http://orcid.org/0000-0001-9254-0730
Figures
Abstract
Despite identification of WRKY family genes in numerous plant species, a little is known about WRKY genes in watermelon, one of the most economically important fruit crops around the world. Here, we identified a total of 63 putative WRKY genes in watermelon and classified them into three major groups (I-III) and five subgroups (IIa-IIe) in group II. The structure analysis indicated that ClWRKYs with different WRKY domains or motifs may play different roles by regulating respective target genes. The expressions of ClWRKYs in different tissues indicate that they are involved in various tissue growth and development. Furthermore, the diverse responses of ClWRKYs to drought, salt, or cold stress suggest that they positively or negatively affect plant tolerance to various abiotic stresses. In addition, the altered expression patterns of ClWRKYs in response to phytohormones such as, ABA, SA, MeJA, and ETH, imply the occurrence of complex cross-talks between ClWRKYs and plant hormone signals in regulating plant physiological and biological processes. Taken together, our findings provide valuable clues to further explore the function and regulatory mechanisms of ClWRKY genes in watermelon growth, development, and adaption to environmental stresses.
Citation: Yang X, Li H, Yang Y, Wang Y, Mo Y, Zhang R, et al. (2018) Identification and expression analyses of WRKY genes reveal their involvement in growth and abiotic stress response in watermelon (Citrullus lanatus). PLoS ONE 13(1): e0191308. https://doi.org/10.1371/journal.pone.0191308
Editor: Sara Amancio, Universidade de Lisboa Instituto Superior de Agronomia, PORTUGAL
Received: September 29, 2017; Accepted: January 2, 2018; Published: January 16, 2018
Copyright: © 2018 Yang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: The present study was financially supported by grants from the Earmarked Fund for Modern Agro-industry Technology Research System of China (CARS-25), the Science and Technological of Shaanxi Province (2015KTTSNY03-04), the Scientific Startup Foundation for Doctors of Northwest A&F University (Z109021604), the Basal Research Foundation of Northwest A&F University (Z109021612) and the Key Project of Shaanxi Province (2017ZDXM-NY-025). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Transcription factors (TFs) play an essential role in regulating the transcription of specific target genes by binding to their promoters. The WRKY gene family is one of the 10 largest transcription factor families in plants [1]. Typically, proteins in this family possess one or two highly conserved WRKY domains which include a conserved WRKYGQK heptapeptide at N-terminus and a distinctive zinc-finger like motif C2H2 or C2HC at C- terminus [2, 3]. To regulate gene expression, the WRKY domain binds to the cis-acting element W box (TTGACC/T) in the promoter of the target gene [4]. In addition to W box, WRKY proteins can also bind to other elements, such as a sugar-responsive (SURE) cis-element (TAAAGATTACTAATAGGAA) and a pathogen-responsive element PRE4 (TGCGCTT), indicating the multiplicity in the mechanism of their functions [3].
Since the first cloning and characterization of the WRKY cDNA, SPF1 from sweet potato [5], numerous WRKY gene families have been analyzed from more than 100 other plant species [6]. In Arabidopsis, 72 WRKY genes were classified into three groups I-III based on the number of WRKY domains and the features of their zinc-finger structure [2]. Group I proteins contain two WRKY domains, one at the C- and the other at the N-terminus, whereas group II and group III proteins only contain one single WRKY domain at N-terminus. Both group I and group II proteins have the same pattern of potential zinc ligands (C-X4-5-C-X22-23-H-X-H), while, Group III proteins contain one C2-H-C zinc-finger motif. Furthermore, group II proteins can be accurately divided into five subgroups (IIa+b, IIc, IId+e) based on the phylogenetic data of the WRKY domains [2, 7]. Phylogenetic analysis has proven that the groups II and III originated from the oldest group I proteins [7, 8], and the group II genes are not monophyletic [3]. In addition, genomic comparison from a model species to a less-studied species can provide important information on the expansion and the evolution of the WRKY gene families in plants [9].
Numerous studies have established the important roles of WRKY proteins in various physiological processes such as seed germination [10], lateral root formation [11], flowering time [12], fruit ripening [13], leaf senescence [14], and metabolic processes as well [15, 16]. WRKY proteins also play important regulatory roles in plant defense against various biotic and abiotic stresses, such as pathogens, nutrient deficiency, UV-B, heavy metals, salinity, drought and cold stress [17–19]. For instance, overexpression of BnWRKY33 enhances resistance to Sclerotinia sclerotiorum in transgenic oilseed rape [20], while, double mutants of AtWRKY54 and AtWRKY70 in Arabidopsis clearly show enhanced tolerance to osmotic stress due to improved water retention and stomatal closure [21]. Notably, the regulatory roles of WRKY proteins are closely associated with multiple plant hormone-mediated signal pathways. In rice, various phytohormone treatments significantly alter expression patterns of 54 WRKY genes [22]. AtWRKY50 and AtWRKY51 work as positive regulators in the salicylic acid (SA) signaling pathway but as negative regulators in jasmonic acid (JA) signaling [23]. Increasing number of studies show that abscisic acid (ABA) signaling pathway is involved in the WRKY proteins-mediated responses of plants to various abiotic stresses [24–26].
The watermelon (Citrullus lanatus (thunb.) Matsum. & Nakai) is one of the most economically important fruit crops in the world. According to FAOSTAT2014, watermelon is cultivated all over the world with total area of 3.48 million hectares and annual production of 11.10 million tons, making it among the top five most consumed fresh fruits (http://www.fao.org/). Since a high-quality draft genome sequence of the East Asia watermelon cultivar 97103 has been reported [27], many transcription factors including mitogen-activated protein kinase (MAPK), no apical meristem-ATAF1/2-cup shaped cotyledon (NAC), and nuclear factor Y (NF-Y) have been subsequently identified and analyzed in watermelon [28–30]. However, there is still little information about WRKY genes in watermelon and their responses to environmental stresses and plant hormones. In this study, we performed a genome-wide identification of ClWRKYs in watermelon and analyzed their classification, chromosome distribution, phylogeny, structure, duplication, conserved motifs, and expression patterns in different tissues. Moreover, we further investigated the expression profiling of ClWRKY genes in response to abiotic stresses and plant hormones to exploit their potential functions in abiotic stress tolerances. Our study identified a subset of potential candidate ClWRKYs which can be utilized for enhancement of stress tolerance in Cucurbitaceae through genetic manipulation and rational breeding.
Materials and methods
Identification and annotation of WRKY genes in watermelon
To genome-wide identify WRKY genes in watermelon genome, both BLAST and Hidden Markov Model (HMM) methods were used in this study. Firstly, 22 and 102 WRKY proteins identified from Arabidopsis (https://www.arabidopsis.org/) and rice (http://rice.plantbiology.msu.edu/) were used as query sequences to search against the watermelon protein database (Version1, http://www.icugi.org) using BLASTP program with default settings. In addition, the HMM profile of the WRKY DNA-binding domain (Pfam: PF03106) downloaded from Pfam database (http://pfam.xfam.org/) was also exploited for identification of WRKY genes from watermelon using HMMER3.0 with E-value setting to 1e-2 [31]. Then, all putative non-redundant candidates were further subjected to identify partial or intact WRKY homologs in watermelon genome using TBLASTN methods (E-value setting to 1e-10). After parsing the BLAST files with in-house perl scripts, the new homologs were validated using non-redundant protein database from NCBI, and only sequences with best hit of WRKY protein were considered as candidate genes. Finally, all non-redundant putative WRKY genes were examined by the presence of WRKY domains using Conserved Domain Database (http://www.ncbi.nlm.nih.gov/cdd/), Pfam and ScanProsite (http://prosite.expasy.org/scanprosite/).
Using the software JoinMap 4.0 (https://www.kyazma.nl/index.php/mc.JoinMap/), the distribution of watermelon WRKY genes were constructed based on their chromosomal locations. Additionally, the molecular weight (MW), Theoretical isoelectric point (pI), instability index, aliphatic index, Grand average of hydropathicity (GRAVY) of watermelon WRKY proteins were predicted via the ProtParam tool from ExPASy (http://web.expasy.org/protparam/). An advanced protein subcellular localization prediction tool WoLF PSORT (https://wolfpsort.hgc.jp/) was used to predict the subcellular localization.
Multiple sequence alignment, classification, and phylogenetic analysis
The protein sequences of ClWRKY genes obtained from watermelon, as well as 7 AtWRKY genes (AtWRKY6, AtWRKY11, AtWRKY22, AtWRKY25, AtWRKY56, AtWRKY60 and AtWRKY66), were aligned using software MUSCLE [32], and visually edited by GENEDOC to analyze the conserved WRKY core domain (60 amino acid). A further multiple sequence alignment of 184 complete protein sequences (listed in S1 Table) including 57 ClWRKY genes from watermelon, 72 AtWRKY from Arabidopsis and 55 CsWRKY from cucumber, was performed using MUSCULE. Based on the alignment, a neighbor-joining phylogenetic tree was constructed using MEGA 7.0 with 1000 bootstrap value and Jones-Taylor-Thornton (+ G) method [33]. An online software iTOL was applied to beautify the phylogenetic tree (http://itol.embl.de/).
Gene structure analysis and identification of motifs
The exon-intron organization of the watermelon WRKY genes were generated by comparing their coding sequences (CDS) with their respective full-length sequences (http://cucurbitgenomics.org/) using the online program Gene Structure Display Server (GSDS: http://gsds.cbi.pku.edu.cn) [34]. The conserved motifs of ClWRKY proteins were analyzed online using Multiple Expectation Maximization for Motif Elicitation (MEME) with default parameters (http://meme-suite.org/tools/meme).
Gene duplication and synteny analysis
Duplication pattern and synteny analysis were performed following the procedures described previously [35]. All watermelon WRKY protein sequences were searched against themselves and proteins of Arabidopsis respectively, using BLASTp program with E-value setting to 1e-10 and output format as tabular (-m 8). Then, the destination tabular file, as well as the GFF files of watermelon and Arabidopsis genomes, were inputted into software MCScanX to analyze duplication types and syntenic relationship [36], and visualized using CIRCOS (http://circos.ca/).
Plant material and treatments
The seeds of watermelon inbred line ‘Y34’, a typical East Asia ecotype were provided by the Cucurbits Germplasm Resource Research Group at Northwest A&F University, Yangling, Shaanxi, China. For tissue-specific analysis, germinated seeds were directly sown in the experimental base at Northwest A&F University, Yangling, Shaanxi, China (34°20′N, 108°24′E), and the roots, stems, leaves, tendrils, fruit, male and female flowers were sampled separately during the fruit maturation period. For other treatments, germinated seeds were sown in plastic pots (8 cm × 7 cm × 7 cm) filled with commercial peat-based compost (Shaanxi Yufeng Seed Industry Co., Ltd., Yangling, China). The seedlings were grown under spring time natural light in a greenhouse at Northwest A&F University, where the temperature was 28–35°C /16–20°C (day/night). All plants were uniformly watered daily and nourished weekly with 1/2 strength Hoagland’s solution. Seedlings at the four-week stage were used for the following treatments.
Hormone treatments were performed by spraying leaves with 100 μM ABA [28], 1 mM SA [37], 100 μM methyljasmonate (MeJA), and 10 mM ethephon (ETH) [38], while leaves sprayed with distilled water served as control. Leaves were collected at 0.5, 1, 6, 12, 24, and 48 hours after treatments.
The salinity stress treatment was carried out by irrigating plants with 300 mM NaCl solution (80 mL per plant) in the pots [39], followed by sampling leaves at 6, 24, 48, 72, 96, and 120 hours after treatment. Similarly, plants irrigated with distilled water were used as control. For cold treatment, plants were kept in a growth chamber at 4°C under a light intensity of 300 mmol•m–2•s–1 PPFD [40], then leaves were sampled at 1, 3, 6, 12, 24, and 48 hours after the commencement of cold treatment, whereas seedlings kept at 27±1°C under the same light condition were used as control. The drought stress treatment was accomplished creating a natural drought condition [41], and the control plants were well-watered to 70 ± 5% field capacity based on weighing. Then the drought-stressed and control leaves were sampled at 24, 48, 96, and 192 hours after treatment. In our study, at each time point of each treatment, the topmost second fully expanded leaves from four plants were pooled together in each biological sample, and three biological replicates were used in all treatments. Harvested samples were rapidly frozen in liquid nitrogen and stored at -80°C for further analysis.
RNA isolation and semi-quantitative reverse-transcription PCR analysis
Total RNA of sampled leaves was extracted using the RNASimple Total RNA Kit (DP432, TIANGEN, China). The integrity and quality of RNA were analyzed via 1.0% agar gel electrophoresis and the NanoDrop 2000C Spectrophotometer (Thermo Fisher Scientific, USA). Approximately 1 μg of total RNA was used for the synthesis of first strand of cDNA by the FastKing RT Kit with gDNase (KR116, TIANGEN, China). Gene-specific primers for the ClWRKY genes were designed using Primer Premier 6.0 (S2 Table). Semi-quantitative reverse-transcription (RT) PCR (LifeECO-TC96, BIOER, China) was done following the PCR procedures: initial denaturation at 94°C for 90 s, followed by 40 cycles of denaturation at 94°C for 30 s, annealing at 58 ± 5°C for 30 s, extension at 72°C for 30 s, and a final extension at 72°C for 5 min. The amplification was done in a 20 μl reaction volume, which contained 10.0 μl 2×Taq Master Mix (E005, novoprotein, China), 0.6 μl of each primer (10 μM), 1.0 μl cDNA template, and 7.8 μl ddH2O. Meanwhile, a housekeeping gene β-actin gene (Cla007792) was used as internal control [42]. All PCR products were measured on a 2.0% agarose gels and imaged under UV light (ChampGel 6000, SAGECREATION, China) for gene expression analysis.
Real-time quantitative PCR
The quantitative RT-PCR was conducted on a LightCycler® 96 real time-PCR machine (Roche, Switzerland) using SYBR® Premix Ex Taq™ II (TaKaRa Biotechnology, Dalian, China). The amplification was done in a 20 μl reaction volume, which contained 10.0 μl SYBR Green Premix, 0.8 μl of each primer (10 μM), 1.0 μl cDNA template (80 ng/μl), and 7.4 μl ddH2O. The PCR parameters were pre-denaturing at 95°C for 30 s, 40 cycles at 95°C for 5 s, and 60°C for 30 s. Melt-curve analyses were carried out using a program with 95°C for 15 s and then a constant growth from 60°C to 95°C with temperature increasing steps of 0.3°C/s. The gene-specific primers were same as those used for semi-quantitative RT-PCR (S2 Table). The watermelon β-actin gene (Cla007792) was used as an internal reference gene [42]. Each treatment was repeated using three technical replicates. All data from real-time quantitative PCR was calculated for relative expressions following the 2-ΔΔCt method as described by Livak and Schmittgen [43]. The relative expressions values were log2 transformed and were displayed in heat map using MeV 4.8.1(http://www.mybiosoftware.com).
Results
Identification and characterization of WRKY genes
As shown in Table 1, a total of 63 putative ClWRKY genes, including 57 full-length WRKY genes and 6 WRKY partial homologs, were finally identified in watermelon by HMM (PF03106) and TBLASTN search methods. All of these ClWRKY genes could be mapped on the chromosomes from chromosome 1 to 11 and were renamed from ClWRKY1 to ClWRKY63 based on their order on the chromosomes (Table 1; S1 Fig). The coding sequences (CDS) of 57 full-length ClWRKYs ranges from 366 to 2295 bp and the molecular weight (WM) of them varies from 14049.65 to 82969.81 Da. According to the isoelectric point (pI), 32 ClWRKYs were acidic proteins with pI value less than 7.0, and the remaining 25 proteins were basic proteins. According to the instability index, most of ClWRKY proteins, with the value of instability index higher than 40.0, were instability, except ClWRKY13 and ClWRKY29. Additionally, the WoLF PSORT prediction showed that 53 ClWRKY proteins were localized in nucleus, suggesting ClWRKY proteins play regulatory roles mainly in cell nucleus.
Multiple sequence alignment and phylogenetic analysis
The conserved heptapeptide of WRKYGQK is the most obvious structural feature of WRKY proteins, which can interact with the W box to activate target genes [2]. The WRKY domains spanning approximate 60 amino acids were analyzed using multiple sequence alignment (Fig 1). Heptapeptide WRKYGQK in most ClWRKY proteins was highly conserved. However, that in ClWRKY1 and ClWRKY47 mutated into KRQVEVQ and WRKYGKK, respectively, and that in ClWRKY2, ClWRKY5, ClWRKY11 and ClWRKY46 was missed. Additionally, identified zinc-finger motifs in some proteins encoded by ClWRKY3, ClWRKY15, ClWRKY24, and ClWRKY44 were missed.
Alignment was accomplished using MUSCLE. ‘N’ and ‘C’ indicate the N-terminal and C-terminal WRKY domain of a specific WRKY protein, respectively. The amino acids forming the zinc-finger motif are highlighted in blue, the conserved WRKY amino acid domains is highlighted in green.
To analyze the evolutionary relationships, a total of 184 WRKY genes, including 57 from watermelon, 55 from cucumber, and 72 from Arabidopsis, were used to generate a phylogenetic tree (Fig 2). Based on the WRKY domains and the specific zinc-finger motifs, 57 ClWRKYs were classified into three groups (I-III) with 11 ClWRKYs in group I, 39 in group II, and 7 in group III. The ClWRKYs in Group II were further divided into five subgroups (IIa-IIe) with the most genes in Group IIc. Obviously, proteins in group I contained two WRKY domains located at both the N-terminus and C-terminus and the zinc finger motif of C2H2 type at N-terminus and C-terminus was C-X4-C22-H-X-H and C-X4-C23-H-X-H, respectively (Fig 1). By contrast group I, group II and group III genes had only one WRKY domain. Proteins in group IIa, IIb, IId and IIe contained a zinc finger motif of C-X5-C23-H-X-H, whereas those in group IIc contained a zinc finger motif of C-X4-C23-H-X-H at C-terminus, except ClWRKY1. Group III proteins contained a C2HC zinc-finger motif of C-X7-C-X23-H-X-C at C-terminus. In addition, sequence comparisons and phylogenetic analyses showed that WRKY proteins from three species appeared scattered across the branches of the evolutionary tree, implying that they experienced duplications after the lineages diverged. Meanwhile, a total of 42 WRKY genes from cucumber and watermelon were clustered as 21 pairs (Fig 2), indicating that they were the orthologous WRKY domains from the same lineage.
The domains clustered into three major groups I, II, III, and five subgroups (a, b, c, d, and e) in group II.
Gene structure and conserved motifs analysis
The exon-intron analysis was performed to obtain a better insight into the structure of ClWRKY genes, which exhibited relatively smaller variation in numbers of exons and introns. As shown in Fig 3, 57 ClWRKY genes had two to six exons. Among them, 27 ClWRKYs had three exons, followed by eleven ClWRKYs with four exons, eight ClWRKYs with two exons, eight ClWRKYs with five exons, and three ClWRKYs with six exons. These divergences suggested that both exon gain and loss was occurred during the evolution of the WRKY gene family. ClWRKY genes in the same group usually seemed to have similar exon-intron structures. For instance, six genes from seven members in Group III had three exons. In comparison to ClWRKYs in group II and group III, those in group I had more exons, ranging from four to six. These findings provided an additional foundation to support the classification of ClWRKYs.
Genes were separated into their respective groups with different colors. Exons were shown using green round-corner rectangle while introns were shown using black solid lines (5′-3′).
We further searched for the conserved motifs in 57 ClWRKY proteins using MEME program (Fig 4). In total, 24 conserved motifs named as motif 1 to motif 24 were identified and the details of the 24 putative motifs were listed in S3 Table. Motif 1 and 2 were found in most of ClWRKY genes. Motifs 1, 3, and 15 contained a WRKYGQK sequence. As expected, most ClWRKY proteins in the same group or subgroup possessed similar motifs, suggesting their functional equivalency. For example, motifs 1, 2, 3, 4, and 9 were present in group I proteins, which contained two WRKY domains, whereas group III proteins possessed motifs 1, 2, 8, and 17.
Conserved motifs were named as motif 1 to motif 24, and different motif was shown as colored boxes with their names in the center of the boxes. The colored boxes were ordered manually according to the results of the MEME analysis. The length of each box in the figure does not represent the actual motif size.
Gene duplication and synteny analysis
Currently, we evaluated the gene duplication events of ClWRKY genes using MCScanX program. Ninety-four syntenic relations of ClWRKYs were identified as duplication events in watermelon genome (Fig 5; S4 Table), and 45 ClWRKY genes were located within syntenic blocks on all watermelon chromosomes. Chromosome 1, 5 and 10 had more duplication regions and that could partly explain the larger numbers of ClWRKY genes located on these three chromosomes. Gene duplication events are defined as either tandem duplications, with two or more genes located on the same chromosome, or segmental duplications, with duplicated genes present on different chromosomes [44]. There were 11 ClWRKY genes clustered into 6 tandem duplication event regions on watermelon chromosome 1 (ClWRKY4/ClWRKY6 and ClWRKY7/ClWRKY8), 5 (ClWRKY23/ClWRKY27 and ClWRKY27/ClWRKY30), 7 (ClWRKY40/ClWRKY42), and 10 (ClWRKY59/ClWRKY60). The other 88 syntenic relations of ClWRKY genes were confirmed as segmental duplications, suggesting that most ClWRKY genes were possibly generated by gene segmental duplication.
Chromosomes 1–11 were shown with different colors and in a circular form. Colored curves indicated the details of syntenic regions in watermelon genome.
Arabidopsis was widely used as a model system for plant WRKY TFs research [45]. In order to further explore evolutionary and functionality connections between watermelon and Arabidopsis WRKY genes, a synteny analysis was performed. A total of 103 pairs of syntenic relations were identified, including 51 AtWRKY genes and 45 ClWRKY genes (Fig 6; S5 Table). Out of these genes, 13 AtWRKY genes and 18 ClWRKY genes were found to be associated with at least three synteny events, and three ClWRKY genes (ClWRKY8, ClWRKY18 and ClWRKY23) were involved in six synteny events. A lot of synteny events indicate that numerous WRKY genes existed before the divergence of the Arabidopsis and watermelon.
The chromosomes of watermelon and Arabidopsis are depicted as a circle. Colored curves denote the details of syntenic regions between watermelon and Arabidopsis WRKY genes.
Expression profiles of the ClWRKY genes in different tissues
By means of semi-quantitative observation, we analyzed the expression profiles of 57 full-length ClWRKY genes in seven different tissues including roots, stems, leaves, tendrils, fruit, male flowers, and female flowers under normal growth conditions. Then, the gene-specific primers of 52 ClWRKYs were successfully found in our study (S2 Table). The results showed that 52 ClWRKYs genes were detected in at least one of the seven tested tissues (Fig 7). Among them, 17 (33%) ClWRKY genes were expressed in all tested tissues. The other genes were detected in only one or several tissues. For instance, ClWRKY37 and ClWRKY42 were found only in roots, whereas ClWRKY15 was preferential accumulation in male flower. Some genes such as ClWRKY61 and ClWRKY56 were not observed in any tested tissue possibly due to their expression in other tissues or too low expression level (below detection limit via semi-quantitative observation).
β-actin gene was used as the internal control. Six amplified bands from left to right for each WRKY gene represent amplified products from R: root; S: stem; L: leaf; T: tendril; FF: female flower; MF: male flower and F: fruit.
Expression patterns of the ClWRKY genes under various abiotic stresses
To investigate the potential roles of ClWRKY genes in response to abiotic stresses, we analyzed their dynamic response after exposure to drought, cold, and salinity stresses using qRT-PCR. ClWRKY genes exhibited different expression patterns in response to different stresses (Fig 8). Drought treatment continuously induced the expression of about half of the detected ClWRKY genes but reduced the expression of four ClWRKY genes including ClWRKY18, ClWRKY23, ClWRKY27 and ClWRKY58. The expression of ClWRKY15, ClWRKY25 and ClWRKY61 transiently increased at 24 h but decreased at 192 h after drought treatment. Additionally, 11 ClWRKYs such as ClWRKY12, ClWRKY34, and ClWRKY41 slightly induced or reduced at the earlier or later period of drought stress. Similarly, cold stress (4°C) continuously up-regulated and down-regulated about half of detected ClWRKYs and four ClWRKY genes (ClWRKY13, ClWRKY32, ClWRKY51 and ClWRKY56), respectively. Several ClWRKYs such as ClWRKY27 showed a transient down-regulation at 1 h but then continuously up-regulated with the advancement of cold stress. Most of ClWRKY genes were up-regulated but only ClWRKY18 were down-regulated by the NaCl treatment. Some ClWRKYs such as ClWRKY58 showed a transient down-regulation at the median or later period of salt stress. Notably, the expressions of ClWRKY14 and ClWRKY60 were up-regulated by all stresses, suggesting that these two genes may play a core role in plant tolerance to diverse abiotic stresses.
The abiotic stresses used for expression patterns are indicated at the top. Scale bars on the top of each heat map represent log2-transformed (Treatment/Control) values, with red as increased expressed level and green as decreased expressed level. (A) Expression of ClWRKY genes under drought stress, and 24, 48, 96, and 192 indicate hours after treatment. (B) Expression of ClWRKY genes under 4°C treatment, and 1, 3, 6, 12, 24, and 48 indicate hours after treatment. (C) Expression of ClWRKY genes under salt stress treatment, and 6, 24, 48, 72, 96, and 120 indicate hours after treatment.
Expression patterns of the ClWRKY genes to hormone treatments
Numerous evidences have indicated that WRKY TFs are involved in signal pathways of various plant hormones such as ABA, MeJA, SA, and ETH [46]. As shown in Fig 9, ABA treatment induced both up- and down-regulation of almost all ClWRKYs at different time points. Most of ClWRKYs were down-regulated or remained unchanged at 0.5 and 1 h but ABA application up-regulated their expression at 12 h and 24 h. Similarly, many of ClWRKY genes were both up-regulated and down-regulated at different periods by MeJA, as well as ABA treatment. Most of ClWRKYs were induced or remained unchanged at 0.5, 6, 12, and 48 h but MeJA treatment reduced their expression at 24 h. Being different with ABA and MeJA, SA application induced continuous up-regulation of 12 ClWRKYs and down-regulation of three ClWRKYs. The other ClWRKYs showed different expression patterns at different time-points after SA treatment. In response to ETH treatment, about a half of ClWRKY genes showed continuous up-expression from 1 to 48 h, with some exceptions showing down-expression at 24 h and 48 h. ETH treatment down-regulated expression of the other ClWRKYs. These results indicate that ClWRKY genes are positively or negatively involved in regulatory pathways of plant hormones and thus play important roles in plant growth, development, and defense against environmental stresses.
Scale bars on the top of each heat map represent log2-transformed (Treatment/Control) values. The hormone treatments including abscisic acid (ABA), methyl jasmonic acid (MeJA), salicylic acid (SA) and ethephon (ETH) are shown as heatmaps (A), (B), (C) and (D), respectively. 0.5, 1, 6, 12, 24 and 48 indicate hours after treatment.
Discussion
Annotation and characterization of WRKY genes in watermelon genome
Due to the important roles of WRKY transcriptional factors in plant growth, development, and response to stresses, a large number of WRKY families have been identified in diverse plant species (S6 Table). However, there is dearth of information about WRKY genes in watermelon. Here, we identified a total of 63 putative ClWRKY genes in watermelon. In addition to 57 full-length ClWRKY genes, 6 ClWRKY partial homologs (ClWRKY2, ClWRKY5, ClWRKY11, ClWRKY43, ClWRKY46 and ClWRKY48) were found using TBLASTN method with in-house Perl scripts. This operation ensured that WRKY genes were complete in watermelon genome, although no particular annotation information was available for these 6 WRKY partial homologs. Moreover, our further analysis revealed the properties (i.e. amino acid length, molecular weight, isoelectric point, and instability) and subcellular location of ClWRKY proteins.
According to the classification of WRKY genes in Arabidopsis [2], 57 full-length ClWRKY genes were also classified into three groups (I-III) and five subgroups (IIa-IIe) of group II based on their conserved WRKY domain and zinc-finger motif. The size of ClWRKYs in each group is similar to that of CsWRKYs in cucumber [47], indicating a similar evolutionary pattern between watermelon and cucumber (Fig 2). However, the size of the ClWRKY gene family (63) is small compared to that of model plants such as Arabidopsis (72) and rice (102). The differences in the number of WRKY genes in group III are the primary cause of the diverse sizes of WRKY gene families (S6 Table). Group III WRKY genes have been described as a newly defined and the most dynamic group with a large number of duplications events [7]. Therefore, group-III WRKY genes may play important roles in plant evolution.
The number of exons in ClWRKY genes varied from two to six (Fig 3), and the exon-intron structural diversification might be caused by the rearrangement and fusions of different chromosome fragments [44, 48]. This finding provided an additional foundation to support the classification of ClWRKYs and a way to find out which group WRKY genes might be of a more ancient origin [8]. Moreover, we should pay attention to the roles of special motif in only one group, such as motif 16 in group IId proteins and motif 17 in group III proteins (Fig 4), which may possess some hitherto uncharacterized roles.
Multiple sequence alignments revealed that WRKYGQK sequence was highly conserved in most of ClWRKY TFs. The WRKYGQK sequence was considered to be important for recognizing and binding to W box elements in the promoter of target genes [3]. Previous studies have reported a number of variants of the WRKYGQK sequence in diverse plant species and proteins with these variants may recognize the other binding elements other than the W box element [7, 49]. In watermelon WRKY genes, we found two variants of the WRKY domain: WRKYGKK in ClWRKY1 and KRQVEVQ in ClWRKY47 (Fig 2). WRKYGKK sequence was the most common variant in many plants and proteins with this sequence instead of WRKYGQK could bind specifically to WK box (TTTTCCAC) [50, 51]. Strikingly, variant KRQVEVQ sequence was found only in watermelon (ClWRKY1). Variations of WRKYGQK motif might change DNA binding specificities of downstream target genes, and thus it would be interesting to validate the biological functions of ClWRKY1 and ClWRKY47. Moreover, deletion events of the zinc-finger motif occurred in four ClWRKY genes (ClWRKY3, ClWRKY15, ClWRKY24 and ClWRKY44) in group IIc. The replacement or deletion of the zinc-finger motif might lead to the evolution and classification of WRKY genes [44, 52]. However, it remains largely unknown whether the deletions of zinc-finger motif influence the function and the expression patterns of WRKY genes.
Expansion and synteny of ClWRKY genes
Gene duplications played a crucial role in genomic rapid expansions and evolution of gene families [53]. A number of evidence pointed that duplication and expansion events happened in plant WRKY genes [44, 54, 55]. Here, 6 tandem duplication event regions and 88 segmental duplications event regions of ClWRKY genes were confirmed in watermelon chromosome (Fig 5; S4 Table), suggesting that low-tandem and high-segmental duplications events existed in ClWRKY genes family. This finding is in agreement with that in Arabidopsis and Populus trichocarpa [52, 54], but incongruent with that in rice [21], which could be due to a large scale artificial selection and the differences of life cycle between rice and watermelon. Interestingly, three ClWRKY genes (ClWRKY23, ClWRKY27 and ClWRKY40) with tandem duplication were belonged to group III genes, implying that a different pattern of duplication may cause smaller size of group III WRKY genes in watermelon.
Moreover, most of ClWRKY genes were found in syntenic genomic regions of Arabidopsis (Fig 6; S5 Table). The large numbers of gene duplication events between watermelon and Arabidopsis will help us to understand the functions of ClWRKY genes. For example, over-expression of AtWRKY57 in rice improves drought and salt tolerance [56]. Moreover, AtWRKY70 is involved in brassinosteroids (BRs)-regulated growth and negatively affects drought responses [57]. Meanwhile, ClWRKY60 and ClWRKY61 were in the synteny region with these well-known AtWRKY genes, predicting a similar functional mechanism of ClWRKY60 and ClWRKY61 in drought resistance in watermelon. Nevertheless, gene functional study is required to better predict their roles.
Possible roles of ClWRKY genes in normal and stress conditions
Results from numerous studies demonstrate that WRKY transcription factors play very critical role in different tissues to regulate plant growth and developmental processes [3]. For instance, virus-induced silencing of GmWRKY58 and GmWRKY76 in soybean causes severe stunted growth with reduced leaf size and plant stature [58], and overexpression of the OsWRKY31 could reduce lateral root formation and elongation [10]. In our study, ClWRKY13, ClWRKY31, ClWRKY51 and ClWRKY63 showed higher expression levels in all tested tissues (Fig 7). Among them, ClWRKY13 and ClWRKY63 were orthologous genes of CsWRKY49 and CsWRKY37, respectively, implying that these genes play key roles in the whole-plant growth and development [21, 47]. Furthermore, some ClWRKY genes were specifically expressed in a certain tested tissue. As shown in Fig 7, ClWRKY15 were preferentially expressed on male flower, suggesting that ClWRKY15 might play important roles during development of male reproductive organs. In addition, ClWRKY genes with low expression level in all tested tissues might be expressed specifically in other tissues such as seeds, or could be induced under environment stimuli. For example, ClWRKY56 and ClWRKY61 were not detected in leaves under normal condition, but they were induced by abiotic stresses (Fig 7), suggesting the involvement of these genes in stress signaling.
Increasing evidence show that WRKY proteins in various plant species are involved in the response plants to various abiotic stresses such as drought, cold, and salt [16, 59]. In Arabidopsis, rice, and cucumber, at least 20, 54, and 23 WRKY genes were identified in response to diverse abiotic stress, respectively [17, 21, 47]. The responses of ClWRKYs to abiotic stress and plant hormones treatments can provide useful clues for dissecting the potential roles of WRKY genes in watermelon. In this study, we found that most of ClWRKYs positively or negatively responded to drought, cold, and salt stresses, and their responses altered with the degree of stresses. These results provided a useful reference for functional verification of ClWRKYs under environmental stresses. Additionally, the expression patterns of ClWRKYs in watermelon responses to abiotic stresses differed greatly from those in other plant species such as cucumber and pear [47, 60], suggesting that there were different gene duplication and evolution ways among different plant species.
Orthologous genes are generally supposed to retain equivalent functions in different species and to share other key properties [60]. The comparative analysis of ClWRKY genes with their homologous genes in other plant species helped to predict the potential functions of WRKY proteins in watermelon. In cucumber, CsWRKY46 can be induced by various stresses and its overexpression conferred cold tolerance to transgenic plants by positively regulating signaling pathway [47, 61]. As its orthologous genes, ClWRKY8, ClWRKY34 and ClWRKY53 also showed significant up-regulation under salt, cold, and drought stress, respectively (Fig 8), these genes may play similar roles with CsWRKY46 in stress response. Ding et al. [62] demonstrated that AtWRKY46 played dual roles in regulating plant responses to drought and salt stresses. Its orthologous gene ClWRKY23 also was found to be up-regulated under drought and salt stresses. AtWRKY25 in Arabidopsis has been known to respond to both heat and salt treatments [63]. Similarly, its orthologous gene ClWRKY60 is obviously and continuously induced by multiple abiotic stresses. These results imply that a single WRKY gene may play various regulatory roles in response to stresses. In addition, AtWRKY70 and AtWRKY54 co-operate as negative regulators for stomatal closure and thus regulate osmotic stress tolerance in Arabidopsis [20]. The negative responses of their orthologous genes ClWRKY41 and ClWRKY61 at the end of drought treatment imply they can play negative regulatory roles at the later period of drought.
Given that plant hormones such as ABA, SA, JA, and ETH, play critical roles in regulating plant growth, development, and defense against various abiotic and biotic stresses [17, 64, 65], a number of WRKY genes have been demonstrated to be involved in diverse plant hormone signal pathways [20, 23]. Ding et al. [66] revealed that the expression of AtWRKY46 was repressed by ABA signal, but induced by an ABA-independent signal under osmotic and salt stress, as well as AtWRKY54, AtWRKY70, and CsWRKY46 [20, 61]. As homologous of these well-known WRKY genes, ClWRKY60, ClWRKY23, ClWRKY41 and ClWRKY61 expressions in watermelon were up-regulated by drought stress (Fig 8), but were down-regulated by ABA at 0.5 or 1 h after treatment (Fig 9). Thus, these four ClWRKY genes may regulate watermelon response to drought stress via interacting with ABA signaling. In addition, Cho et al. [67] and Yang et al. [68] found that ClWRKY70 (same as ClWRKY41 in this study) and ClWRKY1 (same as ClWRKY17 in this study) play a positive regulatory role in plant resistance against pathogen attack. In our study, ClWRKY41 and ClWRKY17 were significantly up-regulated by SA treatment, implying that these two genes were involved in SA-mediated signaling pathways in plant defense responses. These results indicate that the regulatory mechanism of WRKY proteins under abiotic stresses is complex and the functional dissection of WRKY genes in signaling pathways and stress responses will be an important research topic for the future.
Conclusions
In this study, we identified watermelon WRKY family genes and analyzed their expression patterns for the first time. A total of 63 putative ClWRKY genes in watermelon were obtained using comprehensive computational approaches. All 63 ClWRKY genes located on 11 chromosomes were classified into three major groups (I-III) and five subgroups (IIa-IIe) in group II. ClWRKYs may play multiple regulatory roles based on their varied structures with conserved or varied WRKY domain and different motifs. The expression of ClWRKYs in different tissues indicated that they were involved in various tissue growth and development. Furthermore, the diverse responses of ClWRKYs to abiotic stresses suggested that they positively or negatively participated in plant tolerance against drought, salt, or cold stress. Altered expression patterns of ClWRKYs by phytohormones such as, ABA, SA, MeJA, and ETH, implied the existence of complex crosstalks between ClWRKYs and plant hormone signals in regulating plant physiological and biological processes. Therefore, our findings provide valuable clues for further research on the function and regulatory mechanisms of ClWRKY TFs in watermelon growth, development, and adaption to environmental stresses.
Supporting information
S1 Table. Full-length protein sequence of WRKY genes from watermelon, Arabidopsis, and cucumber.
https://doi.org/10.1371/journal.pone.0191308.s001
(XLSX)
S2 Table. The primers of WRKY genes in watermelon.
https://doi.org/10.1371/journal.pone.0191308.s002
(XLSX)
S3 Table. The details of the 24 putative motifs of watermelon WRKY genes.
https://doi.org/10.1371/journal.pone.0191308.s003
(DOCX)
S4 Table. The synteny regions between watermelon WRKY genes.
https://doi.org/10.1371/journal.pone.0191308.s004
(XLSX)
S5 Table. The synteny regions between watermelon and Arabidopsis WRKY genes.
https://doi.org/10.1371/journal.pone.0191308.s005
(XLSX)
S6 Table. Number of WRKY TF gene family members present in major crop plants and horticultural plants.
https://doi.org/10.1371/journal.pone.0191308.s006
(DOCX)
S7 Table. The relative expression of watermelon WRKY genes via qRT-PCR in response to various abiotic stresses and hormone treatments.
https://doi.org/10.1371/journal.pone.0191308.s007
(XLSX)
S1 Fig. Genetic map position on watermelon chromosomes of WRKY gene family.
The numbers indicate the start site of WRKY genes located on chromosomes.
https://doi.org/10.1371/journal.pone.0191308.s008
(TIF)
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