A bZIP transcription factor GhVIP1 increased drought tolerance in upland cotton

Cotton is extremely affected by severe natural stresses. Drought is one of the most serious abiotic stress that adversely influences cotton growth, productivity, and fiber quality. Previous studies indicate that basic leucine-zipper (bZIP) transcription factors are involved in the response of plants to various stresses. However, the molecular function and regulatory mechanism of GhVIP1 in response to drought stress are still unknown. In this research, GhVIP1 was cloned from a drought-tolerant variety. Expression of GhVIP1 was up-regulated in response to multiple abiotic stresses, especially under drought stress. And GhVIP1 was highly expressed in the root, stem, and 10 days post-anthesis ovule. Inhibiting the expression of GhVIP1 in cotton using the virus-induced gene silencing method resulted in higher electrical conductivity in leaves, but lower water content under drought stress compared with the WT plant. Overexpression of GhVIP1 in Arabidopsis enhanced plant drought tolerance through increasing the seed germination rate and improving the development of root. The exogenous expression of GhVIP1 up-regulated the transcription of genes associated with drought response and proline biosynthesis during drought stress in Arabidopsis. In summary, these results indicated that GhVIP1 played a positive role in plants' response to drought stress. The use of GhVIP1 via modern biotechnology might facilitate the improvement of drought tolerance in cotton cultivars.


Introduction
Along with global warming and climate change, drought has become a major severe abiotic stress to plant.It adversely influenced the whole process of plants growth and development by changing the cell membrane structure and permeability, reducing the leaf water potential and transpiration rate, inhibiting the photosynthesis, and disrupting the normal metabolism in plant.Accordingly, plants have evolved a range of complex regulatory mechanisms to cope with the harsh environmental stress of water shortage.Among them, transcriptional factors played a key role in regulating expression levels of a series downstream genes in response to drought stress.Transcription factors including WRKY, NAC, AP2, MYB, and bZIP play a crucial role in the process of plants response to drought stress (Golldack et al. 2011;Baldoni et al. 2015;Li et al. 2021).
As a paramount commercial crop, cotton is the main source of cellulosic fiber oil and biofuel.However, cotton, like other plants is extremely affected by severe natural stresses.Drought is known as one of the most serious abiotic stresses that adversely influences cotton growth, productivity, and fiber quality.To improve the drought resistance of cotton, many efforts have been made to better understand the mechanism of drought tolerance.Drought-associated candidate genes have been explored and isolated using modern biotechnologies, including whole genome sequencing (WGS) / whole genome re-sequencing (WGR), genome-wide association studies (GWAS), and bulked segregant analysis (BSA-Seq).Integrating genome modification technologies including transgenic approaches and CRISPR/Cas9 genome editing systems, drought-tolerant cotton materials were developed.Hou et al. have revealed that the genetic bases of drought tolerance through genotyping 319 upland cotton accessions.Twenty single nucleotide polymorphism (SNPs) traits and 4 candidate genes related to drought-tolerance have been identified using GWAS and RNA-seq techniques (Hou et al. 2018).Traits from natural populations formed from 200 representative cotton accessions under drought stress were investigated on 119 images from an automatic phenotyping platform, and genes related to drought resistance, such as GhRD2, GhNAC4, GhHAT22, and GhDREB2 were identified and selected by integrating digital phenotyping, GWAS analysis, and transcriptome data (Li et al. 2020).Additionally, earlier studies demonstrated that GhNAC2, GhWRKY21, GhNAC072, GbWRKY1, and GhWRKY33 play a key role in drought tolerance in cotton, which have proved that transcription factors were also significantly important in the response of cotton to drought stress (Gunapati et al. 2016;Wang et al. 2021;Mehari et al. 2021;Luo et al. 2020;Wang et al. 2019).Thus, it is feasible to improve drought tolerance in cotton by regulating the gene expression of transcription factors.
VirE2 interacting protein 1 (VIP1), is a basic leucine-zipper (bZIP) transcription factor, which was first identified in Arabidopsis (Tzfira et al. 2000).VIP1 acts as a bridge between VirE2 and nuclear importin α, it is involved in the formation of the T-DNA complex, and mediates the transportation of T-DNA in the cytoplasm to the plant nucleus (Citovsky et al. 2004;Djamei et al. 2007).Besides vital roles in Agrobacterium-mediated transformation, VIP1 is associated with other functions such as plant defense responses, sulfur utilization, starch accumulation, metal-binding, touchinduced root waving, in particular, the abiotic stress response (Wu et al. 2010;Zhang et al. 2019;Tsugama et al. 2016;Chen et al. 2016;Tsugama et al. 2018).VIP1 encodes a functional bZIP transcription factor and regulates the expression of downstream stress-related genes through binding to the VIP1 response element (VRE) in the promoters of the stress-related genes.VRE is a DNA hexamer motif, which is known as the specific binding site of the VIP protein (Pitzschke et al. 2009).Tsugama et al. have suggested that the binding of VIP1 enhances the promoter activities of CYP707A1/3 genes and is involved in the osmosensitivity signaling process in Arabidopsis.Liu et al. has found that OsbZIP81, a homolog of Arabidopsis VIP1, was largely induced by MeJA and PEG6000 treatments.OsbZIP81 positively affects the endogenous JA level via regulating the expression level of OsPIOX, which belongs to the α-linolenic acid metabolism pathway (Liu et al. 2019).A research group recently reported that BnMYB44 and BnVIP1 are candidate hub genes that contribute to drought and salt stress response in Brassica napus.The expression level of BnMYB44 and BnVIP1 were quickly and significantly induced and up-regulated under drought conditions in a stress-tolerant cultivar (Shamloo-Dashtpagerdi et al. 2018).Additionally, MYB44 promoters are activated by the VIP1 transcription factor through binding to VREs, and the expression level of MYB44 has been increased in plants overexpressing VIP1 (Pitzschke et al. 2009).Xu et al. has suggested that AtVIP1 is phosphorylated by MPK6 and responded to ABA signaling.The drought tolerance was significantly improved in transgenic plants overexpression of AtVIP1 (Xu et al. 2015).
It is clear that VIP1 as a transcriptional regulator, controls stress-related gene expression by binding to VRE and acts as key player to cope with severe abiotic and biotic stresses.However, the molecular function and regulatory mechanism of GhVIP1 in cotton especially in response to drought stress are still unknown.In this study, GhVIP1 has been isolated from a drought tolerance cotton variety and the structure, expression pattern, and hereditary character of GhVIP1 has been investigated.The molecular function of GhVIP1 has been verified in cotton and Arabidopsis using transient virus induced gene silencing (VIGS) and stable transformation methods.This research expands the knowledge of the function of GhVIP1 in response to drought and will facilitate new approaches to improve drought tolerance in cotton cultivars.

Characterization of GhVIP1 in cotton
In this study, GhVIP1 was isolated from Gossypium hirsutum cv Zhong H177, a drought-tolerant germplasm.The open reading frame (ORF) of GhVIP1 was 1 002 bp in length and encoded a protein of 333 amino acid residues.There were four nucleotide variations between the sequence of GhVIP1 from Zhong H177 (tolerant) and TM-1 (sensitive), which caused a difference of one amino acid (Additional file 1, Fig. 1a).Results of a phylogenetic analysis indicated that the VIP1 protein from other plants contained a single bZIP domain, which was the most conservative region among VIP1 proteins (Fig. 1a).The 3D structures of the conserved domains in VIP1 proteins were predicted by SWISS-MODEL online software.VIP1 proteins from different plants had conserved topology structures (Fig. 1b).Cis-regulatory elements of promoter regions played a vital role in regulating downstream gene expressions.Thus, cisregulatory elements of GhVIP1 promoter regions were predicted and results indicated that 1, 1, 5, 2, and 9 cis-elements responded to defense and stress, drought, abscisic acid, MeJA, and light, respectively.The results of topology prediction, phylogenetic analysis, and promoter analysis suggested that VIP1 proteins were evolutionarily conserved and were involved in stress and phytohormone responses.

Subcellular localization and expression pattern of GhVIP1 in different tissues and responding to stresses
The subcellular localization of a protein has a strong correlation with its function.The online prediction result from WOLFPSORT software suggested that GhVIP1 was localized in the nucleus and cytoplasm.To determine the subcellular localization of GhVIP1, the vector pBI121-GhVIP1-GFP was constructed.Results indicated that GhVIP1 was localized in the nucleus and cell membrane (Fig. 2).To improve the understanding of the important roles of GhVIP1 in cotton, the expression pattern of GhVIP1 in different tissues and in response to stress were analyzed using qRT-PCR.The results showed that GhVIP1 was highly expressed in the root, stem, and ovule at 10 days post-anthesis (DPA), and the expression levels in the leaf and ovule at 25 DPA were low (Fig. 3a).Additionally, GhVIP1 was up-regulated under cold, drought, and salt stresses compared with normal conditions.Furthermore, changes in the expression level appeared as early as the 3 h after stress treatment.The transcript of GhVIP1 was not induced under heat stress (Fig. 3b).

Functional evaluation of GhVIP1 in drought response
To investigate the function of GhVIP1 in response to drought stress in further detail, VIGS technology was used to generate GhVIP1-silenced cotton seedlings, and the PDS gene was used to monitor the VIGS efficiency.The recombinant vector of TRV2:GhVIP1 was constructed (Fig. 4a).When an albino phenotype appeared in the true leaves of cotton seedlings inoculated with Agrobacteria containing the PDS gene (TRV:PDS), the expression level of GhVIP1 was decreased in the silenced plants (TRV: GhVIP1) compared with the control (TRV:00) (Fig. 4b, c).There was no obvious phenotypic difference under normal conditions between TRV:GhVIP1 and control plants.For the silenced and control plants which were transferred to the 10% PEG6000 solution, the leaves of TRV:GhVIP1 exhibited an obvious yellow and wilting phenotype compared with the control plants (Fig. 4d).In addition, the electrical conductivity (EC) of leaves from VIGS and control plants were measured.The detached leaves from silenced lines showed higher EC values than the control under drought stress (Fig. 4e).Overall, the current results indicated that GhVIP1 might be involved in responding to drought stress in cotton.

Ectopic expression of GhVIP1 enhanced Arabidopsis tolerance to drought
Earlier studies suggested that GhVIP1 played a vital role in coping with drought stress.Transgenic Arabidopsis lines overexpressing GhVIP1 were generated by flower soaking to further investigate the drought resistant function of GhVIP1.The exogenous GhVIP1 gene was driven by 35S promoters and the kanamycin resistant gene was used as a marker for screening (Fig. 5a).After kanamycin selection and qRT-PCR analysis, two homozygous overexpression lines OE1 and OE2, with relatively higher GhVIP1 expression levels in Arabidopsis were selected (Fig. 5b).There was no obvious morphological difference between transgenic plants and wild type (Col-0) under normal conditions.The germination rate and root length of transgenic plants and WT on 1/2 MS agar media containing mannitol were measured to explore whether GhVIP1 was involved in the response to drought stress in Arabidopsis.Seeds of the two overexpression lines and WT were surface sterilized and symmetrically sown on 1/2 MS agar media with or without the addition of 200 mmol•L -1 mannitol.As shown in Fig. 5, all transgenic and WT plants were germinated and showed similar growth status on normal plates.However, the OE1 and OE2 plants exhibited better growth status and higher germination rates than that of WT plants on 1/2 MS medium supplemented with 200 mmol•L -1 mannitol (Fig. 5c).Additionally, under drought treatment, the germination rate of WT was approximately 50% of the transgenic lines (Fig. 5d).The transgenic and WT seeds were then sowed vertically on 1/2 MS medium with or without 200 mmol•L -1 mannitol to analyze root development.Length and thickness were used as a standard to measure the root development.On normal medium, there was no significant difference in the root growth.However, the roots growth of transgenic and WT plants were both inhibited under drought treatment, but the roots of transgenic lines were longer and thicker than that of the WT on 1/2 MS medium containing 200 mmol•L -1 mannitol (Fig. 6a and b).To verify the function of GhVIP1 in Arabidopsis drought resistance during the vegetative growth stage, transgenic and WT seeds were sown in soil.Plant seedlings of similar growth status were selected and irrigated with 15% PEG6000 to simulate drought conditions.The results showed that after 10 days of the drought treatment, the leaves of WT plants began to wilt and were less green.whereas the growth of Arabidopsis plants overexpressing GhVIP1 were less affected (Fig. 6c).These results indicated that GhVIP1 could enhance drought tolerance by increasing seed germination rate and improving root development.

Overexpression of GhVIP1 in transgenic Arabidopsis regulated drought-related gene expression
To explore a possible mechanism for GhVIP1-mediated tolerance to drought in transgenic plants, the expression level of drought-related genes including P5CS1, P5CS, DREB1, RAB18, RAD29, and COR15A were measured under drought stress using qRT-PCR.Results indicated that P5CS1 and P5CS which are key enzymes in the proline biosynthetic pathway were significantly upregulated under drought stress in transgenic plants compared with WT.The expression level of P5CS1 increased gradually and reached the maximum at 24 h, whereas that of P5CS increased rapidly at the beginning of drought stress (Fig. 7).The transcript of RAB18 was induced more strongly at 6 h and 12 h after drought stress in transgenic plants than in WT, whereas the expression pattern of RAB18 was the opposite at 24 h after drought stress.The expression level of DREB1, RAD29, and COR15A was induced more remarkablely at 3 h after drought stress in transgenic plants than in WT, whereas the transcription level of genes were decreased after 12 h under drought condition (Fig. 7).Overall, GhVIP1 might be involved in the coping mechanism of plant to drought stress by regulating the expression pattern of genes related to the proline biosynthetic pathway.

Discussion
The bZIP family of transcription factors comprises one of the largest transcription factor families in plants and is evolutionarily conserved in eukaryotic organisms (Droge-Laser et al. 2018;Ye et al. 2022).Earlier studies indicated that a total of 197 bZIP transcription factor members were identified in G. hirsutum genome, and could be divided into 13 subfamilies through phylogenetic analysis based on conserved motifs and gene structures (Zhang et al. 2022a).The bZIP transcription factors are involved in a plethora of functions in various biological processes, especially in response to abiotic stresses (Wang et al. 2020).Zhang et al. has cloned and characterized the bZIP transcription factor GhABF3, and has suggested that the gene is involved in the drought and salt stress response in plants.Overexpression of the GhABF3 gene has up-regulated the RD29B, RAD18, and CHS genes, increased root length, reduced the degree of cellular oxidation, and decreased leaf water loss and wilting, which has resulted in the improvement of drought and salinity tolerance in cotton and Arabidopsis (Zhang et al. 2022b).GhABF2 has also been induced by drought and ABA treatment and the overexpression of GhABF2 in cotton has enhanced plant drought and salt tolerance  ABA and MeJA are important phytohormones, play a key role in responding to various stresses.Several genes that participate in the response to stress by plants regulating the expression of genes related to the ABA or MeJA pathways.It has been reported that the expression of VIP1 genes was induced by ABA and MeJA.The transcription levels of OsbZIP81.1 and OsbZIP81.1,which are two homologs of AtVIP1 in rice, are strongly induced by MeJA, PEG6000, and Agrobacterium infection (Liu et al. 2019).In this study, GhVIP1 has been rapidly and significantly induced by cold, drought, and salt treatment.The margin in the increase of GhVIP1relative expression level is not huge, which consists with previous studies.It might be that GhVIP1, as a functional transcription factor, strongly enhances the expression level of multiple genes which harbor several VRE motifs, but does not play a direct role.GhVIP1 was not remarkablely induced by treatment with ABA in cotton probably because there were differences in the expression patterns of VIP1 among plants.
The VIP1 protein acts as a transcriptional factor and regulates downstream genes mainly through binding to VREs at promoters.VRE contains a DNA hexamer motif and the combination of VIP1-VRE significantly enhances the expression level of genes with promoters that harbor several VRE motifs (Lacroix and Citovsky 2013).Earlier studies verified that promoters of the Trxh8 and MYB44 genes have six and three copies of VRE, respectively, and their expression levels have been activated by VIP1 in a VRE-dependent manner in Arabidopsis (Pitzschke et al. 2009)  were directly regulated by OsbZIP81.1,respectively (Liu et al. 2019).In this study, the relationship between GhVIP1 and genes involved in the drought response including P5CS1, P5CS, DREB1, RAB18, RAD29, and COR15A has been analyzed using qRT-PCR.Although the expression pattern of the genes mentioned above was not identical, all of the genes have been detected a rapidly induction in transgenic plants under drought stress.Additionally, the binding motifs of GhVIP1 and the evolutionary conservation in binding motifs among bZIP transcriptional factors in cotton have not been well studied.Research of transcription factor-bound cis-acting elements in the bZIP transcriptional factor has important impact and provides new insights into further studies of bZIP family in plants.
The growth and production of cotton are adversely affected by drought stress and many efforts have been made to manage the threat of drought stress.Previous studies have indicated that drought tolerance is a complicated process that included stress sensing and multiple stress responses (Mahmood et al. 2019).The stress signaling pathway involved in the cotton drought response mainly includes the mitogen-activated protein kinase (MAPK) signaling pathway, Ca 2+ signaling pathway, and phytohormone-mediated signaling pathway (Wang et al. 2016;He et al. 2013;Luo et al. 2020).Several stress responses including morpho-physiological responses, biochemical, and cellular responses, and antioxidant defense are known to minimize or reduce the damage caused by drought (Singh et al. 2022).Li et al. have demonstrated that stomatal movement including the closure speed, length, and width of stomata are involved in plant tolerance to drought stress (Li et al. 2022).Overexpression of SNAC1 remarkablely improved root development including root biomass and root length in cotton which results in increased tolerance to drought in cotton (Liu et al. 2014).In this study, the roots of transgenic plants overexpressing GhVIP1 are obviously longer and thicker than that of the WT grown in 1/2 MS medium containing 200 mmol•L -1 mannitol, which was potentially important in the response to drought stress.
Results have indicated that P5CS1 and P5CS genes are significantly upregulated under drought stress in transgenic plants compared with WT.P5CS1 and P5CS which are rate-limiting enzymes in the proline biosynthetic pathway.Proline accumulation is a major metabolic adaptation of plants in response to multiple environmental stresses (Feng et al. 2016;Shrestha et al.Fig. 7 The expression pattern of drought tolerance associated genes in GhVIP1 overexpression plants under drought stress.The expression data of 6 h, 12 h, 24 h, 48 h were normalized to that of 0 h."**" and "***" represented a significant difference between WT and GhVIP1 overexpression plants at 0.01 and 0.001 probability level by t-test, respectively 2022).Increasing proline accumulation and the application of exogenous proline has been verified to improve plant drought tolerance (Ashraf and Foolad 2007).Chen et al. have indicated that overexpression of the FRIGIDA gene improves drought tolerance by up-regulating P5CS1 expression level and proline accumulation under drought stress (Chen et al. 2018).Li et al. has suggested that OsERF71 plays a positive role in drought-induced proline biosynthesis by increasing the expression level of OsP5CS1 and OsP5CS2 genes which enhanced the tolerance of rice to drought (Li et al. 2018).Taken together, we propose that GhVIP1 improves cotton drought tolerance by up-regulating the expression level of genes involved in proline biosynthesis and by increasing the length and biomass of roots under drought stress.These findings have broadened our knowledge of the function of GhVIP1 involved in cotton drought tolerance.However, the molecular mechanism and regulation relationship underlying GhVIP1 and genes associated with drought tolerance need further characterization.

Conclusion
In this study, the data has suggested that GhVIP1 plays a positive role in the regulation of drought tolerance in cotton.GhVIP1 expression has induced by various abiotic stresses and the GhVIP1 protein is located in the nucleus and cell membrane.Silencing of GhVIP1 in cotton reduces plant drought tolerance and GhVIP1 overexpressing Arabidopsis lines exhibites improved tolerance to drought.GhVIP1 participates in the drought response by increasing the length and biomass of root in transgenic plants, and by up-regulating the expression level of genes involved in proline biosynthesis.

Plant materials and treatment conditions
Tetraploid upland cotton Zhong H177 which is known as a drought-tolerant cultivar, and TM-1 were used for gene cloning.The seeds were soaked overnight in water and cultured on absorbent paper at 37 °C for 24 h in the dark.The germinated seeds were planted in nutrient soil and grown in incubators under conditions of 28 °C (day) /25 °C (night) with a light cycle of 16 h/8 h.Three true-leaf stage cotton seedlings were selected and treated with drought stress, in which 15% PEG 6000 and 200 mmol•L -1 NaCl were used for simulating drought and salt environment, respectively.For cold and hot treatment, cotton seedlings were transferred to a chilling chamber ( 4 °C) and hot chamber (37 °C), respectively.Normal treatment was applied on the control.The leaves of plant seedings were harvested at 0 h, 1 h, 3 h, 6 h, 12 h, 24 h after stress treatment and frozen in liquid nitrogen.The treatment had at least three biological repeats and each repeat had more than five plants.

Subcellular localization of GhVIP1
To predict the subcellular localization of GhVIP1, the WOLFPSORT online software (https:// wolfp sort.hgc.jp) was used.The pBI121 vector containing the GhVIP1 gene (without the stop codon) was used for transient expression and was transformed to tobacco leaf cells by the Agrobacterium infiltration method.The empty vector was used as a negative control.The fluorescence signals of subcellular localization were observed using a laser confocal scanning microscope Olympus FV1200 (Olympus, Tokyo, Japan) with the excitation and emission wavelength of 488 nm and 510 nm, respectively.

Agrobacterium-mediated virus-induced gene silencing analysis
A 272 bp GhVIP1 fragment was amplified and cloned into TRV2 vectors, forming the recombinant vector of TRV:GhVIP1 through a ClonExpress II One Step Cloning Kit (Vazyme, Nanjing, China).Then recombinant vector of TRV2:GhVIP1 and TRV2:PDS, as well as the empty vector were transformed into an Agrobacterium tumefaciens strain GV3101 using the freeze thaw method.Activated Agrobacterium containing TRV2 vectors and the TRV1 vector were mixed in a 1:1 ratio, and then the mixture were infiltrated into the cotyledons of Zhong H177 seedlings.The silence efficiencies of VIGS were detected by qRT-PCR when the TRV2:PDS plants exhibited an albino phenotype.The target gene-silenced cotton plants were treated with drought stress (15% PEG).VIGS experiments were repeated at least three times and each repeat used more than 15 plants.

Transformation of Arabidopsis
The full-length ORF of GhVIP1 was inserted into the binary vector pBI121 containing the cauliflower mosaic virus (CaMV) 35S promoter to construct 35S:GhVIP1.An Agrobacterium (Strain GV3101) harboring the recombinant construct vector was transformed into Arabidopsis (Colombia-0; WT) via the floral dip method.The seeds of transformants were first screened on 1/2 MS medium with 50 mg•L -1 kanamycin.Then PCR was used to verify the transformants and qRT-PCR was applied to detect the expression level of the exogenous GhVIP1 gene.Descendants from self-fertilization whose segregation ratio consisted with the genetic laws of Mendel and with correct expression of the exogenous GhVIP1 were efficiently selected to produce homozygous T3 lines for futher experiments.Two independent homozygous lines of transgenic plants were used to analyze growth and morphological differences.For the germination assay, seeds of transgenic lines and WT were sterilized firstly by 70% ethanol for 1 min and then by 10% NaClO for 5 min.Sterilized seeds were washed three times using sterile water and then spread on the 1/2 MS medium with or without 200 mmol•L -1 mannitol at 25 °C day/23 °C night by 16 h/8 h light-dark.After 10 days, the growth status and germination rate of transgenic and WT plant under normal or simulated drought stress conditions were calculated and determined.For root lengths measurement, the seed sterilization method and medium formula were the same as described previously.The seeds were sowed vertically on normal and drought stress media.The length and thickness of roots were observed and photographed.To study drought stress response during the vegetative growth stage, seeds of transgenic Arabidopsis and the control were directly sown in the nutrient soil.The drought treatment was similar to that of cotton seedlings described previously.

Fig. 2
Fig. 2 Subcellular localization of GhVIP1 in tobacco leaves

Fig. 3
Fig. 3 Expression pattern of GhVIP1 gene in different tissues and under different stresses.a Analysis of GhVIP1 expression in different tissues.b Analysis of GhVIP1 expression under cold, heat, PEG, and NaCl treatment.0 h was the control and "*" represented a significant difference at 0.05 probability level by t-test

Fig. 4
Fig. 4 Silencing of GhVIP1 reduced the tolerance to drought stress in cotton.a Vector structures of TRV2:GhVIP1.b Albino phenotype of TRV:PDS.c Detection of silencing efficiency.d Drought tolerance assay of GhVIP1-silenced seedlings compared with the control.e Relative electrical conductivities analysis on the detached leaves of TRV:00 and TRV:GhVIP1 cotton seedlings under drought stress

Fig. 5
Fig. 5 Verification and function analysis of GhVIP1 transgenic plants.a Construction of overexpression vector.b The expression level of exogenous GhVIP1 gene in transgenic plants were detected by qRT-PCR.WT was used as control and "**" represented a significant difference at 0.01 probability level.c Germination of GhVIP1 overexpressed Arabidopsis and WT plant under drought stress.d Statistic analysis of root length of transgenic plants and WT on 1/2 MS agar media with or without 200 mM mannitol."**" represented a significant difference at the 0.01 probability level . Liu et al. have discovered a novel binding motif of OsVIP1 via ChIP-Seq, named as OVRE.The expression level of OsLOX5, OsHI-LOX, OsAOC, and OsPIOX genes

Fig. 6
Fig. 6 GhVIP1 overexpression Arabidopsis increased the root length and drought tolerance.a Transgenic plants overexpressing GhVIP1 and WT plants on 1/2MS with or without 200 mmol•L -1 mannitol.b Analysis of root length of transgenic plants and WT under normal condition and drought stress.c Phenotypic comparison of plants with ectopic expression of GhVIP1 and WT Arabidopsis under 10% PEG treatment