- Research article
- Open Access
Characterization and co-expression analysis of WRKY orthologs involved in responses to multiple abiotic stresses in Pak-choi (Brassica campestris ssp. chinensis)
© Tang et al.; licensee BioMed Central Ltd. 2013
Received: 6 August 2013
Accepted: 22 November 2013
Published: 25 November 2013
The WRKY transcription factor is an important member of the stress-related transcription factors, which mediate diverse abiotic stresses in many plants. However, up until now, the number of WRKY members, and the regulatory mechanisms involved in abiotic stress responses in Pak-choi (Brassica campestris ssp. chinensis), remained unknown.
We isolated and identified 56 full-length WRKY cDNAs from a Pak-choi stress-induced cDNA library. The 56 putative BcWRKY proteins were divided into three groups based on structural and phylogenetic analyses. A subcellular localization prediction indicated that the putative BcWRKY proteins were enriched in the nuclear region. Experiments involving BcWRKY25 and BcWRKY40 confirmed the prediction. A total of 22 BcWRKYs were differentially expressed in response to at least one stress condition (abscisic acid, cold, salinity, heat, or osmosis) tested on Pak-choi leaves, and a co-expression analysis indicated stress-inducible BcWRKYs co-regulated multiple abiotic stresses. BcWRKY33, BcWRKY40, BcWRKY53, and BcWRKY70 acted as key regulators and played dominant roles within co-regulatory networks of stress-inducible BcWRKYs.
We first isolated and characterized the 56 stress-inducible WRKY transcription factor family members. A total of 22 stress-inducible BcWRKYs found in leaves can co-regulate multiple environmental stresses by integrating the potential mutual interactions of WRKYs in Pak-choi. This information will be valuable when exploring the molecular mechanisms of WRKYs in response to abiotic stresses in plants.
To overcome environmental stresses, plants have developed the ability to perceive and respond to these diverse external signals using specialized physiological and biochemical strategies [1, 2]. Plant stress responses are generally controlled by a network of specialized genes that are intricately regulated by specific transcription factors (TFs) . The WRKY TFs are important members of the stress-related TFs involved in regulating the plant’s environmental stress responses [4–6]. The WRKY TF family was named based on the presence of a 60 amino acid (aa) WRKY domain that is defined by a highly conserved WRKYGQK heptapeptide at the N-terminus and a zinc-finger-like motif at the C-terminus. WRKY proteins can be classified into three groups (I, II, and III) based on the number of WRKY domains and the pattern of the zinc-finger motif [5, 7].
The WRKY TF family is a large conserved family of TFs that has been reported in many plants [8–15]. WRKY TFs have been found to be responsive to various abiotic stresses, including salinity, drought, cold, heat, and abscisic acid (ABA) signaling [16–20]. For instance, the NaCl-inducible AtWRKY25 and AtWRKY33 mediate abiotic stresses . AtWRKY63 is involved in plant responses to ABA and drought tolerance , and AtWRKY34 mediates the cold sensitivity of mature pollen in Arabidopsis. WRKY40, WRKY18, and WRKY60 interact with ABAR and negatively regulate ABA signaling . Alleles of OsWRKY45-1 and OsWRKY45-2 play different roles in ABA signaling and salt stress tolerance in rice . WRKY8 antagonistically interacts with VQ9 to modulate salinity stress tolerance . Additionally, BcWRKY46, a novel cold-inducible gene from Pak-choi (B. campestris ssp. chinensis, synonym of B. rapa ssp. chinensis) enhances the cold, salt and dehydration stress tolerance in transgenic tobacco .
Because of the functional complexity of the WRKY genes involved in environmental stresses, many approaches have been used to explore the unknown mechanisms of the stress response processes. Previous studies have demonstrated the power of co-expression analysis as a candidate discovery tool [27–29], which encouraged us to explore this approach for the identification of genes putatively involved in these interesting biological processes. Additionally, a co-expression analysis of OsWRKYs under biotic and abiotic stress conditions has been reported .
Pak-choi is an important Brassica crop with exceptional cold resistance , and its nearest genetic relative that has been sequenced is Chinese cabbage (B. rapa ssp. pekinensis) , which provides an effective model for Pak-choi research. Although WRKYs have been reported to mediate various stresses, the number of WRKY members in Pak-choi and their roles in response to abiotic stress tolerance were still unknown. Here, we cloned and identified 56 stress-inducible WRKY orthologs from Pak-choi, and we systematically investigated their organization, subcellular localization, and expression patterns under multiple abiotic stresses. In addition, we simultaneously measured co-expression of the stress-inducible WRKY orthologs in Pak-choi and Arabidopsis thaliana. We subsequently established a co-regulatory network of stress-inducible BcWRKYs to multiple abiotic stresses, and indicated the possible interactions of stress-inducible BcWRKY gene pairs.
Cloning stress-inducible BcWRKY genes from Pak-choi
Identification of stress-inducible WRKY genes in Pak-choi
Phylogenetic analysis and identification of conserved motifs
Motif sequences of 56 BcWRKY proteins identified by MEME tools
Known motif description
Nuclear location signal
Alignment and comparison of WRKY domains
By comparing the 67 WRKY domains, a phylogenetic tree with five clades was constructed (Figure 2). In terms of the eight WRKY domain patterns, the ICT group was placed in clade I, and the next branch, clade II, consisted of group IIc. This was considered as an intermediate between clades I and III, which involved groups ICT and INT. While clade III, including the INT group, was placed as an original node, the remaining 31 domains were clustered into clade IV (groups IIa and IIb) and clade V (IId, IIe, and III). These results illustrated the evolution of Pak-choi WRKY domains from group I to group II or III (Figure 2). For example, BcWRKY51 and BcWRKY59, belonged to group IIc, but they were clustered into the INT group in the phylogenetic tree (Figure 2), and BcWRKY32 protein belonged to group I, containing two WRKY domains, but clustered into the IIc group in the phylogenetic tree (Figure 1). A similar evolutionary pattern for WRKY domains has been reported in Arabidopsis and rice .
Subcellular localization analysis of BcWRKYs
Expression patterns of BcWRKYs under multiple abiotic stresses
Co-regulatory networks of BcWRKYs in response to multiple abiotic stresses
To validate the co-regulatory relationships of the BcWRKY genes, we constructed an evident interaction co-regulatory network of WRKY orthologs through the STRING 9.1 database based on the stress-inducible BcWRKY orthologs in Arabidopsis (Additional file 4: Figure S2). Among the 11 co-regulatory WRKY members, each of them existed in at least two mutual relationships with others in the given datasets (Databases, Text-mining, Homology, Experiments, Neighborhood, Co-occurrence, and Co-expression). Those were further verified, and they supported the co-regulatory networks of stress-inducible BcWRKYs in which WRKY33, 40, 53 and 70 represented central nodes.
This study reported the isolation and identification of 56 stress-inducible BcWRKY genes (Table 1) using a homologous gene cloning method from a stress-induced Pak-choi cDNA library. We also systematically surveyed the structure, phylogeny, and conserved motifs of the BcWRKYs and measured the putative protein localization. In addition, a co-expression analysis of BcWRKYs was performed to explore the co-regulatory information of WRKY TFs. Based on a sequence alignment of the BcWRKY domains (Additional file 2: Figure S1), we clearly found phenomena similar to those previously reported . This indicated that possessing different numbers of WRKY domains and zinc finger motifs, and structural variations of the WRKY domain, may produce some novel WRKY members (Additional file 2: Figure S1). For example, the BcWRKY32 protein contains two of the same type of WRKY domains, belonging to Group I; however, in a phylogenetic analysis it can be clustered together with Group IIc members, while BcWRKY59 with WRKY domain features of Group IIc was clustered into a clade with Group IId members because of the absence of some motifs (Figure 1). These results also support the belief that group I WRKYs may represent the ancestral form of the WRKY family . Additionally, the conservation of WRKY domains implies a conserved function for WRKY TFs . For example, the subcellular localization of BcWRKY25 and BcWRKY40 proteins was in the nucleus, which was appropriate for TFs, thus supporting their classification as functional TFs .
Although the mechanisms of the WRKYs’ responses to multiple abiotic stresses needs further investigation, the co-expression analysis, which has the ability to measure large numbers of gene expressions, provides a powerful tool for identifying groups of genes and discovering novel regulators involved in the signal transport of plant stress responses. Previous studies have performed co-expression analyses [29, 30, 36], and found many unknown relationships and novel genes encoding proteins involved in similar expression patterns under different conditions. The co-expression analysis of Arabidopsis and Pak-choi WRKY orthologs (Figure 5 and Additional file 4: Figure S2) indicated co-regulatory relationships and key regulators of 22 stress-inducible BcWRKYs in response to multiple abiotic stresses, and it further indicated the important roles of the WRKY TF mutual interactions to mediate complex biological processes . These findings will help in identifying and understanding more interactive relationships among the WRKYs and will elucidate more co-regulatory relationships for WRKYs under multiple abiotic stresses.
This study isolated and characterized 56 Pak-choi stress-inducible WRKY genes, indicated that 22 BcWRKY genes co-regulated multiple abiotic stress responses in Pak-choi leaves, and established a co-regulatory network of stress-inducible BcWRKYs. The co-regulatory network showed that WRKY33, 40, 53 and 70 were central regulators and had potentially interactive relationships. This study also revealed a method of measuring the common and distinct functions of stress-inducible BcWRKYs among multiple abiotic stress responses, which may aid in exploring the molecular mechanisms of WRKYs in response to abiotic stresses in plants.
Plant materials, growth conditions and stress treatments
Pak-choi (B. campestris ssp. chinensis cv. suzhonqing) was used for all experiments. Seedlings were soaked in distilled water for 0.5 h, and then germinated in plastic Petri dishes containing filter paper saturated with distilled water in darkness at 22°C for 2 days. Seedlings were then transferred to 4 L hydroponic containers containing continuously aerated 1/2 Murashige and Skoog (MS) liquid solution (pH 5.8, without agar and sugar). The 1/2 MS liquid solution was changed once every 3 days. Three-week-old seedlings were transferred to new 1/2 MS liquid solution (pH 5.8, without agar and sugar) for multiple stress treatments under a continuous time course (0, 1, 6, 12, 24, and 48 h). For ABA, salt and osmotic treatments, seedlings were exposed to 1/2 MS solution (pH 5.8) containing 100 μM ABA, 200 mM NaCl and 15% (w/v) polyethylene glycol (PEG), respectively. For cold and heat treatments, seedlings were exposed to the 4 and 38°C conditions in 1/2 MS solution (pH 5.8), respectively. All seedlings were placed under the same growth conditions, except for the different treatment factors, and exposed to 1/2 MS solution at 22°C as controls. The seedlings were harvested under a continuous time courses (0, 1, 6, 12, 24, and 48 h) in three biological replicates for RNA preparation.
Cloning and identification of the BcWRKY members in Pak-choi
Total RNA was extracted from Pak-choi roots, stems, and leaves under multiple abiotic stress conditions using the RNAeasy mini kit (Tiangen, Beijing, China). A mixture of total RNA (1 μg) was used for first-strand cDNA synthesis using a superscript II kit (Takara, Dalian, China) following the manufacturer’s instructions to construct a stress-induced Pak-choi cDNA library. To clone BcWRKY genes, we first designed degenerate primers (5′-YTTYTGNCCRTAYTTNCKCCA-3′, Y = C/T, R = A/G, K = G/T, N = A/G/C/T) and 5′-Oligo(dT)20MN-3′(M = A/G/C, N = A/G/C/T) to amplify the conserved regions of the WRKY orthologs based on sequence information from the A. thaliana WRKY gene family in TAIR10 (http://arabidopsis.org/index.jsp) and the Chinese cabbage chiifu genome in BRAD (http://brassicadb.org/brad/). Based on the results of sequenced polymerase chain reaction (PCR) products from the conserved region of each of the WRKY orthologs and the full length sequences of Chinese cabbage WRKY orthologs (data not shown), we designed gene-specific primers (Additional file 1: Table S1) and performed 5′-and 3′-RACE (Smart RACE cDNA amplification kit; Clontech, Mountain View, CA) to amplify the full-length cDNA sequences of BcWRKYs in the stress-induced Pak-choi cDNA library. The 56 open reading frames (ORFs) from the stress-inducible BcWRKY cDNA sequences were amplified by reverse transcription-polymerase chain reaction (RT-PCR) using gene-specific primers (Additional file 1: Table S1). PCR reactions included a pre-incubation at 94°C for 5 min, followed by 30 cycles of denaturation at 94°C for 30 s, annealing at 55–65°C for 2 min, and extension at 72°C for 10 min. The amplification fragments were cloned in to PMD-19T (Takara). The gene ORF size was confirmed and sequenced using the ABI3730 sequencer (Applied Biosystems, Foster City, CA).
Multiple sequences alignments and phylogenetic analyses
The amino acid sequence alignments of putative BcWRKYs were performed using ClustalW implemented in the MEGA 5 software  with the default settings. They were visualized and manually modified using Jalview 2.7 . Phylogenetic trees of BcWRKY proteins and WRKY domains were built using the maximum likelihood method in MEGA 5. The confidence level of the monophyletic group was estimated using a bootstrap analysis of 1000 replicates.
Identification of conserved motifs
The 56 putative BcWRKY protein sequences used for the phylogenetic analysis were detected by MEME  to analyze possible conserved motifs using the default parameters, except that the maximum number of motifs to identify was defined as eight and the maximum width was set to 200.
Nuclear localization analysis
A subcellular localization analysis of deduced BcWRKY proteins was performed by bioinformatics predictions and experimental approaches. NLSs were detected using NLStradamus , and nuclear protein scores were calculated separately using WOLF PSORT  and NucPred  with the default settings. Meanwhile, two expression vectors were constructed (Figure 3B) to investigate the subcellular localizations of BcWRKY TFs using a transient expression system in onion epidermal cells. The full-length coding sequences of BcWRKY25 and BcWRKY40 were amplified using Gateway-specific primers (Additional file 5: Table S2) cloned into an entry vector, and then subcloned into pEarleyGate101 by Gateway technology (Invitrogen, Carlsbad, CA). The yellow fluorescent marker protein (YFP) was fused to BcWRKY25 and BcWRKY40. Gold particles with a diameter of 1 μm coated with 35S:BcW25-YFP, 35S:BcW40-YFP, and 35S:YFP (Figure 3B) were introduced into onion epidermal cells using particle bombardment (PDS-100/He particle delivery system; Bio-Rad, Hercules, CA). After incubation at 22°C for at least 12 h under darkness, fluorescence and bright-light images were observed by laser scanning confocal microscopy (Leica, TCS SP2, Wetzlar, Germany).
RNA isolation and quantitative real-time PCR (qPCR)
Leaf samples were obtained from control and multiple abiotic stress-treated plants for total RNA extraction with an RNA kit (RNAsimply total RNA Kit, Tiangen). Total RNA was treated with DNase I (Takara) for potential genomic DNA contamination. For qPCR analysis, 1 μg of total RNA was used to synthesize the first-strand cDNA using the PrimeScript™ RT reagent Kit (Takara) for RT-PCR in a 20-μl reaction volume according to the manufacturer’s instructions. The cDNA reaction mixture was diluted 1:10 with EASY Dilution for Real Time PCR (Takara), and 2 μl was used as the template in the 20-μl PCR reactions. PCR reactions included a pre-incubation at 95°C for 4 min, followed by 40 cycles of denaturation at 95°C for 30 s, annealing at 58°C for 30 s, and extension at 72°C for 30 s. All the reactions were performed in a 7500 Fast Real-Time PCR System (Applied Biosystems) using SYBR® Premix Ex Taq (Takara). After the PCR was run, a melting curve (65–95°C, at increments of 0.5°C) was generated to confirm the specificity of the amplification. The gene glyceraldehydes-3-phosphate dehydrogenase (BcGAPDH) was used as an internal control. The gene-specific primers that were used to detect transcripts are listed in Additional file 1: Table S1. The relative gene expression was calculated as previously described . The gene expression was measured from at least three biological replicates (three technical replicates for each biological replicate).
Pearson correlation and co-regulatory networks
To display the regulatory relationships of stress-inducible BcWRKY genes that mediated multiple abiotic stresses, the Pearson correlation coefficients of stress-inducible BcWRKY gene pairs were calculated using a house Perl script based on log2 transformed qPCR data. All of the gene pairs whose Pearson coefficient was significant at the 0.05 significance level (p-value) were collected for a gene co-regulatory network analysis. Co-expression networks were graphically visualized using Cytoscape version 2.8  based on Pearson correlation coefficients of BcWRKY gene pairs. The nodes represent genes and the edges between nodes represent gene pairs expressing correlations (hypothetical interactions). The different edge line styles indicate different correlation levels between corresponding nodes, which, in turn, indicate different interaction strengths between the co-regulated gene pairs. In addition, we compared the protein-protein relationships of stress-inducible BcWRKY orthologs in Arabidopsis using STRING 9 (http://string.embl.de/) with the default program parameter settings.
This study was supported by the National Program on Key Basic Research Projects of China (2012CB113900), the National High Tech Research Development Program of China (2012AA100100), and the National Natural Science Foundation of China (31201633) as well as the Priority Academic Program Development of Jiangsu Higher Education Institutions.
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