- Research article
- Open Access
Identification of the WRKY gene family and functional analysis of two genes in Caragana intermedia
BMC Plant Biology volume 18, Article number: 31 (2018)
WRKY transcription factors, one of the largest families of transcriptional regulators in plants, play important roles in plant development and various stress responses. The WRKYs of Caragana intermedia are still not well characterized, although many WRKYs have been identified in various plant species.
We identified 53 CiWRKY genes from C. intermedia transcriptome data, 28 of which exhibited complete open reading frames (ORFs). These CiWRKYs were divided into three groups via phylogenetic analysis according to their WRKY domains and zinc finger motifs. Conserved domain analysis showed that the CiWRKY proteins contain a highly conserved WRKYGQK motif and two variant motifs (WRKYGKK and WKKYEEK). The subcellular localization of CiWRKY26 and CiWRKY28–1 indicated that these two proteins localized exclusively to nuclei, supporting their role as transcription factors. The expression patterns of the 28 CiWRKYs with complete ORFs were examined through quantitative real-time PCR (qRT-PCR) in various tissues and under different abiotic stresses (drought, cold, salt, high-pH and abscisic acid (ABA)). The results showed that each CiWRKY responded to at least one stress treatment. Furthermore, overexpression of CiWRKY75–1 and CiWRKY40–4 in Arabidopsis thaliana suppressed the drought stress tolerance of the plants and delayed leaf senescence, respectively.
Fifty-three CiWRKY genes from the C. intermedia transcriptome were identified and divided into three groups via phylogenetic analysis. The expression patterns of the 28 CiWRKYs under different abiotic stresses suggested that each CiWRKY responded to at least one stress treatment. Overexpression of CiWRKY75–1 and CiWRKY40–4 suppressed the drought stress tolerance of Arabidopsis and delayed leaf senescence, respectively. These results provide a basis for the molecular mechanism through which CiWRKYs mediate stress tolerance.
Transcription factors are a class of proteins that significantly regulate plant growth and development and play an important role in plant defense and stress responses [1, 2]. WRKY transcription factors are one of the largest families of transcriptional regulators in plants . These transcription factors contain the WRKY domain, which is a region of 60 amino acids that is highly conserved . The WRKY domain comprises a featured WRKYGQK sequence motif and a zinc finger-like motif . The WRKY sequence is occasionally replaced by WRRY, WSKY, WKRY, WVKY or WKKY in a subset of WRKY proteins . The zinc finger structure is either CX4–5CX22–23HXH (C2H2-type) or CX7CX23HXC (C2HC-type) . At least one WRKY domain is present in all known WRKY proteins .
WRKY proteins can be classified into three main groups (group I, group II and group III) according to the number of WRKY domains along with features of the zinc finger-like motif . Group I proteins have two WRKY domains: an N-terminal WRKY domain and a C-terminal WRKY domain, with C2H2 zinc finger type CX4CX22-23HXH. Group II proteins harbor a single WRKY domain and a C2H2-type CX4–5CX23HXH zinc finger. Group III proteins contain a single WRKY domain and a C2HC-type CX7CX23HXC zinc finger . Group II WRKY proteins were further divided into five subgroups on the basis of their primary amino acid sequences: IIa, IIb, IIc, IId and IIe . Furthermore, WRKY proteins specifically bind to the W box (C/T)TGAC(T/C) DNA sequence [3, 4], and this binding requires both WRKY and zinc finger domains .
The first 4 WRKY cDNAs (SPF1, ABF (1, 2), PcWRKY (1, 2, 3) and ZAP1) were cloned from sweet potato (Ipomoea batatas), wild oat (Avena fatua), parsley (Petroselinum crispum) and Arabidopsis thaliana, respectively . Numerous WRKY proteins have been studied in various plant species. For example, there are 72 identified members in A. thaliana , 182 in soybean (Glycine max) , 127 in apple (Malus domestica Borkh.) , 80 in grape (Vitis vinifera) , 86 in Brachypodium distachyon , 85 in cassava (Manihot esculenta) , 95 in carrot (Daucus carota) , 61 in Salvia miltiorrhiza , 103 in rice (Oryza sativa) , and 32 in Broomcorn millet (Panicum miliaceum L.) . In maize (Zea mays), 136 WRKY proteins encoded by 119 WRKY genes have been identified . In cotton, 116 and 102 WRKY genes have been identified from Gossypium raimondii and Gossypium hirsutum , respectively.
WRKY transcription factors are involved in multiple plant processes, such as seed development [17, 18], dormancy  and germination , trichome development , root development , leaf senescence , plant growth and flowering [24, 25]. Notably, WRKYs have been broadly reported to be involved in plant defense responses. For instance, 49 out of 72 WRKYs from A. thaliana are differentially expressed after pathogen infection or SA treatment , and A. thaliana WRKYs including AtWRKY7, 11, 17, 18, 23, 25, 27, 38, 40, 41, 48, 53, 58, 60, and 62 serve as negative regulators of defense signaling . OsWRKY62 and OsWRKY76 of rice negatively regulate defense upon pathogen infection . Overexpression of OsWRKY13  and OsWRKY45–2  in rice increases resistance to bacterial blight and fungal blast caused by Xanthomonas oryzae pv. Oryzae and Magnaporthe grisea, respectively, while overexpression of OsWRKY42 decreases rice resistance to M. oryzae . The transcriptional regulatory cascade of WRKY13, WRKY42, and WRKY45–2 is necessary for defending rice against fungal pathogens . In cotton (G. hirsutum L.), GhWRKY15 is involved in disease resistance . Overexpression of grape VvWRKY1 in tobacco results in enhanced resistance to various fungi . The roles of WRKYs in plant responses to abiotic stresses such as drought [33,34,35,36], cold , salinity , heat [38, 39], low Pi [40, 41], ultraviolet B (UV-B) , osmotic stress , and ABA [33, 36, 44] have been widely reported. These studies suggested that WRKYs are involved in multiple stress responses.
Caragana intermedia, a native desert perennial shrub belonging to the Leguminosae family, is distributed in sandy grasslands and desert regions of west and northwest China and Mongolia, and is widely valued due to its high forage value and sand-fixing capacity, along with its strong resistance to drought and salinity [45,46,47,48]. C. intermedia is considered to be an ideal plant for elucidating the mechanisms of abiotic stress tolerance , and research on its molecular mechanisms has been increasing in recent years. For instance, to normalize quantitative real-time PCR (qRT-PCR) data from C. intermedia under different abiotic stress conditions, suitable reference genes were screened, which was useful for further gene expression analysis . The transcription of two NAC transcription factors, CiNAC3 and CiNAC4, was found to be induced under treatment with ABA and various abiotic stresses, and ectopic expression of CiNAC3 and CiNAC4 in Arabidopsis reduces the inhibition of seed germination by ABA and enhances the salt tolerance of the transgenic plants . The expression patterns of miR2118 and its target genes (CiDR1 and CiDR2) from C. intermedia are altered under drought stress, and constitutive overexpression of cin-miR2118 in tobacco enhances the plant’s tolerance to drought stress . Abiotic stresses (NaCl, ZnSO4, CdCl2, high/low temperature, and dehydration) induce the expression of the glutamate decarboxylase-encoding genes CiGAD1 and CiGAD2, except for CiGAD2 under Cd stress, and ABA has been shown to be involved in regulating the expression of CiGADs in response to salt stress . However, there is limited knowledge of the function of WRKYs in C. intermedia. In this study, we identified 53 CiWRKY genes based on transcriptomic data from C. intermedia, performed phylogenetic analysis and WRKY domain alignment, and examined the subcellular localizations of two CiWRKYs and the expression patterns of 28 of CiWRKYs in different tissues and under various abiotic stresses. Furthermore, we overexpressed CiWRKY75–1 and CiWRKY40–4 in A. thaliana and characterized their function. This work provides a basis for exploring the molecular roles of WRKYs and facilitates further investigation of the molecular mechanisms of abiotic stress tolerance in C. intermedia.
Identification and cloning WRKY genes from C. intermedia
To identify WRKYs in the drought-treated transcriptome of C. intermedia, the sequences of the A. thaliana WRKY family were used to query homologous C. intermedia sequences. After Blast searches against the sequences in NCBI using blastX to predict conserved domains and remove redundant sequences, 53 sequences with apparent WRKY domains were annotated as C. intermedia WRKY genes. Among these genes, 21 WRKYs with complete open reading frames (ORFs) were identified. Using the rapid-amplification of cDNA ends (RACE) technique, an additional 7 WRKYs were cloned, and their full-length ORFs were obtained. The ORF lengths of these 28 genes ranged from 489 bp to 2229 bp, and their amino acid lengths ranged from 163 to 743 aa (details are provided in Table 1). The 28 WRKYs with complete ORFs were used for further expression analysis.
Phylogenetic analysis and multiple sequence alignment of WRKY domains
To further analyze the evolution of these CiWRKYs, we constructed a phylogenetic tree based on a total of 140 WRKYs (72 from A. thaliana, 53 from C. intermedia and 15 from G. max distributed in different groups) (Fig. 1). According to the number of WRKY domains and the pattern of zinc finger structures, the 53 CiWRKY proteins were distributed in three main groups. Eleven CiWRKYs were assigned to group I. Thirty-four CiWRKYs were distributed in group II, which was further classified into five sub-groups: IIa, IIb, IIc, IId, and IIe, which contained 5, 6, 13, 4 and 6 CiWRKYs, respectively. The remaining 8 CiWRKYs belonged to group III.
Multiple sequence alignments of the core domains of the CiWRKYs showed that, in group I, with the exception of CiWRKY44–1, which exhibited a WKKYEEK variant sequence, all others harbored the conserved WRKYGQK sequence, and all displayed the apparent C2H2-typezinc finger (CX4CX22-23HXH). Among the 34 group II proteins containing one WRKY domain, 32 CiWRKYs carried the conserved WRKYGQK sequence, while CiWRKY50 and CiWRKY51 exhibited the WRKYGKK sequence instead. The C2H2-type zinc finger (CX4–5CX23HXH) was observed in 33 CiWRKYs. Seven of the eight group III WRKYs harbored the WRKYGQK sequence, while the variant sequence WRKYGKK was present in CiWRKY41–2. The other group III CiWRKYs exhibited C2HC-type zinc finger (CX7CX23HXC) with the exception of CiWRKY41–3 (Fig. 2).
Subcellular localization of CiWRKYs
To examine the subcellular localization of the CiWRKY proteins, one of the proteins containing two WRKY domains (CiWRKY26) and one of the proteins containing one-WRKY-domain (CiWRKY28–1) were fused with green fluorescent protein (GFP). The roots of the T2 generation of 35S::CiWRKYs-GFP transgenic Arabidopsis seedlings were used to examine GFP activity. GFP fluorescence was exclusively observed in the nuclei of the transgenic Arabidopsis seedlings, while GFP was ubiquitously present throughout the cells of the 35S::GFP transgenic lines (Fig. 3). The nuclear localization of these two CiWRKYs is in agreement with their putative roles as transcription factors.
Expression patterns of CiWRKYs in C. intermedia
The expression patterns of the 28 CiWRKYs with complete ORFs in wild C. intermedia tissues, including the roots, stems and leaves, were examined via qRT-PCR. As shown in Fig. 4 and Additional file 1: Table S1, four genes (CiWRKY3–2, CiWRKY6–2, CiWRKY23 and CiWRKY26) exhibited relatively high expression levels in all examined tissues, especially in the leaves. CiWRKY32–1, CiWRKY17 and CiWRKY15 were also ubiquitously expressed, but at relatively low levels compared with the above four genes. In contrast, the transcripts of eight genes, including CiWRKY36, CiWRKY75–1, CiWRKY12, CiWRKY50, CiWRKY28–1, CiWRKY48, CiWRKY40–4 and CiWRKY6–1, were detectable, but showed extremely low abundance in all tissues. CiWRKY28–2 and CiWRKY56 were mainly expressed in stems, while CiWRKY40–1 and CiWRKY30 were predominantly found in leaves. CiWRKY69–1 showed higher transcript abundance in the roots than in other tissues. The other CiWRKY genes showed lower expression globally, and most of them exhibited lower transcript abundance in the roots than in the leaves or stems.
Expression patterns of CiWRKYs under abiotic stresses
Malondialdehyde (MDA), proline (PRO) and soluble total sugar (SS) are indicators of plant physiological status. As shown in Additional file 2: Figure S1, drought treatment induced the accumulation of MDA, PRO and SS, whose levels peaked at 48 h. These findings indicated that the applied drought treatment was effective.
The expression patterns of the 28 of CiWRKYs were further assessed using qRT-PCR, under drought treatment as well as other abiotic stresses, including salt, abscisic acid (ABA), cold, and high-pH treatments (Table 2). The gene expression of twenty-four CiWRKYs genes was found to be induced by drought treatment, with changes of 2- to 149-fold. In contrast, the expression of CiWRKY33–1, CiWRKY15 and CiWRKY69–1 was inhibited by drought treatment, and no obvious change in the expression of CiWRKY32–1 was observed (Fig. 5). Salt treatment down-regulated the expression of 18 CiWRKYs and up-regulated the expression of 5 CiWRKYs (Additional file 3: Figure S2). Under ABA treatment, the expression of 22 CiWRKYs was increased, while that of CiWRKY3–1 and CiWRKY33–1 was decreased, and CiWRKY2, 3–2, 32–1 and 69–1 were not obviously affected (Additional file 4: Figure S3). Under cold treatment, the expression of 14 CiWRKYs was up-regulated, and the transcripts of 11 CiWRKYs were down-regulated. The expression of three other CiWRKYs presented no change compared with the expression seen in the control (Additional file 5: Figure S4). High-pH treatment enhanced the expression of 12 CiWRKYs. Notably, the maximal expression observed for CiWRKY33–1, 41–1, 50, and 40–4 corresponded to increases of 111-, 365-, 388-, and 109-fold, respectively, whereas the expression of the other CiWRKYs was not affected or even down-regulated after high-pH treatment (Additional file 6: Figure S5). The results indicated that each of these CiWRKY genes responded to at least one stress treatment.
CiWRKY75–1 transgenic Arabidopsis is hypersensitive to drought stress
CiWRKY75–1, which exhibited relatively high expression under all five treatments (Table 2), was over-expressed in Arabidopsis. Three representative overexpression lines (CiWRKY75–1-OE5, CiWRKY75–1-OE6 and CiWRKY75–1-OE8) showing relatively high expression levels were used to perform abiotic stress tolerance tests. Four-week-old transgenic Arabidopsis were exposed to drought stress by withholding watering for 15 days and were then re-watered for 3 days. The CiWRKY75–1-overexpressing lines were more sensitive to drought, displaying decreased survival rates and significantly increased MDA levels compared with the wild type (Fig. 6). No morphological differences were observed between the wild-type and CiWRKY75–1-overexpressing plants under normal growth conditions (Fig. 6). These results indicated that overexpression of CiWRKY75–1 reduced the tolerance of Arabidopsis to drought stress, and CiWRKY75–1 acted as a negative regulator in the plant response to drought.
CiWRKY40–4-overexpressing lines show delayed leaf senescence
According to the observed stress-responsive expression patterns, CiWRKY40–4 was another gene that was induced under all five treatments (Table 2). However, ectopic expression of CiWRKY40–4 in Arabidopsis resulted in no obvious morphological differences from the wild type under drought stress. Unexpectedly, under normal growth conditions, CiWRKY40–4-overexpressing Arabidopsis showed delayed leaf senescence compared with the wild type (Fig. 7). To further explore the mechanism of CiWRKY40–4 in leaf senescence, senescence related-genes, including the senescence-associated genes SAG12, SAG13 and SAG29 and the chlorophyll degradation-related genes pheophytinase (PPH), pheophorbide a oxygenase (PAO), non-yellowing1/stay-green1 (NYE1/SGR1), non-yellow coloring1 (NYC1) and NYC1-like (NOL) were analyzed. All of these genes were down-regulated in the CiWRKY40–4-overexpressing lines compared with the wild type (Fig. 8), indicating that CiWRKY40–4 delayed plant senescence by negatively regulating senescence-associated gene expression in Arabidopsis.
In this study, we identified 53 CiWRKY-encoding genes from the drought-treated transcriptome database (NCBI Sequence Read Achieve (SRA) accession number SRP121096) based on the presence of WRKY domains . According to the number of their WRKY domains and the features of their zinc finger-like motifs, the CiWRKYs were divided into three groups, as generally described, among which the group II CiWRKYs accounted for the largest proportion of 64%. These findings are consistent with reports regarding the WRKYs found in A. thaliana , cassava , and soybean , which harbor the greatest numbers of group II WRKYs in the family.
Generally, WRKY proteins are defined by the conserved amino acid sequence WRKYGQK ; however, this sequence has been replaced by WRRY, WSKY, WKRY, WVKY or WKKY in some WRKY proteins . In the present study, the WKKYEEK variant was observed in CiWRKY44–1 proteins, and the WRKYGKK variant motif replaced the conserved WRKYGQK sequence in CiWRKY41–2, 50 and 51. These findings are consistent with reports describing the WRKY proteins identified in other species, such as A. thaliana (AtWRKY51, 52 and 59) , V. vinifera L. (VvWRKY8, 13, 14 and 24) , and P. miliaceum L. (PmWRKY2, 15, 23, 24, and 28) .
According to recent reports , several of the WRKYs have more than 2 WRKY domains or contain other domains, in addition to the WRKY domains. These other domains include, for example, the ZF_SBP TF domain, kinase domain, PAH domain, ULP_protease domain, TIR domain, LRR domains, NAC domain, ATP_GRASP domain, and B3 domain. Based on these findings, additional novel groups, beyond the three known WRKY groups, were identified . In A. thaliana, Fragaria vesca, Brassica rapa, G. max, G. raimondii, and Sorghum bicolor, 1, 5, 3, 1, 2, and 3 novel WRKY proteins have been found, respectively . We report here that all of the 28 identified CiWRKYs with ORFs contained one or two WRKY domains. In addition to the WRKY domains, NCBI conserved domain database (CDD) annotation  showed that CiWRKY36 (Group IIb) contains a DUF972 (domain of unidentified function 972) domain, followed by a WRKY domain, and both CiWRKY15 and CiWRKY17 (Group IId) harbor a plant_Zn_cluster domain, which is located at the N-terminus and is followed by a WRKY domain. CiWRKY6–1 (Group IIb) exhibits a bZIP (basic region/leucine zipper) domain, followed by a WRKY domain. DUF972 belongs to a protein family of unknown function. The plant_Zn_cluster domain is present in two CiWRKYs (CiWRKY15 and CiWRKY17) and is located at the N-terminus of the WRKY domain. Its sequence (EHSDDVSGSGKCHCVKRRKNRVKRTVRVPAISSKIAD) is different from the zinc finger structure, and this domain may have additional functions. bZIP transcription factors are also one of the largest gene families in plants and are involved in multiple plant biological processes, including various stress responses [56, 57].
Evidence from genome- or transcriptome-wide analyses shows that the response of WRKYs to abiotic stresses varies according to the species. For instance, 30 putative WRKYs were identified through transcriptome analysis in Chinese wild hazel (Corylus heterophylla Fisch), and 23 of these WRKYs were found to be simultaneously up-regulated by cold, drought and high-salinity stresses . Twenty-eight salt-responsive GarWRKYs were identified among 109 WRKY genes in a salt-tolerant wild cotton species (Gossypium aridum) based on transcriptome sequencing data . In P. miliaceum L., 32 WRKYs were identified based on transcriptome analysis, and the expression levels of 22 PmWRKYs were observed to be significantly altered under at least one abiotic stress treatment . Among the 85 WRKY genes identified from the M. esculenta genome, 78 were found to be differentially expressed in response to drought stress . In addition, 34 out of 127 WRKYs from the apple genome were identified as differentially expressed under water-logging stress .
Drought is one of the most common environmental stress factors that significantly inhibits plant growth and crop production . The roles of the WRKY transcription factors in the drought response have been widely reported. Activated or constitutive expression of WRKY57 confers drought tolerance in A. thaliana , and the expression of AtWRKY57 is increased by abiotic stresses such as ABA, dehydration, and mannitol treatment . Overexpression of AtWRKY53 results in hypersensitivity to drought stress by inhibiting stomatal closure . Overexpression of TaWRKY1 and TaWRKY33 in Arabidopsis leads to enhanced plant drought tolerance . WRKY20 transcripts accumulate in wild soybean (G. soja) under ABA, salt, cold, and drought stresses, and overexpression of GsWRKY20 increases the drought tolerance in A. thaliana .
We performed a transcriptome analysis to profile gene expression patterns in C. intermedia in response to drought stress and identified 53 CiWRKY genes with varying expression patterns in response to drought stress (Additional file 7: Table S2). Further investigation showed that the transcripts of 28 CiWRKYs (with complete ORFs) responded to at least one abiotic stress when plants were subjected to drought, cold, salt, high-pH, and ABA treatments. The expression levels of fifteen genes (CiWRKY12, 17, 15, 28–1, 30, 33–1, 40–1, 50, 51, 48, 56, 26, 75–1, 40–4, and 6–2) were altered under all five treatments. Notably, CiWRKY40–1 and CiWRKY75–1 responded to all treatments intensively. In A. thaliana, AtWRKY75, which is a homologue of CiWRKY75–1 sharing 85% amino acid sequence similarity, has been reported to regulate Pi starvation and root development  and to play a role in plant resistance to pathogens [64, 65]. In the present study, the overexpression of CiWRKY75–1 in Arabidopsis compromised the drought stress tolerance of plants. This finding has not been reported by other researchers, and suggests that CiWRKY75–1 serves as a negative regulator under drought stress. Both the mRNA and protein of AtWRKY53 are reported to accumulate in Arabidopsis following drought stress, and AtWRKY53 overexpression enhances hypersensitivity to drought stress compared with that in the wild type, via inhibition of stomatal closure to increase the water loss rate . The AtWRKY46 transcript is also induced by drought stress in Arabidopsis , and the AtWRKY46/54/70 signaling complex negatively regulates plant drought tolerance by repressing dehydration-inducible gene expression, which is likely achieved via the simultaneous function of BES1 . However, all four Arabidopsis WRKYs belong to group III, while CiWRKY75–1 belongs to group IIc; thus, the mechanism underlying the regulation of the drought tolerance signaling pathway by CiWRKY75–1, either through direct or indirect interaction with downstream genes, remains unclear. Additionally, no morphological differences during root development were observed between the overexpression lines and wild-type Arabidopsis, and the functions of CiWRKY75–1 in pathogen infection and Pi starvation still require further investigation.
CiWRKY40–4 is in the same group IIa clade as WRKY40, WRKY18, and WRKY60 of A. thaliana and is most similar to AtWRKY40. In A. thaliana, WRKY18, WRKY40 and WRKY60 play partially redundant roles in response to P. syringae and B. cinerea infection . The wrky18wrky40 double mutant displays enhanced resistance towards the powdery mildew Golovinomyces orontii. This mutant is also involved in PAMP-triggered basal defense and acts as a negative regulator of positive defense regulators such as CYP71A13, EDS1 and PAD4 . In addition, the expression of WRKY40, WRKY18, and WRKY60 is elevated under ABA, NaCl and PEG treatments . The wrky40 knockout mutant of A. thaliana exhibits a sensitive phenotype, while WRKY40-overexpressing lines show a less sensitive phenotype than the wild type under ABA-induced inhibition of seed germination . WRKY40 represses the ABA-responsive genes, such as ABI5, and functions as negative regulator of in ABA signaling by interacting with ABAR . AtWRKY40 acts as a negative regulator of pathogen-induced cell death regulated by NAC4 . The transcription of WRKY40, WRKY46, WRKY51, WRKY60, WRKY63, and WRKY75 is elevated in a loss-of-function mutant of FtSH4, which encodes a mitochondrial protease that is involved in SA-mediated leaf senescence . In the present study, overexpressing CiWRKY40–4 in A. thaliana did not alter drought tolerance but delayed leaf senescence by down-regulating the expression levels of senescence-related genes. Senescence is the final step in leaf development and allows nutrients from old leaves to be salvaged . SAGs, which are markers of senescence, are up-regulated in the senescing leaves of A. thaliana . Overexpression of SAG29 has been shown to result in accelerated senescence, and osmotic stresses, such as high salinity, cold, and drought, induce the accumulation of its transcripts .
NYC1 and NOL encode chlorophyll b reductase, which is involved in the biochemical pathway of chlorophyll degradation  and accelerates the reduction reaction of chlorophyll b in conversion to chlorophyll a [73, 76]. PPH is an essential enzyme for chlorophyll breakdown that catalyzes the transformation of pheophytin a (Mg-free chlorophyll a) into pheophorbide a , which is then converted to a red chlorophyll catabolite by PAO . The activity of PAO is modulated by NYE1, which is also known as SGR1 [79, 80]. In A. thaliana, a PPH-deficient mutant (pph-1) exhibits a stay-green phenotype due to the prevention of chlorophyll degradation during senescence . The Atnye1, Atpao1, Osnol1 and Osnyc1 mutants all exhibit a stay-green phenotype under natural and/or induction conditions [73, 76, 79, 81]. The down-regulation of SAGs (12, 13 and 29), NYC1, NOL, PPH, PAO and NYE1/SGR1, in CiWRKY40–4-overexpressing Arabidopsis indicates that CiWRKY40–4 delays Arabidopsis leaf senescence by directly or indirectly down-regulating these genes; however, further investigation will be required to elucidate the mechanism.
Taken together, these results indicate that different CiWRKYs play different roles in plant responses to abiotic stress and developmental processes. Hence, there is an urgent need for examination of the function of CiWRKYs in tolerance against abiotic stresses in C. intermedia in future studies.
In this study, 53 WRKY sequences were retrieved from the drought-treated transcriptome of C. intermedia, among which 28 CiWRKYs exhibited full-length sequences. This is the first study to analyze WRKY family genes in C. intermedia based on transcriptome data. The predicted proteins were grouped via phylogenetic tree analysis with WRKYs from A. thaliana and G. max, and their WRKY domains were characterized through multiple sequence alignment of the CiWRKY genes. Furthermore, the subcellular localization of both CiWRKY28–1, with one WRKY domain, and CiWRKY26, with two WRKY domains, is nuclear. The majority of the 28 CiWRKYs with full-length sequences are expressed in more than one tissue. The expression patterns of the 28 CiWRKYs in response to different abiotic stresses (drought, salt, cold, high-pH and ABA) were examined, and the abiotic stress-responsive genes were further evaluated. Additionally, overexpression of CiWRKY75–1 and CiWRKY40–4 in A. thaliana resulted in hypersensitivity to drought stress and delayed leaf senescence, respectively, compared with the wild type. The results of this study will be useful for understanding the involvement of WRKY genes in stress resistance and plant development and will provide the basis for future functional studies on WRKYs.
WRKY identification, phylogenetic analysis and multiple sequence alignment
CiWRKY sequences were derived from a drought-treated RNA-seq database of C. intermedia, in which dehydration treatment was performed by placing the whole seedlings on filter paper for 1, 3 or 12 h. The dataset was submitted to NCBI SRA under the accession number SRP121096. The WRKY sequences of A. thaliana and G. max were downloaded from the TAIR database (The Arabidopsis Information Resource: http://www.arabidopsis.org/) and the JGI database (https://phytozome.jgi.doe.gov), respectively.
The conserved protein domains were subjected to Blast searches against the NCBI database (https://blast.ncbi.nlm.nih.gov/Blast.cgi?PROGRAM=blastx&PAGE_TYPE=BlastSearch&LINK_LOC=blasthome) using blastx. After the removal of redundant sequences and WRKY domain prediction, a total of 53 putative CiWRKYs containing the WRKY domain were obtained, which were named according to their similarity with Arabidopsis WRKYs.
A phylogenetic tree of CiWRKYs was constructed using MEGA6.0 and the neighbor-joining (NJ) method, with 1000 bootstrap replications, based on the amino acid sequences of A. thaliana and G. max WRKY proteins.
DNAMAN7 software was used to analyze the core sequences of the WRKY domain via multiple sequence alignment.
Plant materials and abiotic stress treatments
Seeds from wild C. intermedia were collected from Wulanchabu City, Inner Mongolia Autonomous Region, China (41.44N, 111.69E). No specific field permissions were required to collect the plant samples. The plant material used in this study had been formally identified by Dr. Liwang Qi (Chinese Academy of Forestry), Prof. Ling Yan (Inner Mongolia Agricultural University) and Prof. Meng Ji (Inner Mongolia Academy of Forestry).
The seeds were sown in pots containing peat soil and vermiculite (1:2 v/v) under long-day conditions (16-h-light/8-h-dark cycle) at 22 °C. One-month-old plants were employed for the abiotic stress treatments, as previously described [51, 82]. Briefly, prior to the drought, salt, high-pH (10) and ABA treatments, whole seedlings were removed from soil and cleaned with tap water. For drought treatment, whole seedlings were placed on filter paper for 0.5, 1, 3, 6, 12, 24 or 48 h at room temperature. For the salt, high-pH (10) and ABA treatments, the roots of the seedlings were soaked with solutions containing 300 mM NaCl, 200 mM NaHCO3 (using NaOH to adjust the pH to 10) or 100 μM ABA, respectively, for 0.5, 1, 3, 6, 12, 24 or 48 h. For cold treatment, pots containing seedlings were transferred to 4 °C and then cultured for 0.5, 1, 3, 6, 12, 24 or 48 h. Untreated plants were used as controls. At each time point in each treatment, the shoots of three plants were harvested as one sample; each plant was only used once for tissue harvesting, at one time point, and was not subjected to any further treatment thereafter. Samples were snap frozen in liquid nitrogen and stored at − 80 °C until they were employed for total RNA extraction. All experiments were repeated three times.
Additionally, the roots, stems, and leaves of wild C. intermedia were collected during the flowering stage for tissue-specific expression analysis.
The leaves of four-week-old wild-type and transgenic Arabidopsis were used for relative gene expression analysis.
PRO, SS and MDA measurements
One-month-old C. intermedia seedlings cultured in growth chambers were subjected to drought treatment, and physiological indices were measured at different time points (0, 1, 3, 6, 12, 24 or 48 h). The contents of PRO, MDA and SS were determined in colorimetric assays, using the ninhydrin coloration, thiobarbituric acid and anthrone methods, respectively .
Total RNA extraction and cDNA synthesis
Total RNA was isolated from samples using the TRIzol regent. For tissue-specific expression, RNA was extracted from different tissues, including the roots, stems, and leaves. For the examination of abiotic stress-responsive expression, RNA was extracted from shoots. For gene expression analysis in Arabidopsis, RNA was extracted from leaves. RNA integrity was examined through agarose gel electrophoresis, and RNA purity was determined based on the A260 nm/A280 nm and A260 nm/A230 nm ratios.
After pretreatment with RNase-free DNase I (Takara, Dalian, China), total RNA (1 μg), was used to synthesize first-strand cDNA employing an M-MLV reverse transcriptase kit (Takara) according to the manufacturer’s instructions. The cDNA was then diluted 16-fold to be employed as a template for qRT-PCR analysis.
qRT-PCR analysis of gene expression
qRT-PCR was performed using SYBR Premix Ex Taq II (Takara) on a LightCycler 480 Real Time PCR system (Roche, Basel, Switzerland), as previously described . The thermal cycling program was as follows: 95 °C for 30 s, followed by 40 cycles of 95 °C for 5 s, 60 °C for 30 s and 72 °C for 15 s. CiEF1α (GenBank: KC679842)  was employed as a reference gene to normalize target gene expression levels in the C. intermedia samples, and the 2-ΔΔCT and 2-ΔCT methods  were used to calculate the relative expression levels of stress-responsive and tissue-specific genes, respectively. AtEF1α (At5G60390)  was employed as a reference gene for the normalization of target gene expression levels in Arabidopsis samples via the 2-ΔΔCT method . Three technical replicates for each reaction were performed. The primers employed for qRT-PCR analysis are listed in Additional file 8: Table S3.
CiWRKY transgenic A. thaliana
To generate the recombinant CiWRKY overexpression vector, the full-length CDSs of CiWRKY75–1 and CiWRKY40–4 were amplified using PCR product from wild C. intermedia cDNA and cloned into the expression vector pCanG-HA using the restriction enzymes SalI/SpeI and SacI/SalI, respectively.
To generate the recombinant CiWRKY and GFP-infused vectors, the coding sequences of CiWRKY26 and CiWRKY28–1 without the stop codon were amplified using PCR, and the PCR products were then cloned into the N- terminus of the GFP-encoding sequence in the pCAMBIA1302 vector driven by the cauliflower mosaic virus (CaMV) 35S promoter. The primers used for the construction of all of the recombination vectors are listed in Additional file 8: Table S3.
The recombinant vectors were expressed in wild-type A. thaliana using the floral dipping method , mediated by Agrobacterium tumefaciens (strain GV3101). The empty vector was used as the control.
Subcellular localization of CiWRKYs
The roots of 10-day-old T2-generation transgenic seedlings were employed for observations of GFP fluorescence under an LSM510 confocal laser-scanning microscope (Carl Zeiss), with 488 nm argon excitation and a 505–530 nm band filter, as previously described .
Drought tolerance test
To assess the potential drought tolerance of the CiWRKY-overexpressing lines, four-week-old transgenic plants and wild-type plants growing in the same pots were exposed to drought stress by withholding water for 15 days, and the plants were then re-watered and allowed to grow for an additional 3 days. Survival rates were calculated using 30 plants per genotype for each experiment. The leaf samples were harvested before or immediately after drought treatment to measure physiological indices. This experiment was repeated three times with similar results.
Green fluorescent protein
- NOL :
- NYC1 :
- NYE1/SGR1 :
Open reading frame
- PAO :
Pheophorbide a oxygenase
- PPH :
Quantitative real-time PCR
Rapid-amplification of cDNA ends
Soluble total sugar
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We thank Dr. Yan Wang for critical reading the manuscript, and thank Nature Research Editing Service for language editing.
This work was supported by National Natural Science Foundation of China (No.31360169), and Inner Mongolia Science & Technology Plan (201503004). The funding bodies only provide the financial support in the design of the study and collection, analysis, and interpretation of data and in editing the manuscript.
Availability of data and materials
The transcriptome clean raw reads data that support the findings of this study have been deposited in NCBI Sequence Read Archive (https://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/Traces/sra_sub/) under the accession number SRP121096. The sequence of CiWRKYs analyzed during the current study is available from the corresponding author on reasonable request. Other relevant data analyzed during this study are included in this published article and its supplementary information files.
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Expression data for CiWRKY genes in different C. intermedia tissues. The expression data were generated via qRT-PCR, and calculations were performed using the 2-ΔCT method; CiEF1α was used as an endogenous control. (XLS 22 kb)
Changes in physiological activity in C. intermedia under drought treatment. The abscissa indicates the time points in the treatments, and the ordinate indicates physiological activities. (a) MDA content. (b) Pro content. (c) SS content. (PDF 112 kb)
Expression patterns of CiWRKYs under salt treatment. Samples were collected from the shoots of one-month-old C. intermedia seedlings at 0.5, 1, 3, 6, 12, 24 or 48 h following salt treatment, and untreated plants were employed as the control. The expression levels of 28 CiWRKYs with full-length sequences were examined via qRT-PCR. Expression values were estimated using the 2-ΔΔCT method, and CiEF1α was used as reference gene. The error bars represent the means of three technical replicates ± SD. (PDF 258 kb)
Expression patterns of CiWRKYs under ABA treatment. Samples were collected from the shoots of one-month-old C. intermedia seedlings at 0.5, 1, 3, 6, 12, 24 or 48 h following ABA treatment, and untreated plants were employed as the control. The expression levels of 28 CiWRKYs with full-length sequences were examined via qRT-PCR. Expression values were estimated using the 2-ΔΔCT method, and CiEF1α was used as reference gene. The error bars represent the means of three technical replicates ± SD. (PDF 254 kb)
Expression patterns of CiWRKYs under cold treatment. Samples were collected from the shoots of one-month-old C. intermedia seedlings at 0.5, 1, 3, 6, 12, 24 or 48 h following cold treatment, and untreated plants were employed as the control. The expression levels of 28 CiWRKYs with full-length sequences were examined via qRT-PCR. Expression values were estimated using the 2-ΔΔCT method, and CiEF1α was used as reference gene. The error bars represent the means of three technical replicates ± SD. (PDF 253 kb)
Expression patterns of CiWRKYs under high-pH treatment. Samples were collected from the shoots of one-month-old C. intermedia seedlings at 0.5, 1, 3, 6, 12, 24 or 48 h following high-pH treatment, and untreated plants were employed as the control. The expression levels of 28 CiWRKYs with full-length sequences were examined via qRT-PCR. Expression values were estimated using the 2-ΔΔCT method, and CiEF1α was used as reference gene. The error bars represent the means of three technical replicates ± SD. (PDF 257 kb)
Expression data for 28 CiWRKY genes with complete ORFs based on drought-treated transcriptome data. (XLS 22 kb)
Primers employed for qRT-PCR and the analysis of transgenic plant construction. (XLS 27 kb)
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Wan, Y., Mao, M., Wan, D. et al. Identification of the WRKY gene family and functional analysis of two genes in Caragana intermedia. BMC Plant Biol 18, 31 (2018). https://0-doi-org.brum.beds.ac.uk/10.1186/s12870-018-1235-3
- WRKY gene family
- Caragana Intermedia
- Abiotic stress
- Gene expression
- Subcellular localization
- Function analysis