The walnut transcription factor JrGRAS2 contributes to high temperature stress tolerance involving in Dof transcriptional regulation and HSP protein expression
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GRAS transcription factor (TF) family is unique and numerous in higher plants with diverse functions that involving in plant growth and development processes, such as gibberellin (GA) signal transduction, root development, root nodule formation, and mycorrhiza formation. Walnut tree is exposed to various environmental stimulus that causing concern about its resistance mechanism. In order to understand the molecular mechanism of walnut to adversity response, a GRAS TF (JrGRAS2) was cloned and characterized from Juglans regia in this study.
A 1500 bp promoter fragment of JrGRAS2 was identified from the genome of J. regia, in which the cis-elements were screened. This JrGRAS2 promoter displayed expression activity that was enhanced significantly by high temperature (HT) stress. Yeast one-hybrid assay, transient expression and chromatin immunoprecipitation (Chip)-PCR analysis revealed that JrDof3 could specifically bind to the DOFCOREZM motif and share similar expression patterns with JrGRAS2 under HT stress. The transcription of JrGRAS2 was induced by HT stress and up-regulated to 6.73-~11.96-fold in the leaf and 2.53-~4.50-fold in the root to control, respectively. JrGRAS2 was overexpressed in Arabidopsis, three lines with much high expression level of JrGRAS2 (S3, S7, and S8) were selected for HT stress tolerance analysis. Compared to the wild type (WT) Arabidopsis, S3, S7, and S8 exhibited enhanced seed germination rate, fresh weight accumulation, and activities of catalase (CAT), peroxidase (POD), superoxide dismutase (SOD) and glutathione-S-transferase (GST) under HT stress. In contrast, the Evans blue staining, electrolyte leakage (EL) rates, hydrogen dioxide (H2O2) and malondialdehyde (MDA) content of transgenic seedlings were all lower than those of WT exposed to HT stress. Furthermore, the expression of heat shock proteins (HSPs) in S3, S7, and S8 was significant higher than those in WT plants. The similar results were obtained in JrGRAS2 transient overexpression walnut lines under normal and HT stress conditions.
Our results suggested that JrDof3 TF contributes to improve the HT stress response of JrGRAS2, which could effectively control the expression of HSPs to enhance HT stress tolerance. JrGRAS2 is an useful candidate gene for heat response in plant molecular breeding.
KeywordsTranscriptional regulation Promoter Dof transcription factor GRAS transcription factor High temperature stress
Cetyltrimethylammonium ammonium bromide
Heat shock protein
Murashige and skoog
Quantitative real-time PCR
Reactive oxygen species
Synthetic drop-out medium
3-amino-1, 2, 4-triazole
High temperature (HT) stress is one of the most important limiting factors to plant growth and productivity ; warming surface temperatures and increasing frequency and duration of widespread droughts threaten the health of natural forests and agricultural crops . The rising temperature may cause a change in the growing periods and the distribution of plants. HT may inactivate major enzymes, disturb protein synthesis, damage proteins and membranes, have major effects on the process of cell divisions, all of these can favor the oxidative damage and seriously limit the plant growth [1, 3]. Other than this, long-term HT stress during the seed filling can result in poor quality and low yield [4, 5, 6]. For instance, the number of spikes and florets per plant in rice and the seed-set in sorghum were negatively affected by HT stress [7, 8]. Under high night temperature, a decrease in individual grain weight resulted in significant reduction in rice grain production per unit area . Zhao et al. (2017) point out that without effective adaptation, CO2 fertilization, and genetic improvement, each degree-Celsius increase in global mean temperature would, on average, reduce global yields of maize by 7.4%, wheat by 6.0%, rice by 3.2%, and soybean by 3.1% . Therefore, the damage caused by HT to plants should not be underestimated.
The effect of HT varies in different plant species and cultivars, and even at different developmental stages within a species. To enable the production of plants with improved thermotolerance, decoding the mechanisms that which plants cope with HT is very necessary . In recent years, physiological, biochemical, genetic, and molecular studies have revealed a number of vital cellular components and processes involved in thermoresponsive growth and the acquisition of thermotolerance in plants . During these processes, a series of genes are employed that including heat shock proteins (HSPs) and reactive oxygen species (ROS)-scavenging enzymes, which were classified into two groups as follows: (1) The genes involve in heat shock signaling mechanisms that mainly including HSFA1-dependent transcriptional regulation networks, HSFA1-independent transcription regulation networks, Calcium (Ca2+) signaling, ROS signaling, NO signaling, Hydrogen sulfide (H2S) signaling, and unfolded protein response (UPR) [11, 12, 13, 14, 15, 16, 17, 18, 19, 20]. (2) The genes associate with high ambient temperature signaling mechanisms, which contain the coordinated regulation of circadian clock , phytohormone signaling , and light signaling . The core of these various signaling pathways is partially integrated to the basic helix-loop-helix (bHLH) transcription factor (TF) phytochrome interacting factor 4 (PIF4) [11, 21, 22]. PIF4 is connected with abundant genes such as: ultraviolet (UV) resistance locus 8 (UVR8) , constitutively photomorphogenic 1 (COP1) , elongated hypocotyl 5 (HY5) . In PIF4-dependent ambient HT responses, PIF4 can activate the expression of auxin biosynthesis-related genes such as cytochrome P450, YUCCA 8 (YUC8), and tryptophan aminotransferase of Arabidopsis 1 (TAA1) via binding to their promoters [27, 28]; PIF4 can synergistically promote the transcription of genes required for hypocotyl elongation such as auxin response factor 6 (ARF6) ; In addition, PIF4 can integrate brassinosteroid (BR) and gibberellin (GA) signaling by interacting directly with their central components [29, 30].
In GA signaling, the GRAS TF family is one of the important members, which is unique to higher plants and discovered in recent years. The name of GRAS is derived from the three initially identified members, GA insensitive (GAI), repressor of GA1 (RGA) and scarecrow (SCR) . In addition to play the role in GA signal transduction, studies have demonstrated that GRAS TFs play diverse roles in light signaling, root and meristem development, biotic and abiotic stress responses . According to functional differences and structural characteristics, GRAS TFs were divided into several sub-families such as DELLA, SCR, SHR, SCL3, PAT, and LISCL . Among which, the SCL proteins were considered as members of HT stress response signal pathway. For instance, the levels of cabbage GRAS TF BoSCL13 was increased with heat shock and confirmed as a unique candidate gene for discriminating heat shock tolerance in cabbage breeding . The transcription of AtSCL13 (At4g17230) was increased by heat shock at an early time point after heat treatment . However, the reports on GRAS to HT stress are few, future studies on the specific roles of GRAS TFs in heat tolerance and/or heat response is necessary.
Juglans regia is a nut tree cultivated worldwide and famous for its nutritious fruits . As in all other plant species, walnut tree is sessile and cannot escape the unfavorable environmental conditions . The growth, development, and production of J. regia are all affected by environmental stimulus, such as: high temperature, cold, salinity, and drought stress [37, 38]. However, studies on the stress response mechanism of walnut trees are currently lacking; achieving a better understanding of the mechanisms involved in abiotic stress response of J. regia is timely and essential . In previous studies, we identified a few candidate genes from walnut tree relating to stress response, including some members of GRAS TF family, among which a SCL protein (Named as JrGRAS2) was detected to be induced by HT, and could improve the heat tolerance of yeast . In this study, we further explore the function mechanism of JrGRAS2 response to HT stress, and found JrGRAS2 is a positive factor for plant HT tolerance associating with Dof TF and HSP protein.
Identification and HT stress response of JrGRAS2 promoter
JrDof3 acts as the up-stream regulator of JrGRAS2 in HT stress response
Overexpression of JrGRAS2 up-regulated plant HT stress tolerance
JrGRAS2 improves plant HT tolerance involving in HSP expression
Walnut is an important economic tree and affected by HT stress as other plant species, whose adaptation and response mechanisms on HT are currently insufficiently studied. Considering the abundant members of GRAS in walnut genome, the potential role of SCL subfamily GRAS TFs in HT stress response , and the HT stress response function and molecular mechanism of GRAS remains to be elucidated, in this study, a SCL GRAS was cloned from J. regia (named as JrGRAS2) and the up-stream regulation mechanism involving in HT stress response was characterized. The isolated up-stream promoter was heterologous transformed into Arabidopsis and homologous transient expressed in walnut, which displayed various GUS activities in different tissue parts and were enhanced by HT treatment (Fig. 1). Since the expression activity of the promoter is usually related to its function, for instance, the expression of Tamarix hispida V-ATPase c subunit (ThVHAc1) promoter was up-regulated by CdCl2 and ThVHAc1 was further confirmed as Cd tolerance gene ; the promoter expression activity of Cd-resistance gene JrVHAG1 (walnut V-ATPase G subunit) was induced by CdCl2 ; transformation of the banana aquaporin family gene MaTIP1;2 promoter into Arabidopsis to assess its function indicated that it responds to both drought and salt stress treatments ; it can be learn that JrGRAS2 is a potential HT stress tolerance gene.
The JrGRAS2 promoter is consist of diverse cis-elements those were classified into different subfamilies. In detail, twenty-six, nineteen, thirteen, eight, seven and five different elements were belong to the classes of ‘ABA, Dehydration and salinity (osmotic) stress responsive’, ‘Tissue/organelles specific expression’, ‘Light responsive’, ‘Phytohormone responsive’, ‘Pathogen, elicitor and wound responsive’ and ‘Heat and cold stress related’, respectively (Additional file 2: Table S1), according to the reports from Vivekanand Tiwari et al , suggesting the potential abundant regulation function of this promoter. Among all the elements, DOFCOREZM motif is the most one (Additional file 2: Table S1). Meanwhile, Dof TFs were reported as the effective factors in plant stress response, such as salt, drought, cold and heat [46, 47], therefore, DOFCOREZM motif was picked up for yeast one-hybrid assay to screen for the potential up-stream regulators of JrGRAS2, and the results showed that JrDof3 could specially bind to the DOFCOREZM motif (Fig. 2) that functioned as an up-stream regulator of JrGRAS2, which were further confirmed by co-transient expression and Chip-PCR analysis (Figs. 3, 4).
The target gene responds to stress are usually regulated by the upstream regulators binding or unbinding to the motifs in the promoter [43, 45]. Since the promoter expression activity of JrGRAS2 was enhanced by HT (Fig. 1) and JrGRAS2 is speculated as a potential HT tolerance gene, the transcription of JrDof3 and JrGRAS2 exposed to HT treatment was analyzed by qRT-PCR and both showed positive response to HT stress (Fig. 5). For induced transcription is a prediction for potential function in plant stress response, such as: Tamarix ThVHAc1 was up-regulated by CdCl2 then confirmed as a Cd tolerance gene ; walnut JrGSTTau1 was induced by cold and further characterized as a chilling tolerance factor ; tomato SlGRAS40 was upregulated by D-mannitol or NaCl, which was verified as drought and salt resistance TF , we can conclude that the HT stress response of JrGRAS2 is controlled by JrDof3 which may act as an up-stream regulator of JrGRAS2 to either control or act together with JrGRAS2 to participate in plant HT stress response.
To complete confirm the HT stress response function of JrGRAS2, it was overexpressed in Arabidopsis and three transgenic lines S3, S7 and S8 were selected for analysis. Interestingly, the expression of JrGRAS2 is effective to improve plant HT stress tolerance which was demonstrated by germination ability, growth efficiency, ROS accumulation and antioxidant activity (Fig. 6, 7 and 8). And the parallel results were obtained in transient overexpression walnut lines exposed to HT treatment (Fig. 9). The similar results here were observed in the plants overexpression of JrGSTTau1 that the transgenic plants accumulated less ROS, more biomass and higher activities of SOD, POD than WT plant under cold stress ; overexpression of the wheat F-Box protein gene TaFBA1 enhanced heat stress tolerance in transgenic tobacco owing to the growth inhibition was reduced and photosynthesis was increased as compared with those in WT plants ; Malus sieversii MsHsp16.9 is proved to be a protein chaperone that attenuate plant responses to severe stress via positively regulates antioxidant enzyme activity . Therefore, we believe that JrGRAS2 is a vital HT stress responsive gene for walnut tree in temperature adaption regulation.
Plant TFs usually participate in stress response by regulating downstream related genes , for instance, unconventional splicing of wheat TabZIP60 could contribute to heat tolerance in transgenic plants by modulating the expression of ER stress-related genes ; Vitis amurensis GRAS TF VaPAT1 confers abiotic stress tolerance via up-regulate stress-related genes such as AtSIZ1, AtCBF1, AtATR1/MYB34, AtMYC2, AtCOR15A, AtRD29A and AtRD29B ; Tamarix eukaryotic translation initiation factor 1A (eIF1A) connected to the expression of stress-related genes, TOBLTP, GST, MnSOD, NtMPK9, poxN1 and CDPK15, in salt and drought stress response . Since the HSP proteins were important HT stress-related members [6, 52, 55], the Arabidopsis HSP genes were identified from the TAIR database and analyzed in JrGRAS2 overexpression Arabidopsis plants, whose transcription were enhanced in S3, S7 and S8 compared to those in WT plants (Fig. 10); meanwhile, the HSPs from walnut tree were also up-regulated by JrGRAS2 in transient expression lines TS1 and TS2 (Fig. 9a); these findings were similar to the up-regulation of HSP genes in heat-tolerant csd1, csd2 and ccs plants while reduced in heat-sensitive transgenic plants expressing miR398-resistant forms of CSD1, CSD2 or CCS ; overexpression of HsfA1a had positive effects on the tolerance to diverse stressors by promoting inducible of Hsp expression . Therefore, based on these findings, we defined that JrGRAS2 endows plant HT stress tolerance was partially by regulating the expression of HSP genes.
The JrGRAS2 promoter includes abundant stress related cis-elements and could be induced by HT stress, implying the positive role of JrGRAS2 in HT stress response. Yeast one-hybrid, transient expression, Chip-PCR and qRT-PCR assays confirmed that JrDof3 was a potential up-stream regulator of JrGRAS2 for HT stress resistance. Heterologous and homologous overexpression of JrGRAS2 in Arabidopsis and walnut revealed that JrGRAS2 is an effective TF for plant HT stress tolerance, which was involved in growth, ROS scavenging and antioxidant metabolism. These results indicated that JrGRAS2 is an important candidate gene for plant HT stress tolerance in molecular breeding, and it will offer new insights to reveal the adverse stimulus adaptation mechanism of walnut trees.
Plant materials and treatments
Two-year-old grafted ‘Xiangling’ (a genotype of J. regia widely planted in China, in this study, the seedlings were obtained from Walnut Experimental Station, Northwest A & F University) seedlings were grown in a greenhouse with the relative humidity 70±5%, temperature 22±2°C, illumination cycle 14/10 h) , and treated with 37°C for 0 (control), 1, 3, 6, and 12 h. The leaves and roots were harvested independently and frozen in liquid nitrogen, then stored at -80°C for total DNA and RNA isolation, which were used as the template of promoter cloning and qRT-PCR analysis, accordingly. The treatment at each time point was applied three times and each treatment contained 9 seedlings.
Identification and expression activity of the JrGRAS2 promoter
The J. regia leaves was used to extract the genomic DNA by CTAB (cetyltrimethylammonium bromide) method with after ground in liquid nitrogen and cleaned in a 0.14 M NaCl solution. The DNA quality was confirmed by electrophoresing in 1.0 % agarose gel and staining with ethidium bromide (EB). The JrGRAS2 promoter was identified from the walnut genome , and amplified by PCR reaction from the J. regia DNA. The PCR amplification parameters were set as follows: 30 s at 94°C followed by 35 cycles at 94°C for 30 s, 58°C for 30 s, 72°C for 90 s, and at 72°C for 7 min extending. The 20 μL PCR reaction mixture was generated according to manufacturer instructions (Takara Ex Taq®, Takara, Dalian, China). The cis-elements in the JrGRAS2 promoter were categorized into different groups after the analysis using the online programs PLACE  and PLANTCARE . The expression activity of JrGRAS2 promoter (JrGRAS2-P) was functionally validated by a transgenic approach: The 35S promoter was replaced by the JrGRAS2 promoter to drive the expression of β-glucuronidase (GUS) gene in a pCAMBIA1301 vector to generate a recombinant construct pCAM-JrGRAS2-P, which was used for Arabidopsis plant transformation using Agrobacterium-mediated floral dip method . Five-week-old transgenic seedlings were used to study the expression activity and level through GUS activity determination and staining [42, 61] under normal and HT stress (37°C). Meanwhile, the pCAM-JrGRAS2-P was transient transformed into walnut leaves using Agrobacterium-mediated method. The EHA105(pCAM-JrGRAS2-P) cells were grown to OD600=0.8~1.0, then diluted to OD600=0.05~0.1 with 1/2MS (Murashige and Skoog) liquid medium plus with 100 μM acetosyringone (AS). The three-month-old J. regia leaves were immersed in this solution and incubated for 8~10 h at 25°C with 40~50 rpm shaking, rinsed third with 1/2MS and incubated in fresh 1/2MS plus with 100 μM AS for 52~55 h. Fresh 1/2MS plus with 100 μM AS was added immediately to keep the OD600<1.0. Then the GUS activities of the transformed leaves treated by 25 and 37°C were determined. Every treatment was replicated three times and each replicate contained at least 15 seedlings.
Characterization of the potential upstream regulator of JrGRAS2
The core sequence of DOFCOREZM motif is "AAAG", and total 26 DOFCOREZM elements were found in the JrGRAS2 promoter (Additional file 2: Table S1, Additional file 1: Figure S1). Yeast one-hybrid assays were employed to identify the up-stream TFs capable of recognizing the DOFCOREZM motif. Three tandem copies of "AAAG" were cloned into pHis2 vector (pHis2-DOF) (Fig. 2a) . The Dof TFs were identified from the J. regia transcriptome and then cloned into the pGADT7-Rec2 vector to generate a cDNA library for use in yeast one-hybrid assays . The interactions between the DOFCOREZM motif and positive clones were further confirmed by examining the binding of mutated motif or promoter segments to the potential Dof TFs. I.e, the DOFCOREZM "AAAG" was mutated to "CCCA" and inserted into pHis2 (pHis2-DOF-M); JrGRAS2 promoter fragments including the DOFCOREZM motif (pHis2-DOF-S), containing the mutated DOFCOREZM motif (pHis2-DOF-M1), and excluding the DOFCOREZM motif (pHis2-DOF-M2) were all independently cloned into pHis2 ; Then the interactions between pHis2-DOF-M, or pHis2-DOF-S, or pHis2-DOF-M1, or pHis2-DOF-M2 and candidate positive clones were verified on the TDO plates with 50 mM 3-AT. The construct of p53His2 was set as a control in the yeast one-hybrid assays [42, 61].
Furthermore, above interactions were examined in tobacco seedlings by transient co-expression method [42, 43]. The DOFCOREZM motif (DOF), DOF-M, DOF-S, DOF-M1, DOF-M2 were each fused with a CaMV35S-46 minimal promoter to construct recombinants, which were further independently cloned into the pCAMBIA1301 vector to drive the GUS gene expression (reporters) (Fig. 3a) . The ORF of the screened TF-- JrDof3 was cloned into pROKII vector under the control of a 35S promoter (pROKII-JrDof3) to generate the effecter (Fig. 3a) , which was transiently co-transformed with each of the reporters in tobacco leaves using Agrobacterium-mediated transformation method, then GUS activities of the co-transformed tobacco leaves were measured to evaluate the interactions [61, 62]. Every co-transformation was replicated three times and each replicate contained at least 20 leaves. Meanwhile, the direct binding of JrDof3 to the JrGRAS2 promoter was analyzed by Chip-PCR using the JrGRAS2 promoter segment containing the DOFCOREZM motif (S), or containing the mutated DOFCOREZM motif (M1), or excluding the DOFCOREZM motif (M2). The Chip assay was performed according to instructions of ChIP Assay Kit (Beyotime Biotechnology, Shanghai, China) (http://www.beyotime.com) and the published method . All the used primers are listed in Additional file 4: Table S2.
RNA isolation and HT stress response analysis of JrGRAS2 and JrDof3
Total RNA of each sample was isolated using the CTAB method and reverse-transcribed into cDNA , which was used as the template of qRT-PCR after diluting to 1/10 of the original concentration with sterile water. The 18S rRNA was used as a reference gene . The qRT-PCR was performed in a CFX96 TouchTM Real-Time PCR Detection System (Bio-Rad Laboratories, Redmond, WA) . The 20 μL reaction mixture contained 10 μL of SYBR Green Real-time PCR Master Mix (CWBIO), 0.5 μM of each forward and reverse primer (Additional file 4: Table S2), 2 μL cDNA template (equivalent to 100 ng of total RNA). The amplification was applied using the following cycling parameters: one cycle of 94°C for 30 s, followed with 44 cycles at 94°C for 12 s, 60°C for 30 s, 72°C for 40 s, and at 81°C for 1 s plate reading. Three independent experiments were applied to ensure the reproducibility of qRT-PCR results. The relative expression levels were calculated based on the threshold cycle according to the 2-ΔΔCT method .
HT stress tolerance analysis of JrGRAS2 in transgenic Arabidopsis plants
The open reading frame (ORF) of JrGRAS2 was amplified using the primers of JrGRAS2-F/-R (Additional file 4: Table S2), which was further confirmed by sequencing. The JrGRAS2 amplified ORF fragment was digested by XbaI and KpnI and then cloned into pROKII vector under the control of a CaMV35S promoter to construct 35S::JrGRAS2. The EHA105 harboring recombinant 35S::JrGRAS2 was cultivated and used for transformation of Arabidopsis plants. Kanamycin-resistant transformed seedlings were detected by PCR, whose expression level was analyzed by qRT-PCR. Three transgenic lines with highest expression of JrGRAS2 (Line S3, S7, and S8) were chosen for further analysis.
Firstly, the seed germination ability and growth performance exposed to HT were analyzed. The seeds of WT, S3, S7, and S8 were sown on 1/2MS agar medium under 24°C or 37°C for 12 d. Then the germination rate and fresh weight were recorded, respectively. Next, the ROS accumulation was assessed. The 5-week-old plants of WT, S3, S7, and S8 grow under normal conditions were transferred to 37°C for another one-week, then the leaves were stained by Evans blue, and the corresponding EL rate, H2O2 and MDA contents were tested. Lastly, the activities of the antioxidases including CAT, POD, SOD, and GST were determined under the treatments as ROS accumulation assessment.
Transient expression analysis of JrGRAS2 to HT stress
To further confirm the HT stress response ability of JrGRAS2, the recombinant 35S::JrGRAS2 was transient transformed into walnut. The EHA105 (35S::JrGRAS2) and EHA105 (pROKII) (CK) cells were grown to OD600=0.8, then diluted to OD600=0.05 in 1/2MS liquid medium supplementing with 100 μM AS. Then the three-mouth-old J. regia leaves were transformed as the method using for pCAM-JrGRAS2-P transient transformation . The non-transformed (NT) and CK lines were used as control. The expression level of JrGRAS2 was checked to confirm the transformation. The EL rate, MDA content, SOD activity and POD activity were tested. The transcription of walnut HSP genes (JrHSP70, JrsHSP17.3, JrHSP20-1) were analyzed to understand the regulation of JrGRAS2 whether relating to HSPs. All experiments were performed three times, each replicate contained 15 seedlings.
Transcription analysis of the HSPs regulating by JrGRAS2
The HSP proteins were identified from the Arabidopsis genome online database --TAIR (The Arabidopsis Information Resource, http://www.arabidopsis.org/). Total 18 HSP genes from different subfamilies were selected, they are AtHSP70B, AtHSP70T-1, AtHSP101, AtHsp90C, AtHSP98.7, AtHSP60-2, AtHsp90.6, AtHSP60-3A, AtHSP60-3B, AtHSP17.4, AtHSP93-III, AtHSP20, AtHSP23.6, AtHSP17.6II, AtHSP83, AtHsp81.4, AtHSP21, and AtHSP18.2. Their expression levels were confirmed in JrGRAS2 transgenic Arabidopsis plants using qRT-PCR. Actin2 was used as an internal control. All the primers and gene accession number were included in Additional file 5: Table S3.
All experiments were repeated three times, all of the data were analyzed using the Statistical Package for Social Science (SPSS) (SPSS, Chicago, Illinois), the sample variability is reported as standard deviation (S.D.). The differences between the transgenic and WT lines were evaluated using Tukey’s multiple comparison test with the significance level set at p<0.05.
The current study was supported by Central University Basic Research Funds Project of China (2452016057, 2452015171), Inaugurating Program of Northwest A & F University for Doctoral Staff (2452015295), Natural Science Basic Research Project of Shaanxi Province (2018JQ3066), National Natural Science Foundation of China (31700332, 31800510), Special Financial Grant from the China Postdoctoral Science Foundation (2017T100782). The funding agency was not involved in the design of the study, collection, analysis, and interpretation of data and in writing the manuscript.
Availability of data and materials
The datasets used and/or analyzed during the current study available from the corresponding author on reasonable request.
GY wrote the paper, analyzed all the data and fund part for the experiments. XG completed the Arabidopsis transformation, promoter identification and Chip-PCR. KM did the yeast one-hybrid assay, transient co-expression analysis and tested the physiological index. DL isolated the DNA, RNA and carried out the qRT-PCR experiments. CJ and MZ analysis and interpretation part of the data. MZ and ZX fund partial for the current study. GY and ZX designed the study, and ZX inspected and re-analyzed all the data. All authors have read and approved the final version.
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