical analysis and hope that it is now clearer. As we have reported in past talks, we believe that <italic>lyk2</italic> is likely a pseudogene, or at least is not expressed under any conditions tested, while, as we published in Science, LYK3 appears to recognize Nod factor and short chain chitin oligomers. Hence, with this current paper and our past work, we have assigned a function to all of the Arabidopsis LYK proteins that are expressed.</p><p>We analyzed the expression of <italic>WRKY33</italic> and <italic>WRKY53</italic> in <italic>lyk5-2</italic> mutant plants. The data showed that the expression of these two genes was greatly reduced after chitin treatment compared with wild-type plants (<xref ref-type="fig" rid="fig1s4">Figure1—figure supplement 4</xref>).</p><p><italic>4)</italic> <xref ref-type="fig" rid="fig3">Figure 3</xref><italic>: The ITC for LYK4 should be done as well, to see if a weaker binding of LYK4 compared to LYK5/CERK1 correlates with the physiological data (ROS, WRKY activation). Overall LYK4 is poorly dealt with in the current manuscript</italic>.</p><p>Actually, It is a very interesting question. We are also very curious about the binding affinity of AtLYK4.</p><p>However, the problem is that expression and purification of the LysM protein is very difficult. Based on our own experience, this is due to an inability to express the proteins in sufficient quantity for such studies. We consider ourselves fortunate that we were able to get enough CERK1 and LYK5 proteins to do the studies described in the paper. Unfortunately, the same was not true of LYK4. Using the same conditions we used for CERK1/LYK4, we tried to express the LYK4 extracellular domain in <italic>E.coli</italic> but obtained poor expression. What protein that was produced was insoluble and efforts to solubilize and refold have, thus far, proven unsuccessful. Therefore, although we would like to address the reviewers and our own curiosity about LYK4, this is going to have to wait until we work out a condition to get sufficient protein for binding studies. Since our current paper focuses on LYK5, these experiments concerning LYK4 are not really pertinent to the story being described. The data support the model that LYK5 is the major chitin binding protein, while LYK4 plays a minor role. We certainly hope to overcome the technical problems with regard to LYK4 expression and, if successful, will likely publish this as a separate story with the main focus on LYK4.</p></body></sub-article></article>