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The genome of Arabidopsis thaliana encodes more than 600 receptor-like kinase (RLK) genes, by far the dominant class of receptors found in land plants. Although similar to the mammalian receptor tyrosine kinases, plant RLKs are serine/threonine kinases that represent a novel signaling innovation unique to plants and, consequently, an excellent opportunity to understand how extracellular signaling evolved and functions in plants as opposed to animals. RLKs are predicted to be major components of the signaling pathways that allow plants to respond to environmental and developmental conditions. However, breakthroughs in identifying these processes have been limited to only a handful of individual RLKs. Here, we used a Syngenta custom Arabidopsis GeneChip array to compile a detailed profile of the transcriptional activity of 604 receptor-like kinase genes after exposure to a cross-section of known signaling factors in plants, including abiotic stresses, biotic stresses, and hormones. In the 68 experiments comprising the study, we found that 582 of the 604 RLK genes displayed a two-fold or greater change in expression to at least one of 12 types of treatments, thereby providing a large body of experimental evidence for targeted functional screens of individual RLK genes. We investigated whether particular subfamilies of RLK genes are responsive to specific types of signals and found that each subfamily displayed broad ranges of expression, as opposed to being targeted towards particular signal classes. Finally, by analyzing the divergence of sequence and gene expression among the RLK subfamilies, we present evidence as to the functional basis for the expansion of the RLKs and how this expansion may have affected conservation and divergences in their function. Taken as a whole, our study represents a preliminary, working model of processes and interactions in which the members of the RLK gene family may be involved, where such information has remained elusive for so many of its members.
The emergence of multicellularity in eukaryotes represents a sophisticated achievement in evolutionary history. Although its exact origins remain obscure, multicellularity appears to have evolved independently in a variety of eukaryotic phyla, perhaps many times (Kaiser, 2001; Bonner, 1998; King, 2004). Despite these broad beginnings, a unifying requirement of multicellularity is the capacity for individual cells to sense environmental and developmental cues in order to coordinate their behavior with neighboring cells (Pires-daSilva and Sommer, 2003). Not surprisingly, the genomes of multicellular organisms encode a number of molecular mechanisms that confer such sensory capacity during environmental and developmental responses.
In particular, a number of classes of cell-surface receptors have evolved that service the extracellular signaling needs of multicellular organisms (Ben-Shlomo et al., 2003). These classes include seven-transmembrane receptors, such as the G-protein-coupled receptors (GPCRs); enzyme-linked receptors, such as the receptor tyrosine kinases (RTKs) and receptor serine/threonine kinases (RS/TKs); ion-channel-linked receptors; and two-component histidine kinase receptors. Of these classes, the ion-channel-linked receptors and two-component receptors appear in both prokaryotic and eukaryotic lineages, suggesting that these forms of signaling are of truly ancient origin (Koishi et al., 2004; Hoch, 2000; Stock et al., 2000).
However, a survey of eukaryotic-specific receptors found in plants reveals an interesting divergence from the animal kingdom in terms of receptor evolution. One surprising result from the analysis of the complete genome sequence of Arabidopsis thaliana is the apparent absence of receptor tyrosine kinases and the presence of only two putative GPCRs (Meyerowitz, 2002; Perfus-Barbeoch et al., 2004; Liu et al., 2007). Instead, the Arabidopsis genome contains an expansive set of receptor serine/threonine kinases, known as receptor-like kinases (RLKs), which are unique to the plant kingdom (Shiu and Bleecker, 2001a; Shiu et al., 2004). RLKs comprise a more than 600-member gene family in Arabidopsis, representing approximately 2% of the predicted protein coding genome. Like the animal RTKs and RS/TKs, the majority of Arabidopsis RLKs appear to consist of an intracellular kinase domain, a single-pass transmembrane helix, and an extracellular region containing signaling-related sequence motifs (Cock et al., 2002). However, phylogenetic analyses support their classification as a monophyletic group that evolved separately from animal receptor kinases (Shiu and Bleecker, 2001a).
Current experimental results from a variety of plant species indicate that genes encoding RLKs are involved in a range of environmental and developmental responses, including recognition of pathogens (Xa21, FLS2, EFR) (Song et al., 1995; Gomez-Gomez and Boller, 2000; Zipfel et al., 2006), symbionts (NORK, SYMRK, NFR1, NFR5) (Endre et al., 2002; Stracke et al., 2002; Madsen et al., 2003; Radutoiu et al., 2003), and self (SRK) (Stein et al., 1991; Kachroo et al., 2001); perception of the plant hormones brassinosteroid (BRI1, BAK1/AtSERK3, BRL1, BRL3) (Li and Chory, 1997; Wang et al., 2001; Kinoshita et al., 2005; Nam and Li, 2002; Li et al., 2002; Zhou et al., 2004; Cano-Delgado et al., 2004) and phytosulfokine (PSKR) (Matsubayashi et al., 2002), as well as abscisic acid responsiveness (RPK1) (Osakabe et al., 2005); cell proliferation (ER, ERL1, ERL2) (Torii et al., 1996; Shpak et al., 2004); cell fate (CR4, EXS/EMS1, SCM/SUB, SERK1, SERK2) (Becraft et al., 1996; Canales et al., 2002; Zhao et al., 2002; Kwak et al., 2005; Chevalier et al., 2005; Colcombet et al., 2005; Albrecht et al., 2005); cell expansion (WAK2, WAK4) (Lally et al., 2001; Wagner and Kohorn, 2001); meristem regulation (CLV1, BAM1-3, FON1, TD1) (Clark et al., 1997; DeYoung et al., 2006; Suzaki et al., 2004; Bommert et al., 2005); vascular development (PXY) (Fisher and Turner, 2007); and, root and nodule growth (HAR1, NARK, SUNN) (Nishimura et al., 2002; Searle et al., 2003; Schnabel et al., 2005).
Collectively, RLKs represent a novel signaling innovation in plants and, consequently, an excellent opportunity to understand how extracellular signaling evolved and functions in plants as opposed to animals. However, many basic questions regarding their evolution and function remain unresolved. For example, the sheer number of Arabidopsis RLKs and the breadth of motifs found in their extracellular domains suggest their involvement in a number of physiological processes. But, the nature and range of these processes have yet to be identified for all but a handful of the more than 600 Arabidopsis RLKs. Furthermore, phylogenetic analysis of the Arabidopsis RLKs supports their classification into 43 subfamilies, which correspond to the type and organization of motifs found in their extracellular domains. For this reason, it has been hypothesized that members of a given subfamily may respond to similar types of signals. But, this hypothesis has yet to be tested. Finally, the functional implications of the evolutionary expansion of RLKs in the Arabidopsis genome remain unclear. The large sizes of the RLK subfamilies may indicate functional redundancies among its members. On the other hand, this phenomenon may have allowed for functional divergences to have evolved among its members, thereby allowing for an expanded functional range of the RLKs as a whole.
To address these issues, we performed a systematic, large-scale analysis of the transcriptional response of the Arabidopsis RLK gene family to a host of known environmental and developmental stimuli in plants. Here, we report on the conditions under which RLK gene expression is modulated, both on an individual gene level and on the subfamily level. We also profile similarities and divergences in gene expression among the individual RLK genes, as well as within the framework of the RLK subfamilies. Finally, we present a comparative analysis of the associations between gene expression patterns and sequence distances and divergence rates in an attempt to understand the evolutionary basis for the expansion and retention of the RLK superfamily.
As sessile, autotrophic organisms, plants are particularly reliant on environmental factors to guide their physiological and developmental programs. A number of studies have embraced the use of expression profiling to elucidate the molecular components involved in the signaling pathways that coordinate such programs (Nemhauser et al., 2006; Denby and Gehring, 2005; Takahashi et al., 2004; Hazen et al., 2003; Rabbani et al., 2003; Chen et al., 2002; Cheong et al., 2002; Kreps et al., 2002). Additionally, studies of several of the Arabidopsis RLKs have revealed gene expression changes, as well as the emergence of RLK mutant phenotypes, under specific stress elicitors and hormones (Shiu and Bleecker, 2001b; Osakabe et al., 2005; Verica et al., 2003; Sivaguru et al., 2003; He et al., 1998). However, a comprehensive profile of the transcriptional response of Arabidopsis receptor-like kinase genes to known signaling factors had yet to be produced.
For this reason, we addressed whether, and to what extent, Arabidopsis RLK genes are responsive to a host of well studied environmental and developmental signaling factors in plants. Specifically, we used the Syngenta custom Arabidopsis GeneChip array (sySYNG002a, Affymetrix, Santa Clara, California, USA) to assay changes in RLK transcript levels after exposure to 12 categories of treatments, representing three basic, though complex, classes of plant physiological responses: abiotic stress, biotic stress, and hormonal/chemical. Collectively, 102 arrays representing 68 experiments were analyzed. The 12 specific treatments included cold (4°C), gravity (vertical rotation), high light (1500μmolm−2s−1), osmotic stress (200mM mannitol), salt (100mM NaCl), bacterial pathogens (Pseudomonas syringae strains DC3000 and ES4326), fungal pathogens (Botrytis cinerea, Erysiphe, Peronospora parasitica, Phytophthora porri), viral pathogens (beet curly top hybrigeminivirus, cauliflower mosaic virus, cucumber mosaic virus, oilseed rape mosaic virus, tobacco rattle virus, turnip mosaic virus, turnip vein-clearing virus), abscisic acid (1μM, 10μM), glucose (0.3%, 3.0%, 6.0%), auxin (0.1μM), and jasmonic acid (45 and 50μM). Given that stress, disease, and hormones have both immediate and long-term effects on gene expression, many of the treatments in this analysis represent data generated from more than one time point, in an attempt to capture a larger portion of the range of responses (Nemhauser et al., 2006; Kreps et al., 2002). These treatments include cold, high light, osmotic stress, salt, auxin, jasmonic acid, and most of the pathogens. However, data from some treatments (glucose, abscisic acid) represent changes seen at single time points under differing concentrations. Supplemental Table 1 contains a description of the individual experiments.
Based on our analysis, we identified responses equal to or greater than a two-fold difference in expression from 582 of the 604 Arabidopsis RLK genes in at least one of the 12 treatments in our study (Figure 1A). Interestingly, of the 12 treatment groups, the bacterial, fungal, and viral pathogens elicited the largest proportion of differentially expressed RLK genes (60%), compared to the abiotic stresses (18%) and hormone/chemical treatments (22%) (Figure 1B). The hormone and chemical treatments also had a relatively large number of responses, in comparison with the abiotic stresses. In some treatment categories, individual RLK genes registered an up-regulated response in one experiment and a down-regulated response in another. In the case of time-course-based experiments, this result would suggest the temporal nature of the transcriptional activity of the given RLK gene. However, in experiments in which the nature of the treatment differed, such as with the pathogens, the diverse transcriptional response would indicate a disparate role in signaling activities related to the different treatments comprising that category. As a result of these dynamic responses, the total of number of respondents for a given treatment in some cases was smaller than the summation of up-regulated and down-regulated genes observed for that category of treatment.
Though it is tempting to speculate that the large number of pathogenesis-related responses may be due to an evolutionary process, the response proportions may be reflective of the proportion of experiments performed per treatment class: 61% biotic stresses, 14% abiotic stresses, and 25% hormone/chemical. To better understand this distribution, we also calculated the number of differentially expressed RLK genes per treatment, scaled by the number of experiments used in each treatment and the number of genes analyzed (Figure 1C and 1D). Based on this analysis, relatively large numbers of differentially expressed RLK genes were registered for the osmotic stress, abscisic acid, bacterial pathogen, cold, and glucose treatments. Table 1 lists the RLK genes with the top increased and decreased expression levels per treatment.
The results of the absolute and scaled analyses indicate that a large number of RLK genes are responsive to known signaling factors, and that the responses cover a range of plant physiological programs, including the response to abiotic and biotic stresses, as well as hormone and chemical-related processes. Given that mutant phenotypes in Arabidopsis often present themselves only under the appropriate, functionally relevant screening conditions, the specific treatments and RLK gene responses identified here serve as a resource for the targeted screening of individual RLK genetic mutants. The full list of differentially expressed RLK genes for all 68 experiments can be viewed in Supplemental Table 2. For a detailed description of the data analysis, see Methods.
Previously, it had been discovered that individual RLKs might be responsive to more than one signaling factor and thereby participate in multiple signaling pathways (Johnson and Ingram, 2005; Morris and Walker, 2003; Montoya et al., 2002). To investigate this phenomenon, we calculated the number of treatments to which individual RLK genes were differentially expressed, as well as the overlap in responses among the different conditions. First, we looked at the distribution of the number of overall responses registered by individual RLK genes across the 12 treatments (Figure 2A). Of the 604 RLK genes, 22 (4%) displayed no response to any of the experimental conditions tested, and 43 (7%) displayed an increase or decrease in expression to exactly one condition. The remaining number of respondents displayed an increase or decrease in expression to more than one condition. We also found a large number of genes that showed an increase or decrease in expression to more than one condition when looking at up-regulated responses and down-regulated responses separately (Figure 2B).
These results support the idea that single RLK genes may be involved in several physiological processes or in a common downstream process initiated by more than one condition. To identify those conditions under which individual RLK genes display multiple responses, we performed a Venn diagram-based analysis. Specifically, we looked for relationships among sets of responding RLK genes under conditions that are known to produce related physiological responses in plants (Figure 3A). In looking at groups of three conditions, we detected only small overlaps among the abiotic and hormone/chemical groupings. For example, abscisic acid, glucose, and osmotic stress had no overlapping respondents with increased expression and five shared respondents (1%) among those with decreased expression levels. Similarly, among the hormones abscisic acid, auxin, and jasmonic acid, one respondent (0.5%) had increased expression levels to all three treatments, and two (1%) had decreased expression. Cold, salt, and osmotic stress had no overlapping respondents with increased expression, and only one (0.5%) with decreased expression. However, the bacterial, fungal, and viral pathogens showed larger proportions of overlap with 111 (21%) shared respondents with increased expression levels and 83 (18%) with decreased levels.
Comparisons of sets of two treatments that are known to induce related physiological processes revealed more overlaps in RLK gene responses. We found that of the RLK genes with increased expression levels to abscisic acid and glucose, 38 (28%) of them responded to both. For those RLK genes with decreased expression levels to either glucose or abscisic acid, 68 (42%) displayed decreased levels for both. Gravity and auxin had nine (6%) shared respondents with increased expression, and nine (8%) with decreased expression. Abscisic acid and osmotic stress are also known to have cooperative effects in plant development (Zhu, 2002). Interestingly, we found that only one of the RLK genes (0.9%) displayed increased expression levels under both osmotic stress and abscisic acid. For genes with decreased expression levels to either abscisic acid or osmotic stress, seven (6%) had responses to both conditions. Plant responses to osmotic stress, salt stress, and cold are known to be intricately related (Mahajan and Tuteja, 2005). Surprisingly, osmotic stress and salt stress had no overlapping increased response, and an overlap of three (1%) RLK genes with decreased expression levels. Salt stress and cold had more shared responses, with six (10%) RLK genes with increased expression levels and 27 (19%) with decreased levels. Cold and osmotic stress had three shared respondents (5%) with increased expression, and 16 (8%) with decreased expression. Given the cross-talk that can occur in the signaling pathways involving abscisic acid, salt, and osmotic stress, the little overlap seen here may indicate that these genes are partitioned into condition-specific responses outside of those cross-talk networks. For example, it is known that the plant response to osmotic stress involves multiple signaling pathways, some of which are abscisic acid-dependent and some of which are abscisic acid-independent (Zhu, 2002). However, it also possible that temporal and tissue-specific differences may be influencing these results.
Among the biotic stress-related treatments, bacterial and viral pathogens shared more respondents than either bacterial–fungal pathogens or viral–fungal pathogens. The bacterial and viral pathogens had 231 (45%) shared respondents with increased expression levels, and 167 (44%) with decreased expression. In contrast, bacterial and fungal pathogens had 157 (32%) and 145 (34%) with increased and decreased expression levels, respectively, while fungal and viral pathogens had 146 (39%) increased and 128 (32%) decreased. Plant resistance to fungal pathogens is known to be related to jasmonic acid signaling (Kunkel and Brooks, 2002). Here, we found that fungal and jasmonic acid treatments produced 19 shared respondents (8%) with increased expression levels, and 20 shared respondents (7%) with decreased expression.
Overall, in looking at the three major classes of treatments—abiotic stress, biotic stress, and hormones/chemicals—we found that 48 RLK genes (9%) with increased expression levels and 83 (16%) with decreased expression levels were shared among the three (Figure 3B). While the results presented here have highlighted overlaps seen in responses to related treatments, it should be noted that this analysis additionally reveals those groups of RLK genes with distinct responses to specific treatments. Supplemental Table 3 lists all up-regulated and down-regulated RLK genes per treatment.
Molecular phylogenetic analysis of the amino acid sequences encoding the Arabidopsis RLK kinase domains has led to the classification of 43 RLK subfamilies plus one grouping of unclassified RLKs (UC), with most subfamilies also bearing distinct types and organization of sequence motifs in their extracellular domains (Shiu and Bleecker, 2001a). An appealing hypothesis is that each subfamily may service a specific, related set of physiological responses in plants (Shiu and Bleecker, 2001b). To investigate this question, we grouped the results of the expression analysis by subfamily and compared them across treatments (Figure 4A). Note that we also counted the responses found among the unclassified RLKs.
The mosaic plot depicted in Figure 4A is based on the number of differentially expressed RLK genes for a given subfamily under the specified treatment, scaled by the number of genes in the subfamily and the number of experiments related to the treatment. The area of each tile in the plot represents the joint distribution of differentially expressed genes for a given combination of subfamily and treatment. The lengths of each tile indicate the marginal distribution of differentially expressed genes per subfamily (vertical length) or treatment (horizontal length). Here, we find that the bacterial pathogen and abscisic acid treatments induced responses across all subfamilies. To a lesser extent, the fungal and viral pathogens, as well as glucose, had near widespread effects. It is also interesting to note the amount of distortion in the tiles for the abiotic stress-related treatments and for jasmonic acid, which suggests associations between subfamilies and these treatments in terms of the number of differentially expressed members.
Figure 4B depicts the proportion of each subfamily's total number of responses according to the three major classes of treatments: abiotic stress, biotic stress, and hormones/chemicals. The plot in Figure 4B reveals that, in general, a slightly larger proportion of each subfamily's responses are found under abiotic stress and hormone/chemical treatments, with a smaller proportion induced by the biotic stress conditions. However, for certain subfamilies, such as PERKL, SD-2, and Thaumatin, the effects were more evenly distributed.
In absolute terms, the number of responses varied for each subfamily, with the DUF26 and LRR III subfamilies each registering the largest number at 207, while the C-Lectin and SD-3 subfamilies each had the smallest number at six. We found that overall, every RLK subfamily displayed responses to a broad range of treatments, with the smallest number of treatments being five (the RKF3L subfamily) and 13 of the subfamilies showing at least one differentially expressed member to all 12 of the treatments. Based on these results, it is clear that each RLK subfamily contains members that are responsive to different types of signals, as opposed to a specific type of treatment.
In the previous analysis, we found that each RLK subfamily had members that were differentially expressed under different types of treatments. Next, we investigated the extent to which expression profiles diverge or overlap among the RLK genes, particularly within the 43 subfamilies. Dissimilar expression patterns may be indicative of functional divergences among closely related RLK members, while similar expression patterns may indicate the presence of functional overlaps. Such redundancies have been reported for several of the RLKs (Shiu and Bleecker, 2001b; Johnson and Ingram, 2005; Dievart et al., 2003). For example, three members of the LRR XIII subfamily have been shown to have functional overlaps through the analysis of a triple mutant (Shpak et al., 2004). The presence of such overlaps was also offered as a plausible explanation for the difficulty often encountered in generating identifiable phenotypes in single loss-of-function RLK mutants.
To analyze whether expression patterns appear to be conserved or divergent within each subfamily, we measured the distance between RLK gene expression profiles across the arrays used in our study in pairwise fashion, using a metric based on the Pearson correlation coefficient (r) (see Methods). The final gene expression distance for a subfamily represents the median of the pairwise distances (dr) among all of its members, using a normalized scale of 0 to 1, with 1 being most distant. Based on this analysis, we found that the level of expression divergence varied widely among the RLK subfamilies (Figure 5). The largest divergence, seen in the RLCK XI subfamily (median dr=0.55), was approximately three times that of the smallest divergence, registered by the CrRLK1L-2 subfamily (median dr=0.18). Note that these results apply only to those subfamilies with two or more members and therefore exlude the C-Lectin and SD-3 subfamilies.
However, we also found that, for the most part, the majority of subfamilies exhibited a broad range of distances among their expression profiles, which we calculated by subtracting the lowest pairwise dr value from the highest for each subfamily. The smallest dr range was 0.10, found in the RLCK X subfamily, and the CrRLK1L-1 subfamily had the largest dr range at 0.75. The average dr range for all subfamilies was 0.48. To ensure that the subfamily expression distances were not an artifact of membership size, we checked the correlation of the median expression distance of each subfamily to its membership size and found no significant correlation (r=0.05).
We also looked at the expression profile distances among the three LRR XIII subfamily members with known functional overlaps (Shpak et al., 2004). We found that their expression profiles were indeed similar, with pairwise distances of dr=0.18, dr=0.21, and dr=0.32 among the three. In a ranking of all distances generated in our analysis from shortest to longest, these distances fell into the 97th, 96th, and 85th percentiles, respectively. Supplemental Dataset 1 contains a list of all the pairwise distances between subfamily members for each subfamily.
The broad range of distances found among the expression profiles within each subfamily led us to ask whether associations existed between expression profiles of different subfamilies. On a functional level, interactions between different subfamily members have been shown to occur, for instance, with members of the LRR II and LRR X subfamilies (Nam and Li, 2002; Li et al., 2002). To perform this analysis, we used the subfamily classification scheme as an a priori clustering of the expression profiles and calculated the silhouette widths (si) for all members of each subfamily (Figure 6A) (Kaufman and Rousseeuw, 1990). In this case, the silhouette width measures how closely associated an individual expression profile is to those found in its own subfamily, compared to profiles from other subfamilies.
Our results show that the majority of RLK genes had associations outside of their own subfamily, as represented by the negative silhouette width scores in Figure 6A. Furthermore, the silhouette width average for the entire a priori clustering was siD=–0.26. These results show that the expression profiles do not cluster well according to subfamily. For the most part, each subfamily had widely disparate expression profiles, so much so that they appear to have associations outside of their subfamily to a greater degree than within their own subfamily. This result is consistent with the notion that the activity of the genes in each subfamily are related to divergent physiological processes, as suggested in Figure 4A and 4B.
Next, we attempted to separate the data into groups of conserved expression profiles, regardless of subfamily membership. To do so, we used a clustering approach called Partitioning Around Medoids (PAM), and calculated the silhouette widths for the resulting cluster structure. PAM clusters data by first identifying the best K medoids in the data, and then assigning all other observations to its nearest medoid (Kaufman and Rousseeuw, 1990). In this case, we used PAM to find the best 43 clusters (K=43), matching the number of RLK subfamilies minus the unclassified grouping. In the resulting cluster structure, we found no support for the PAM-derived clusters based on an overall silhouette width average of siD=0.09 (Figure 6B). However, two interesting points emerged from the silhouette plot of the PAM clustering. First, the composition of each cluster was typically a heterogeneous mix of subfamily types. This result suggests the possibility of widespread interactions among different RLK genes. Second, the results show that, for the conditions tested, the responses to a particular treatment may involve the activity of an assortment of RLK genes.
We also tested a range of cluster numbers (K=2 to K=50) in our PAM analysis but the results indicated that no ideal number could produce silhouette width measures that strongly supported the clustering (siD>0.5) (Supplemental Figure 1). Finally, we used the Hierarchical Ordered Partitioning and Collapsing Hybrid (HOPACH) algorithm as a second attempt to cluster the expression profiles but found a similar lack of support for the HOPACH clustering (25 clusters, siD=0.06, Supplemental Figure 2) (van der Laan and Pollard, 2003).
Given that our analysis found a high level of associations between expression profiles from different subfamilies, as seen in Figure 6A, we used hierarchical clustering to view subfamily relationships according to the average expression profile distances among them (Figure 7). The clustering itself was based on average linkage between subfamilies and resulted in a dendogram with three major clusters. Interestingly, nine of the 14 LRR subfamilies are found in the first cluster, and the 10 RLCK subfamilies appear to be distributed across the clusters. Taken together, the clustering and silhouette width analyses reveal a high level of diversity in the RLK transcriptional response, with complex associations found among different groupings of profiles and across RLK subfamilies. Supplemental Dataset 2 contains a list of gene expression distances across subfamilies, as well as a summary of the clustering and silhouette width analyses, including cluster associations, nearest neighboring clusters, and silhouette width measures for each RLK.
To investigate whether there was a sequence basis for the levels of expression profile divergence seen within each RLK subfamily, we asked whether subfamily members with similar sequences exhibited similar expression profiles, and, conversely, whether less similar sequences had more divergent expression profiles. In order to answer this question, we performed all-against-all pairwise alignments of RLK amino acid sequences, using ClustalW and the Gonnet series of scoring matrices (Thompson et al., 1994; Gonnet et al., 1992). From each pairwise alignment, we calculated a distance based on the normalized alignment score. As with the expression profile distances, the sequence distances (dseq) fall between 0 and 1, with 1 being most distant. Overall, the median sequence distances for all within-subfamily comparisons varied (Figure 8A).
Next, for each subfamily, we extracted the sequence and expression profile distances for all within-subfamily pairwise comparisons and calculated the correlation between the two sets of values. We found that of the 38 subfamilies, 20 (53%) exhibited a correlation (r≥0.2 or r≤–0.2) between sequence similarity score and expression profile distance (Figure 8B). Note that five subfamilies (C-Lectin, CrRLK1L-2, RKF3L, SD-3, and URK I) had two or fewer members and could not be included in the analysis. In addition, we did not include the unclassified RLKs.
Within these 20 subfamilies, we found two distinct, though vastly different, sets of results. Sixteen of the subfamilies exhibited a positive correlation (r≥0.2), indicating that the closer the sequence similarity among subfamily members, the more conserved their expression profiles. Perhaps more intriguingly, four of the subfamilies displayed a negative correlation (r≤–0.2) between sequence and expression. In this case, the more similar the sequences within the subfamily, the more distant their expression profiles. We also checked whether the correlation between sequence distance and expression profile distance was affected by subfamily size and found no such correlation (r=–0.03). In addition, we found no overall correlation between sequence distance and expression profile distance for the RLK superfamily as a whole (r=–0.02).
Based on our analysis of amino acid sequence and expression profile distances, it appeared that different evolutionary forces might be related to the divergence of expression patterns seen within the RLK subfamilies. For this reason, we formally investigated whether a link existed between RLK sequence evolution and expression divergence. Recent studies have paired molecular phylogenetic methods with expression profiling to investigate the evolutionary and functional implications of gene expression divergences (Nuzhdin et al., 2004; Akashi, 2001; Wagner, 2000). In particular, studies have looked at measures of sequence divergence and selective pressure among both orthologous and paralogous genes and compared them to similarities seen in their expression patterns, in order to make initial assessments of functional evolution among the sequences (Good et al., 2006; Oakley et al., 2005; Lemos et al., 2005).
In our case, to discern whether evolutionary events might have had an effect on RLK subfamily expression profiles, we first attempted to establish whether members of the subfamilies displayed signs of selective pressure. To do so, we calculated the ratio of non-synonymous-to-synonymous substitution rates, the so-called dN/dS ratio, among the sequences using the method of Yang and Nielsen (2000). The dN/dS ratio (ω) provides a measure of whether the molecular sequences in question appear to be under negative (purifying) selection or positive (diversifying) selection. For each subfamily, we created multiple amino acid sequence alignments of its members, and used these alignments to guide the alignment of their coding DNA (see Methods). From the aligned DNA sequences, we calculated the dN/dS ratios for all pairwise comparisons within each subfamily using the yn00 program in PAML (Yang, 1997). We then calculated the median dN/dS ratio for each subfamily, as well as the range of all ratios found within each subfamily (Figure 9A).
Based on this analysis, we found that none of the subfamilies as a whole showed signs of positive selection (ωmed>1). In fact, the median values for all subfamilies were less than ωmed=0.40, indicating that the majority of the sequences were under varying degrees of negative selection. Interestingly, one of the subfamilies, LRR III, contained 13 members that showed signs of positive selection (ω>1), although the median ratio for the subfamily was ωmed=0.37. Similarly, the DUF26 subfamily had a pair of members with a ratio nearing ω=0.98, where ω=1 is often interpreted as selectively neutral conditions.
Although the RLK subfamilies appear to have evolved under negative selection, variations in the strength of selection might have had an impact on expression divergence within each subfamily. For this reason, we tested whether the degree of selective pressure as measured by ω had any relationship to the amount of expression divergence seen within each subfamily. To test for this, we calculated the correlation between all pairwise dN/dS ratios and their corresponding pairwise expression profile distances within each subfamily (Figure 9B). Of the 38 subfamilies analyzed, we found that 14 (37%) had correlations of either r≥0.2 or r≤–0.2. Eight of the 14 subfamilies (Extensin, LRK10L-1, LRR VII, LRR XII, LRR XIII, RLCK IV, RLCK XI, and Thaumatin) show a positive correlation between dN/dS and their expression divergence. That is, the more relaxed the negative selection, the more divergent their expression profiles. In contrast, the remaining six subfamilies (LRR IV, LRR VIII-2, LRR IX, RLCK I, RLCK III, and SD-1) show a negative correlation in which sequences under greater negative selective pressure had greater divergence in their expression profiles.
Next, we used the synonymous substitution rate (dS) as a measure of divergence time found among RLK subfamily members, and calculated the correlation of this measure with expression divergence (Figure 10A and 10B) (Gu et al., 2002). We found that of the 38 subfamilies, 11 (29%) had correlations of either r≥0.2 or r≤–0.2. Seven of the subfamilies (LRK10L-1, LRR I, LRR II, LRR VIII-2, LRR IX, RLCK I, and RLCK III) had a positive correlation between divergence time and expression divergence among its members. Four of the subfamilies (LRR VII, LysM, RLCK IV, and RLCK X) registered a negative correlation between divergence time and expression divergence. We also checked to ensure that subfamily size did not influence the correlation between dN/dS and expression divergence and found no such effect (r=–0.01), and found only a slight association (r=0.10) between dS and family size.
Finally, to look at the general trends in the relationships among divergence time (dS), sequence distance (dseq), expression distance (dr), and selective pressure (dN/dS) at the subfamily level, we plotted the median values for each subfamily in a four-way scatter plot matrix (Figure 11). Measured at the level of the subfamily, it appeared that divergence time and sequence distance had a very weak association (r=0.12), as did sequence distance and expression distance (r=0.12). Divergence time and expression distance as a whole appeared unrelated (r=–0.03), as did selective pressure and expression distance (r=0.05). Finally, sequence distance and selective pressure had a positive association (r=0.35), and, as expected, divergence time and selective pressure were negatively associated (r=–0.63).
The genome of Arabidopsis thaliana contains more than 600 receptor-like kinase genes, the great majority of which have yet to be investigated experimentally. Here, we have created a detailed expression profile of 604 receptor-like kinase genes after exposure to a cross-section of major developmental and environmental signaling factors in plants, including abiotic stresses, biotic stresses, and hormones. Our results show that RLK gene activity is regulated at the transcriptional level in response to many of these factors and suggest that a great number of RLKs may be functionally relevant components of a broad spectrum of essential signaling processes in plants. Furthermore, these results specifically identify those signaling conditions that elicit changes in RLK transcriptional levels on a gene-by-gene basis, as well as similarities and divergences in expression among closely related RLK genes.
These results are significant in that, prior to the detection of the first receptor-like kinase in maize, it was believed that the primary mechanism for signaling in plants was the symplastic transit of molecules through the intracellular tubules known as plasmodesmata (Dievart and Clark, 2004; Walker and Zhang, 1990). The discovery of RLKs as large gene families in land plants changed this conception and provided a new focus for research into plant extracellular signaling (Shiu and Bleecker, 2001a). However, although ongoing experimental analyses have bolstered the hypothesis that RLKs are involved in signaling pathways that service fundamental plant physiological processes, breakthroughs in identifying these pathways have been limited to a relatively small subset of individual RLKs. By taking a functional genomics approach to investigate this hypothesis, we have generated a large body of initial evidence as to RLK functionality in Arabidopsis for the complete genomic inventory of RLKs. Additionally, the preponderance of changes that we found in the RLK transcriptome further supports the widely held belief that RLKs are major contributors to the processing of a vast array of plant developmental and environmental cues.
Our results also extend the initial observation that transcriptional regulation may serve as an important mechanism for controlling RLK-mediated responses. Previous reports have implicated post-translational events at the biochemical and cellular level as possible forms of regulating RLK activity. For instance, receptor oligomerization and hyperphosphorylation have been demonstrated in several of the well studied RLKs, including BRI1, BAK1, and SYMRK (Nam and Li, 2002; Li et al., 2002; Wang et al., 2005; Yoshida and Parniske, 2005). In addition, receptor internalization and dephosphorylation were exhibited by ACR4, SERK3, and BRI1 (Russinova et al., 2004; Gifford et al., 2005). A third possible form of regulation was speculated to occur at the transcriptional level. Initial evidence demonstrated clear changes in the gene expression of several RLKs in response to signaling factors such as abscisic acid, salicylic acid, oxidative stress, and light (Shiu and Bleecker, 2001b; Becraft, 2002). Our results greatly expand on this evidence and indicate that transcriptional regulation may be an important form of controlling the activity of a large number of RLK genes in a wide variety of signaling events. As an obvious advancement of this result, it will be critical to establish the relationship between the transcriptional response of a given RLK gene and the functional response provided by its gene products.
Our study also revealed that the transcriptional levels of many RLK genes are affected by more than one signaling factor. These results support current models of RLK versatility that have been reported recently. In one study, an RLK homologue in tomato, tBRI1/SR160, appeared to be capable of sensing both steroid and peptide hormones, and subsequently functioning in distinct signaling pathways (Montoya et al., 2002). A second form of versatility was demonstrated in BRI1, an Arabidopsis RLK, which was able to either homodimerize or interact with another RLK, BAK1, under differing conditions (Wang et al., 2005; Russinova et al., 2004; Wang et al., 2005). The ERECTA RLKs also appear to be capable of differential interactions in response to different ligands (Johnson and Ingram, 2005; Shpak et al., 2005). Given that most of the insights into RLK mechanics revolve around a few individual RLKs, the extent that such versatility exists among the large contingent of unexplored RLKs is unknown. However, in light of these models, our results highlight a number of RLK genes that may be involved in multiple signaling pathways, and suggest that such functional versatility may be a widespread feature of the RLKs.
Another explanation for the multiplicity of responses seen among the RLKs is that an individual RLK may be a component of a secondary response that exists downstream of separate signaling pathways. This interpretation is particularly appealing for those RLKs whose transcriptional levels were regulated by treatments known to induce physiologically related responses in plants. In particular, it would explain the widespread response, as well as the great degree of overlap, seen in the bacterial, fungal, and viral pathogen assays. Although the initial signaling events differ among these stimuli, they are known to target a number of related downstream pathways within the infected host, including those involved in the hypersensitive response, systemic acquired resistance, and the de-novo generation of additional signaling molecules, such as hydrogen peroxide and nitrous oxide (Kunkel and Brooks, 2002). This interpretation, although likely, remains to be demonstrated. In addition, the forms of RLK signaling versatility mentioned here are not mutually exclusive; these mechanisms may all be represented in the functional repertoire of the RLK superfamily.
The potential for complex signaling responses seen among individual RLKs is further enhanced when considered at the subfamily level. Previously, it had been speculated that, due to the differential configurations of their extracellular domains, members of each subfamily might be involved in similar signaling pathways. Here, we have shown that each subfamily exhibited transcriptional responses to a diverse set of signal types. The targeting of signals, such as hormones, to different members of the same gene family is a known phenomenon in plants (Nemhauser et al., 2006). In the case of RLKs, it may be that, within a given subfamily, individual members have roles in disparate signaling events. However, the diversity of responses seen within each subfamily may also indicate a mechanism by which different types of signals may be perceived by specific members of the same subfamily, yet induce similar downstream signaling events. This mechanism would allow for the integration of multiple signaling inputs in forming a finely tuned physiological response to complex environmental conditions.
As noted in the literature, a major problem in determining RLK functionality has been the frequent inability to establish phenotypes in single loss-of-function genetic lines (Johnson and Ingram, 2005). One factor possibly contributing to this problem was the lack of physiologically relevant screening conditions (Shiu and Bleecker, 2001b). However, a second factor cited was the likely existence of functional redundancies among similar RLKs (Shiu and Bleecker, 2001b; Dievart and Clark, 2004; Shpak et al., 2003). A common use of microarray data is to predict functional similarities and interactions among genes by looking for similarities in their expression patterns (Walker et al., 1999; Hughes et al., 2000). This concept has been the basis for active areas of research in clustering and classification methods, as well as in terms of biological discovery, such as inferring regulatory networks and signaling pathway components.
The results of our work provide a detailed expression profile of each RLK gene not only in response to a range of screening conditions, but in relationship to genes both within its own subfamily and across other RLK subfamilies. The conserved expression profiles within each subfamily—particularly from genes with high sequence similarity—are obvious candidates for functional redundancies. Curiously, we also found a great degree of expression similarity between members from different subfamilies. This result suggests that functional relationships may also be common among members of separate subfamilies. Such a phenomenon has been experimentally demonstrated in the interaction of a member of the LRR X subfamily, BRI1, with a member of the LRR II subfamily, SERK1II/BAK1 (Nam and Li, 2002; Russinova et al., 2004). It should be noted, however, that our data do not capture tissue-specific divergences that may exist among the expression patterns. Although functional overlaps may exist among those RLKs with similar expression patterns, they may not always result in redundancy if expression is restricted to discrete domains. Nonetheless, the datasets we provide allow future experimental designs to account for possible complementarity or interactions among such similarly expressed RLK genes.
The diversity of expression profiles we found within each subfamily may also explain the expansion and retention of RLK genes within the Arabidopsis genome. Previous analyses support the hypothesis that gene duplication played a major role in the appearance of the multi-member RLK subfamilies in Arabidopsis (Shiu et al., 2004; Morillo and Tax, 2006; Becraft, 2002). It is thought that one key to retaining such duplicates is through functional diversification, and that divergence in gene expression may be a primary step in this process (Gu et al., 2002; Ganko et al., 2007). Here, we found a high level of divergent expression among RLK subfamilies, and we investigated possible evolutionary dynamics underlying this divergence.
In our analysis of selective pressure on the RLKs, we found that all of the subfamilies appear to be under some degree of purifying selection when considering the ratio of non-synonymous-to-synonymous substitution rates for full-length sequences within each subfamily. It should be noted that others have reported finding signs of positive selection at specific sites within the extracellular domains of some RLK subgroups (Shiu et al., 2004; Verica et al., 2003; Strain and Muse, 2005; Zhang et al., 2006). However, we did find that the strength of purifying selection varied among the subfamilies and that about a third of the subfamilies displayed some degree of association between selective pressure and expression divergence. The positive association found among eight of the subfamilies may reflect a dynamic in which relaxed purifying selection may have allowed for greater divergence in expression to evolve (Good et al., 2006; Gu et al., 2002; Zhang, 2003). Interestingly, we found that six of the subfamilies had an inverse association between selective pressure and expression divergence. In these cases, even those sequences under greater selective pressure relative to other members of its subfamilies were able to diverge in expression.
Finally, we compared expression divergence to two measures of the amount of sequence evolution found among subfamily members: sequence distance (dseq) and sequence divergence time (dS). In terms of expression distance, we found 20 of the subfamilies (53%) displayed some association with sequence distance, and 11 of the subfamilies (29%) showed an association with sequence divergence time. Given that seven of the subfamilies overlapped between these results, 24 of the 38 subfamilies (63%) we analyzed, representing 251 of the 604 RLK genes (42%), showed signs of an association between sequence evolution and expression divergence. Eighteen of the subfamilies (47%), representing 220 RLK genes (36%), had a positive association in which more diverged sequences had higher levels of expression divergence. Interestingly, six of the subfamilies (16%) representing 31 RLK genes (5%) had an inverse association in which the more closely related sequences had the more divergent expression patterns. In either case, it may be that the great amount of expression divergence seen within the individual RLK subfamilies served as a primary mechanism for maintaining such an expansive number of RLK genes in the Arabidopsis genome (Gu et al., 2002; Ganko et al., 2007). However, as our results suggest, although many paralogs within the RLK subfamilies have been retained, it appears that distinctly different evolutionary processes might have determined their fates.
The data presented in this study were generated from 68 individual experiments coordinated by Syngenta, Inc., using the Syngenta custom Arabidopsis GeneChip array (sysSYNG002a, Affymetrix, Santa Clara, California, USA). Note that data produced in these experiments passed manual quality examination and datasets representing different areas of focus from the one presented here have been published (see Supplemental Table 1). Experimental parameters from these experiments, including details of treatments, dosages, and tissues, are described in Supplemental Table 1. Subsequent cDNA synthesis and hybridization were performed as described by Zhu et al. (2001).
CEL files from each experiment were processed by a uniform algorithm (Zhu and Wang, 2000) and signal readings were globally scaled across each array to an arbitrarily defined target value (Zhu et al., 2001). The expression indices of 604 known and predicted RLK genes (Shiu and Bleecker, 2001a) represented on the GeneChip array were extracted and paired as control and treated samples according to experimental design. For each experiment, any gene with an average difference (signal reading) of less than 5 in either or both the control or treatment sample were disregarded (Chen et al., 2002; Zhu et al., 2001). Signal log2 ratios were generated by taking the ratio of the treatment signal reading to the control signal reading and performing a log2 transformation (Chen et al., 2002).
Note that, in each experiment, the samples were pooled from at least eight individual plants receiving the same treatment (or mock treatment) in order to control for biological variation. Consequently, the detected mRNA levels represent an average reading of the biological replicates. To ensure data quality and stability in the analyses, the biological reproducibility of the samples was tested by performing 11 experiments with biological replicates. The results showed a high level of correlation among the replicated experiments, with each compared experimental results having a correlation of r>0.90.
Because the complexity and diversity of experimental designs represented in the dataset did not allow for explicit modeling of variation among biological replicates across all conditions, we were restricted to using a heuristic approach to identifying changes in gene expression. Consequently, we sought to impose relatively stringent criteria for classifying differentially expressed genes. In this case, we chose a two-fold cut-off based on a preliminary analysis of false-positive rates, in which the false-positive rate at a two-fold threshold was demonstrated to be 0.2% (Zhu and Wang, 2000). Finally, an exhaustive, secondary confirmation of all gene expression changes under all conditions in this study was not tractable. However, an independent set of experiments based on RNA gel analysis have confirmed the GeneChip data for a subset of genes and conditions presented here (Zhu et al., 2001).
To measure similarity among expression profiles, we concatenated 104 arrays from our study and created a matrix of normalized signal readings for the 604 RLK genes. An expression profile for a given gene was represented by its vector of signal readings across the 104 arrays. To calculate gene expression distances between any two genes, we first computed the mean-centered Pearson product-moment correlation coefficient (r) between the expression vectors X and Y of the genes, where i represents the array number and N the total number of arrays:
The distance in gene expression between any two genes i and j was then calculated as:
In the process of determining correlation values, if a signal reading for either gene from a particular array was below 5, we removed the array for that particular comparison.
Once the distances were computed for all pairwise comparisons within the matrix (182106 comparisons in total), we normalized the distances by dividing each distance between any two genes i and j by the largest value found in the resulting dataset:
This normalization transformed the distances to a scale of 0 to 1, with 1 being most distant. In parsing the dataset into subfamily-based comparisons, we followed the subfamily classification scheme designated by Shiu and Bleecker (2001a).
The RLK gene expression profiles were clustered in two ways for analysis. The first clustering consisted of the manual separation of the 604 expression profiles into 43 a priori clusters based on the noted subfamily classification scheme (Shiu and Bleecker, 2001b). The second clustering was performed using the R implementation of the Partitioning Around Medoids (PAM) algorithm (Kauffman and Rousseeuw, 1990). Given a set of K medoids, PAM clusters observations by assigning each observation to its nearest medoid. The K medoids selected by the algorithm minimize the sum of the distances of each observation from its nearest medoid. Forty-three clusters were specified for the PAM clustering to correspond with the number of subfamily clusters.
Silhouette widths were calculated for the a priori clustering and the PAM clustering (K=43). The same distance matrix based on the Pearson correlation (dr) was used to calculate silhouette widths for each clustering approach. The silhouette width (si) of a given observation i is defined as:
where ai represents the average distance of i to all other observations in its cluster, and bi represents the average distance of i to the observations in its nearest neighboring cluster. The average silhouette width for a cluster (siC) is the average of the silhouette widths for all members of a cluster. The average silhouette width for a cluster structure (siD) is the average of all silhouette widths in the dataset.
The Hierarchical Ordered Partitioning and Clustering Hybrid (HOPACH) algorithm was also used as a potential clustering method. HOPACH combines hierarchical clustering with partitioning, creating a data-adaptive tree that is composed of partitions at each level K. The optimal number of child clusters in partitioning steps, as well as the optimal number of clusters to be joined in collapsing steps, rely on the mean or median split silhouette measure of cluster heterogeneity (van der Laan and Pollard, 2003). For a given number of clusters k, a partitioning clustering method (in this case, PAM) is applied to each cluster. The split silhouette is defined as the maximum average silhouette width when the partitioning clustering method is applied to the elements of cluster k only. The mean split silhouette is the average of the split silhouettes over all clusters.
We created an initial distance matrix containing the normalized expression distances (dr) for all pairwise comparisons among 585 RLK genes, with the 19 unclassified RLK genes removed from the dataset. Then, for each comparison between subfamilies, we averaged the expression distances found between their members to create a 43-by-43 subfamily distance matrix. We performed hierarchical clustering on the subfamily distance matrix using the hclust function provided by the stats package in R (version 2.6.2, www.r-project.org). hclust relies on an agglomerative algorithm in which each initial object (here, subfamilies) is assigned to its own cluster. The two most similar clusters in the matrix as measured by average gene expression distance are then joined and distances between the new cluster and all remaining objects are re-calculated. In our implementation, we used an average linkage method to update distances, in which the new distances are calculated based on the average distances between members of separate clusters. Consequently, the dendogram depicted in Figure 7 represents an average-linkage hierarchical clustering of subfamilies based on average-linkage gene expression distances.
We extracted amino acid sequences representing the 604 Arabidopsis RLKs from the NCBI GenBank protein database (www.ncbi.nlm.nih.gov) using the AGI identifiers provided by Shiu and Bleecker (2001a). Supplemental Table 5 contains a map of the AGI and GI identifiers and subfamily classification for all RLKs used in this study. In determining distances among these sequences, we first used sequence alignment scores (si,j) as a measure of similarity. The alignment scores were computed by performing all-against-all pairwise alignments (182106 in total) among the set of 604 RLK sequences. The alignments and scores were generated by ClustalW (version 1.83) and the Gonnet series of substitution matrices, with gap open and extension penalties of 10.0 and 0.1, respectively (Thompson et al., 1994; Gonnet et al., 1992).
To convert the alignment score between any two sequences i and j into a sequence distance, we normalized each score using the maximum value found among all observations and subtracted it from 1:
Correlations between sequence distances and expression distances were calculated for each subfamily by comparing dseq and dr for matching sets of pairwise comparisons over all comparisons within each subfamily, using the Pearson product-moment correlation coefficient.
We retrieved nucleotide sequences representing coding DNA for 585 RLKs from the Arabidopsis Information Resource website (TAIR, www.arabidopsis.org), excluding those RLK genes that remain unclassified. We divided the RLK protein and nucleotide coding sequences into 43 subfamilies based on the classification scheme designated by Shiu and Bleecker (2001b). For each subfamily, we produced a multiple protein sequence alignment using the program MUSCLE (version 3.6) (Edgar, 2004). Based on the multiple protein sequence alignment, we then created a multiple sequence alignment of the coding DNA for all members of each subfamily. In some cases, extremely long or short sequences caused the inclusion of a high number of gaps in the protein sequence alignment, which resulted in very short DNA alignments. When this occurred, the long/short sequences were removed from further analysis and the protein and nucleotide sequences were re-aligned. Overall, three subfamilies were affected by this modification: LRK10L-2 (two of eight sequences removed), LRR VIII-2 (five of 14 sequences removed), and PERKL (four of 19 sequences removed).
For each subfamily, dS and dN/dS were calculated for each pairwise comparison of codon alignments within the subfamily using the yn00 program in the PAML package (Yang and Nielsen, 2000; Yang, 1997). Codons aligned to gapped regions in the alignment were removed during this process. When normalizing these measures, we divided each value by the highest measurement found across all subfamilies. For each type of measurement, correlations with normalized expression profile distances were calculated for matching sets of pairwise comparisons over all comparisons within each subfamily, using the Pearson product-moment correlation coefficient.
The mosaic and box plots depicted in the manuscript were created using the mosaicplot and boxplot functions provided by the graphics package in R (version 2.6.2). The scatter plot matrix was produced in R using the car package (version 1.2-7). The silhouette plots were generated using the plot function on silhouette objects created both by custom R code and by the silhouette function found in the cluster package in R (version 1.11.10).
Supplementary Data are available at Molecular Plant Online.
Supplemental Table 1. Description of Microarray Experiments and List of Related Publications.
Supplemental Table 2. List of Differentially Expressed RLK Genes for All 68 Experiments, Grouped by Experiment.
Supplemental Table 3. Table of Differentially Expression RLK Genes per Treatment, Separated into Up-Regulated and Down-Regulated Responses.
Supplemental Table 4. Index Listing the AGI and GI Identifiers and Subfamily Classification for Each of the 604 RLKs Analyzed in the Study.
Supplemental Dataset 1. Normalized Pairwise Expression Distances between Subfamily Members for Each Subfamily.
Supplemental Dataset 2. Files Containing Normalized Expression Profile Distances across Subfamilies and Summaries of the Clustering and Silhouette Width Analyses.
Supplemental Figure 1. Average Silhouette Widths for PAM Clustering of RLK Expression Profiles across Different Values of K.
Supplemental Figure 2. Silhouette Plot for HOPACH Clustering of RLK Expression Profiles.
Funding for this work was provided by a grant from the National Science Foundation (award to S.L.). L.C. is also supported in part by funding from the California Agricultural Experimental Station (to S.L. and Steven Brenner).