- Research article
- Open Access
GaMYB85, an R2R3 MYB gene, in transgenic Arabidopsis plays an important role in drought tolerance
BMC Plant Biology volume 17, Article number: 142 (2017)
MYB transcription factors (TFs) are one of the largest families of TFs in higher plants and are involved in diverse biological, functional, and structural processes. Previously, very few functional validation studies on R2R3 MYB have been conducted in cotton in response to abiotic stresses. In the current study, GaMYB85, a cotton R2R3 MYB TF, was ectopically expressed in Arabidopsis thaliana (Col-0) and was functionally characterized by overexpression in transgenic plants.
The in-silico analysis of GaMYB85 shows the presence of a SANT domain with a conserved R2R3 MYB imperfect repeat. The GaMYB85 protein has a 257-amino acid sequence, a molecular weight of 24.91 kD, and an isoelectric point of 5.58. Arabidopsis plants overexpressing GaMYB85 exhibited a higher seed germination rate in response to mannitol and salt stress, and higher drought avoidance efficiency than wild-type plants upon water deprivation. These plants had notably higher levels of free proline and chlorophyll with subsequent lower water loss rates and higher relative water content. Germination of GaMYB85 transgenics was more sensitive to abscisic acid (ABA) and extremely liable to ABA-induced inhibition of primary root elongation. Moreover, when subjected to treatment with different concentrations of ABA, transgenic plants with ectopically expressed GaMYB85 showed reduced stomatal density, with greater stomatal size and lower stomatal opening rates than those in wild-type plants. Ectopic expression of GaMYB85 led to enhanced transcript levels of stress-related marker genes such as RD22, ADH1, RD29A, P5CS, and ABI5.
Our results indicate previously unknown roles of GaMYB85, showing that it confers good drought, salt, and freezing tolerance, most probably via an ABA-induced pathway. These findings can potentially be exploited to develop improved abiotic stress tolerance in cotton plants.
Environmental factors, particularly drought stress, severely limit the production and distribution of many important agronomic crops worldwide . In plants, different types of transcription factors (TFs), such as bZIP, NAC, AP2, WRKY, and MYB, control plant biological processes by modulating the initiation rate of target genes with the combined activation of a DNA binding domain, a nuclear localization signal, a transcription activation domain, and oligomerization sites in response to biotic or abiotic stresses . MYB TFs were first recognized as oncogenes in animals; however, it has subsequently been found that MYB genes occur more widely in plants than in animals and fungi [3, 4]. Following the discovery of the first plant MYB gene in maize (Zea mays) , large numbers of MYB proteins, particularly R2R3 MYBs, have been extensively identified and characterized in different plant species, including Arabidopsis, apple, grape, maize, petunia, and snapdragon . Furthermore, R2R3 MYBs are known to control abundant plant biological processes, such as hormone signal transduction, organ development, cell cycle progression, cellular morphogenesis, secondary metabolism, and stress responses [7, 8]. More recently, genome-wide studies of Gossypium raimondii have revealed 205 putative R2R3 MYB genes, which is a greater number than reported in any other dicot or monocot .
Structurally, MYB proteins have a highly conserved MYB or DBD (DNA-binding domain), located at the N terminus, which is well conserved across all eukaryotes, whereas the diverse C termini act as a trans-acting domain (TAD) that regulates a broad range of functions in MYB proteins [10, 11]. Moreover, each MYB repeat contains 52 amino acid residues with regularly spaced triplet tryptophan residues, which form a hydrophobic core structure. The MYB repeat structure is composed of three α-helices. Two helices form the HTH (helix-turn-helix) structure and contribute to the binding of target genes to the promoter region, whereas the third helix participates in DNA recognition [12, 13]. On the basis of their DNA-binding domain sequential repeats, MYB proteins are grouped into four types; MYB1-R, R2R3-MYB, R1R2R3-MYB (MYB3R), and 4R–MYB . However, to improve drought tolerance in the relevant crops, mining of new MYB R2R3 TFs by functional genomics and comparative genomics studies is a promising strategy, as it is the largest family of MYB proteins of higher plants and well known to be involved in specific diverse biological, functional, and structural processes.
The phytohormone abscisic acid (ABA) has numerous functions, such as in seed germination inhibition and dormancy maintenance, stomatal regulation, flowering time, and adaptations to drought, cold, and salt stresses . ABA is known to induce dehydration-responsive genes, and thus on encountering drought stress, elevated levels of ABA stimulate cis-acting and trans-acting factors, which in turn up-regulate the ABA-induced expression of MYB, NAC, WRKY, and bZIP TF genes [16,17,18,19], thereby contributing to the relief of stress conditions . Many ABA-inducible genes contain a cis-element (ABRE; ACGTGG/TC), whereas dehydration and low temperature stress-inducible genes contain a different cis-element (DRE; TACCGACAT). Both these elements play important roles in stress management via ABA-dependent and -independent signal transduction cascades [15, 21]. Moreover, MYC/MYB recognition sequences are a pre-requisite for transcript regulation of RD22 and ADH1, which is induced by high ABA levels in Arabidopsis under drought stress . In addition, different R2R3 MYB genes (AtMYB44, AtMYB15, AtMYB60, AtMYB96, AtMYB61, and GbMYB5) have been shown to be involved in stomatal regulation via ABA in response to dehydration [23,24,25]. R2R3 MYB TFs are implicated in diverse plant responses to abiotic stress conditions. For example, the AtMYB102 protein is reported to be an important component that integrates wounding, osmotic stress, and ABA transduction pathways in transgenic Arabidopsis . Similarly, overexpression studies on R2R3 MdSIMB1 , OsMYB2 , GmMYBJ1 , GmMYBJ2 , GbMYB5 , GmMYB76  and SbMYB8 , have shown improved drought, salt, and cold tolerance in transgenic plants.
Cotton is an important textile fiber and oil seed crop ; however, the repercussions of climate change, particularly drought stress, are severely limiting its production globally . Our laboratory previously released Gossypium arboreum sequencing data  and RNA-seq studies have revealed hormone crosstalk, whereby MYB TFs are implicated in modifying plant responses toward drought and NaCl stresses in different tissues . Thus, in view of the current scenario, we ectopically expressed a novel G. arboreum R2R3 MYB gene, designated GaMYB85, in Arabidopsis to study its role under drought, salt, and freezing stress conditions. Collectively, our results suggest that the GaMYB85 gene confers good drought tolerance in overexpressing transgenic Arabidopsis plants, which can potentially be employed in future cotton crop improvement.
GaMYB85 characterization and phylogenetic analysis
Previously, our mRNA-seq studies of G. arboreum showed multiple hormone crosstalk and tissue-selective signaling; moreover, MYB transcription factors are implicated in modifying cotton plant responses toward PEG and NaCl stresses in leaf, stem, and root . Therefore, characterization of a novel gene, GaMYB85, was performed in transgenic Arabidopsis plants subjected to drought and salt stresses. The full-length CDS of GaMYB85 is 771 bp long, and codes for a protein containing 257 amino acids with an expected molecular weight of 24.91 kD and a theoretical isoelectric point of 5.58 (http://web.expasy.org). Performing SMART analysis (available online at http://smart.embl-heidelberg.de/), the deduced 257-residue polypeptide was determined to contain a SANT domain between amino acids 38 and 86. The secondary structure of GaMYB85 includes 19.53% alpha helix, 19.53% extending chain, and 60.94% random coil sequences. GaMYB85 alignment results between cDNA and genomic sequence retrieved from the cotton genome database revealed that the gene contains no introns (Additional file 1), and is located on chromosome 13 with a cotton ID number of cotton_A_21601. The deduced GaMYB85 protein shares a high amino acid sequence homology with AtMYB85 (At4g22680). Overexpression of this protein in Arabidopsis resulted in the ectopic deposition of lignin in epidermal and cortical cells of the stem , and it was thus designated as GaMYB85 in further studies. Multiple sequence alignment revealed high similarity between GaMYB85 and retrieved R2R3 protein homologs of various dicots and monocots, including Gossypium hirsutum (98%), Nicotiana tabacum (82%), Arabidopsis thaliana (79%), Theobroma cacao (78%), Zea mays (84%), Hordeum vulgare (80%), Oryza sativa (70%), Triticum aestivum (66%), and Vitis vinifera (61%), which are annotated as predicted, putative, and hypothetical, and thus their functions are still unknown. However, they show the presence of conserved R2 and R3 domains in the MYB gene (http://www.ebi.ac.uk/Tools/msa/muscle/) (Fig. 1a). Moreover, in the phylogenetic tree we constructed, we also included some R2R3 MYB genes with known functions, which confer enhanced tolerance to multiple abiotic stresses. GaMYB85 shared high similarity and clustered together with its homologs from G. hirsutum, V. vinifera, and T. cacao, which indicates that they might have originated from the same common ancestor. Therefore, these results suggest that GaMYB85 is a novel gene that confers enhanced drought tolerance (Fig. 1b). LcMYB1, which has a single conservered SANT domain, belongs to a MYB-related protein, and was used as an out-group in the tree.
Overexpression of 35S:GaMYB85 in plants confers ABA hypersensitivity for seed germination and root elongation
In order to gain an understanding of the possible roles of GaMYB85 during germination and post-germination stages in response to abiotic stresses, this gene was ectopically expressed in Arabidopsis thaliana (Col-0) plants using the floral dip method. T2 seeds were selected on BASTA agar plates, and subsequently the surviving to dead plant ratio was determined (Additional files 2 and 3). Ten segregating lines with a correct segregation ratio of 3:1 were selected and transcript patterns were subsequently monitored by qRT-PCR (Fig. 2b and Additional file 5). Three lines with high gene transcript levels were selected and screened on selective media until we obtained homozygous lines. The T3 transgenic lines L3, L4, and L7 were selected for further analysis.
To examine the ABA sensitivity of transgenic plants containing ectopically expressed 35S:GaMYB85, the seeds of L3, L4, and L7 lines and WT plants were grown directly on medium containing different concentrations of ABA (0, 0.3, 0.5, 1, 2, and 5 μM), and the germination rates of these were compared. In a primary root length elongation assay, the 35S:GaMYB85 lines were more susceptible to ABA (Fig. 3a and b) than was the WT, which indicates that ABA might be involved in the root development process, and also strengthens speculation that 35S:GaMYB85 is regulated in an ABA-dependent manner. The presence of exogenous ABA had a more pronounced effect on the germination rates of 35S:GaMYB85 lines (L3, L4, and L7) than on that of the WT (Fig. 3c). Only 25% of the seeds of the 35S:GaMYB85 lines (L3, L4, and L7) were able to germinate on 2 μM ABA MS, as against 50% germination for the WT. Furthermore, a detailed time course experiment was conducted on 1 μM ABA (Fig. 3d), in which the seeds of 35S:GaMYB85 lines showed more delayed germination rates than the WT, starting from the 4th to 8th day after the onset of germination.
Overexpression of 35S:GaMYB85 in plants confers enhanced salt and osmotic tolerance
For further clarification of the effects of NaCl stress on 35S:GaMYB85 plants, seed germination and post-germination growth were monitored. The results revealed 100% germination rates for control and test seeds that were grown in control MS medium. In contrast, the germination rates of 35S:GaMYB85 lines (L3, L4, and L7) were significantly higher than those of the WT on NaCl medium (50, 100, 125, and 150 mM) in a dose-dependent manner. Moreover, these plants had higher fresh weights than WT plants, which turned yellow and produced a proportion of unviable seeds (Fig. 4a, b, and c). Primary root growth is an important indicator of plant tolerance to various stress responses, and 35S:GaMYB85 transgenic seedlings showed longer roots and had greener broader rosettes than did the control when raised on 100 mM NaCl medium (Fig. 4d and e). Furthermore, compared with the WT, the germination rate and fresh weight of 35S:GaMYB85-expressing plants were significantly higher, and growth performance was improved under 300 mM mannitol stress for 10 d (Fig. 5a, b, and c). Moreover, a root length assay on mannitol also revealed a significant difference in transgenic line root length growth on 200 and 300 mM mannitol medium from that in the WT (Fig. 5d and e). These significantly higher germination rates on simulated salt and mannitol stressed medium indicate that ectopic expression of GaMYB85 in Arabidopsis confers enhanced salt and osmotic tolerance during pre- and post-seed germination stages.
Plants with GaMYB85 overexpression show enhanced tolerance under drought and freezing stress
MYB TFs have been implicated in diverse plant responses to abiotic stress conditions . For a drought assay, 7-d-old transgenic and WT seedlings were transplanted to well-hydrated soil, and then 2 weeks later, grown L3, L4, and L7 plants were subjected to drought stress. The WT plants showed lower recovery rates of 35% along with severe drought symptoms, such as leaf rolling, shrinkage, and delayed growth, when compared with the 66.66%, 77.8%, and 70% recovery rates of GaMYB85 transgenic plants (L3, L4, and L7, respectively) following re-watering for 3 d (Fig. 6a and b). In accordance with these results, the water loss rate, which is an important indicator of drought stress evaluation, was significantly lower for transgenic lines when excised leaf weights were monitored over a 0- to 7-h time interval (Fig. 6c). The relative water content (RWC) in detached leaves of L3, L4, and L7 was approximately 71%, 81.9%, and 79.9%, respectively, whereas the RWC for WT decreased by up to 55% (Fig. 6d). Subsequently, proline and chlorophyll content were evaluated in non-stressed and drought-stressed samples. The free proline content in GaMYB85-expressing plants was higher under both normal and drought stress conditions. The proline content in overexpressing L3, L4, and L7 plants was significantly higher (19.8, 27.5, and 20.7 μg/g, respectively) than that in the WT (almost 9 μg/g) under drought stress (Fig. 6e and f). In addition, the total chlorophyll content under the non-stressed condition was nearly the same in WT and overexpressing L3, L4, and L7 plants. However, under drought stress, the total chlorophyll content of GaMYB85 plants was higher than that in WT plants. When 3-week-old Arabidopsis lines (L3, L4, and L7) ectopically expressing GaMYB85 and WT plants were exposed to a − 10 °C treatment for 3 h, and subsequently revived in a 22 ± 1 °C growth room, the plants ectopically expressing GaMYB85 showed improved recovery rates of 55.55%, 75%, and 69.44%, respectively. The adverse effect of freezing stress was more pronounced in the WT plants, which showed only 34% survival after 1 week of growth in the 22 ± 1 °C growth room (Fig. 7a and b). Overall, these results indicate that ectopically expressed GaMYB85 in Arabidopsis plays an important role under drought and freezing stresses.
Reduced stomatal density, increased stomatal response, and increased stomatal size in GaMYB85 plants
ABA production under abiotic stresses is directed to increase the sensitivity of stomatal closure, and thus to gain insight into this process, we examined the effects of ABA treatment on the stomatal opening of excised leaves of GaMYB85 plants (Fig. 8a). When different concentrations of ABA (5 μM and 10 μM) were added to a stomata opening solution, stomatal opening was reduced, as ABA induces stomatal closure. Excised leaves of GaMYB85 lines (L3, L4, and L7) treated with 5 μM ABA showed reduced stomatal opening rates of 40%–56%, which was further reduced to approximately 13.3%–23.3% under 10 μM ABA treatments. In contrast, WT plants had markedly higher stomatal opening rates of 73% and 50% under 5 and 10 μM ABA treatments, respectively (Fig. 8b). Moreover, WT stomatal density was also notably higher, at more than 127 per mm2, than with 96, 111, and 112 per mm2 for L3, L4, and L7, respectively (Fig. 8c and d). However, stomatal size (length to width dimensions) in L3, L4, and L7 was distinctly higher at 21–25 μm by 7–8.6 μm when compared with the 19 μm by 6.05 μm for the WT, as shown in Fig. 8e. Hence, GaMYB85 reduced stomatal density and reduced stomatal opening, resulting in rapid ABA-induced stomata closure, which subsequently minimized water loss rates and led to improved drought tolerance.
Transcript analysis of abiotic stress-responsive marker genes
As Arabidopsis thaliana plants with constitutive overexpression of 35S:GaMYB85 have ABA-dependent enhanced drought tolerance, in addition to increased stomatal closure upon ABA treatment, it would be of interest to gain a further understanding of how GaMYB85 affects and responds to ABA stress-responsive and signaling-related genes. To this end, eight abiotic stress-responsive genes (RD22, RD29A, RD29B, P5CS, COR15A, CBF, ADH, and Rab18) and two ABA signaling genes (ABI5 and ABI3) were selected and studied. The expression levels of five stress-responsive genes (RD29B, COR15A, CBF, Rab18, and ABI3) were nearly the same in both transgenic and WT plants in ABA-treated samples (data not shown here). However, the expression levels of five genes (RD22, RD29A, P5CS, ADH1, and ABI5) were significantly and clearly higher in L3, L4, and L7 than in the WT when treated with 100 μM ABA for 6 h (Fig. 9a-e). Thus, in response to ABA treatment, the transcript levels of ABA-induced stress marker genes may positively contribute to the improved drought stress tolerance of GaMYB85 plants.
Drought stress is a worldwide dilemma that has severely affected the annual production of cotton crops. Transcription factors are well known to participate in the maintenance of plant homeostasis in response to various biotic and abiotic factors. MYB TFs, particularly R2R3 MYBs, have been widely studied in different plant species, but to date few of these genes have been functionally validated for cotton. On the basis of diploid cotton A sequencing data , a new candidate cloned R2R3 MYB gene, designated GaMYB85, was selected and ectopically expressed in Arabidopsis thaliana, and three overexpressing lines (L3, L4, and L7) were successfully generated and functionally validated for drought stress. The amino acid sequence of GaMYB85 was predicted to contain a conservered SANT-DBD and clusters phylogenetically with R2R3 MYB proteins from other monocots and dicots, indicating that the R2R3 MYB proteins that group together may retain an identical function based on high sequence similarity. Some R2R3 MYBs with a known role in drought response were also included in a tree analysis (Additional file 2). These share a high similarity with GaMYB85 but cluster in different groups, which indicates that they might have a different number of SANT domains. Accordingly, these findings suggest that GaMYB85 is a novel R2R3 MYB gene with a SANT-DBD domain.
Environmental stimuli like drought and salt stresses specifically initiate ABA production, which induces stomatal closure, contributing to strong and healthy roots and plants with efficient stomatal regulation and water-retaining abilities [38, 39]. Furthermore, drought-tolerant plants have higher endogenous proline content, reduced water loss rates, and improved relative water content, which enhance the response potential of transgenic plants against stress. Thus, to evaluate and dissect the possible molecular mechanisms and physiological roles underlying plant tolerance, we generated transgenic Arabidopsis that ectopically expressed GaMYB85. The important finding is that 35S:GaMYB85 lines have normal growth with respect to the WT, which is in contrast to previous studies in which transgenic overexpressing plants showed stunted growth and poor seed germination rates [40, 41].
In plants, turgor regulation plays an important role in the management of low water potential for normal seed germination rates under abiotic stress conditions. Thus, the observation that our 35S:GaMYB85 plants had higher germination rates when subjected to 300 mM mannitol and 150 mM NaCl treatments indicated that they have a general osmotic stress tolerance. The adverse effects of salt on plant growth can either result in osmotic stress or specific ion toxicity. The osmotic stress phase is attributable to dehydration or the presence of salt in the external solution, but specific ion toxicity is a consequence of salt accumulation in the transpiring leaves. Moreover, seeds germination rates are dependent on water movement into the seeds, whereas exposure to salinity causes leaf cells to lose water, which is attributed to reduced turgor pressure or decreased cell wall expansion [42,43,44]. These results are in accordance with the functions of AtMYB102, AtMYB41, and GmMYBJ2, which have been demonstrated to confer improved drought tolerance in response to ABA-dependent osmotic and NaCl stresses [3, 26, 30]. As elevated levels of salt can interfere with the normal molecular functioning of plants , 35S:GaMYB85 transgenic plants might have coped with this situation via ion homeostasis mechanisms, i.e., Na+ ion extrusion, Na+ ion compartmentalization, and Na+ ion reabsorption [46,47,48]. The roots of plants are in direct contact with the soil and more sensitive to Na+ ion stress, and thus provide important clues regarding normal plant growth . Thus, 35S:GaMYB85 plants show a dose-dependent increase in root length growth upon salt treatment when compared with WT plants, but as transgenic plants show good fresh weight it implies that ionic stress was manifested. Furthermore, the primary root growth of seedlings was significantly decreased in WT plants growing on 200 and 300 mM mannitol MS, which clearly demonstrates the high osmotic tolerance exhibited by the 35S:GaMYB85 plants [50, 51]. As ABA hypersensitivity and insensitivity of seeds can occur during germination and post-germination stages under water deficit stress, our 35S:GaMYB85 plants were confirmed to have enhanced sensitivity to ABA both at the germinating and post-germinating stages, along with hypersensitivity to ABA inhibition of root elongation [52, 53] as shown in Fig. 3b and c. It is considered that ABA dependence might up-regulate the growth of roots and might be the major route by which 35S:GaMYB85 mediates its role in drought, salt, and cold stress signaling pathways [54, 55].
Constitutive overexpression of 35S:GaMYB85 in plants also resulted in better drought tolerance than in WT plants, which is further supported by the phenotypic and physiological changes that occur in these plants, such as decreased water loss rates and higher RWC. These results are consistent with the functional studies on GmMYBJ2 and TaMYB19, which have been reported to be associated with good drought tolerance ability [30, 56]. An evaluation of water loss rates and RWC is imperative to elucidate drought avoidance mechanisms and indicates a balance between water availability and transpiration rates through the stomatal apertures of transgenic plants [57, 58]. 35S:GaMYB85 plants showed slower and lower rates of water losses with higher RWC capacity than WT plants (Fig. 6c and d), which is corroborated by recent reports on the R2R3 MYBs GmMYBJ1 and OsMYB48–1 [29, 59]. The total chlorophyll content of plants is linked to the physiological and transpiration efficiency of the photosynthetic machinery , whereas the osmoprotective molecule proline is critical for maintaining cell membrane stability, and also contributes to balancing osmotic pressure and retaining the membrane integrity of plants subjected to abiotic stresses . In 35S:GaMYB85 plants, the chlorophyll and proline contents were significantly higher than those in WT plants (Fig. 6e and f), which suggests that endogenous proline levels contribute to the alleviation of water deficit stress and protect the photosynthetic apparatus from unfavorable toxic byproducts that have lethal effects on plant cells, and thereby confer drought tolerance. Interestingly, the proline levels in 35S:GaMYB85 transgenic plants are higher, even under normal condition, which suggests that this R2R3 MYB protein might specifically protect plants and confer drought tolerance via the integrated role of proline as an important osmoprotectant. Consequently, water deficit treatment indicates that drought avoidance is not only controlled by osmotic signaling but also depends on ABA-induced regulation of stomatal movement. To confirm this supposition, we examined various stomatal parameters to determine the possible roles of 35S:GaMYB85 plants in attaining good drought tolerance. In our study, 35S:GaMYB85 plants were revealed to have greater stomatal size, lower stomatal densities, and lower rates of stomatal opening than those of WT plants in response to exogenous ABA (Fig. 8b–e). These results corroborate the findings of previous studies on 35S:HDG11-transformed tobacco, which has reduced stomatal densities but increased stomatal size , and are in contrast to GbMYB5 transgenic tobacco plants, which have reduced stomatal size but the same stomatal density . However, both these transgenic plants have high drought tolerance as a result of superior water retention abilities, lower transpiration rates, and reduced stomatal apertures due to elevated ABA production. Interestingly, 35S:GaMYB85 plants have reduced stomatal density but enlarged stomatal size, which can result in enhanced photosynthetic ability of plants by some unknown mechanism. This warrants further studies to gain insights into the possible function of the ABA transduction pathway in GaMYB85-mediated roles in reduced stomatal apertures, which helps to maintain a balance between the rates of transpiration and photosynthetic capabilities of plant during drought stress responses.
Moreover, several overexpression studies have demonstrated the use of ABA-related marker genes involved in stress-related phenotypes in Arabidopsis [31, 56, 63]. Similarly, 35S:GaMYB85 overexpression led to the up regulation of RD22, RD29A, ADH1, AB15, and P5CS. The AB15 gene encodes a bZIP TF, and is an ABA-responsive gene known to play a prominent role during the seed germinating period during drought stress [64, 65]. Moreover, d-pyrroline-5-carboxylase synthetase (P5CS) plays a key role in the initiation step for proline synthesis during dehydration or osmotic stress, and it has been revealed that up-regulation of the P5CS gene in 35S:GaMYB85 plants corroborated well with the findings of studies on OsMYB48–1, AtLOS5, and TaNAC47 [52, 53, 59]. The RD29A gene codes for a hydrophilic protein and is known for the presence of DRE or related promoter motif regions. It is activated by the combined action of DRE and ABRE cis motif elements, which enables it to work both in ABA-dependent and ABA-independent manners . ABA-responsive expression of RD22 is mainly due to co-expression activation of AtMYB2/AtMYC2. This is in contrast to ADH1, which only requires activated AtMYB2 to act in a protective protein . The above findings for GaMYB85 imply that it functions in an ABA-dependent manner, and plays an important role in drought stress tolerance, which has important implications for breeding drought-tolerant cotton varieties.
To summarize, ectopic expression of GaMYB85 in Arabidopsis led to enhanced drought avoidance, elevated survival rates, higher accumulation of the compatible osmolyte proline, good germination rates under osmotic and salt stress, reduced water loss rates with improved RWC, increased ABA sensitivity at the germination and post-germination stages, a reduction in the number of ABA-induced stomatal apertures, and up-regulated transcription of ABA-mediated stress-responsive marker genes. In the light of the results of this study, we speculate that 35S: GaMYB85 could confer good drought, salt, and freezing tolerance in cotton crops. Our observations on the activity of the R2R3 MYB transcription factor GaMYB85 in transgenic Arabidopsis plants greatly enhances our perception about its possible function in response to environmental cues, and it can be considered as a novel candidate gene for future developments in cotton breeding.
Transgenic plant construction and screening
The presence of the CaMV-35S promoter driven pCAMBIA3300-GaMYB85 construct in A. tumefaciens strain GV3101 was confirmed using a GaMYB85 sense and antisense primer pair (Additional file 3), and was ectopically expressed in A. thaliana (Col-0) using the floral dip method with minor modifications . The infiltration media used for transformation comprised 2.215 g/L MS containing 50 g/L of sucrose, 0.5 g/L of MES, (330 μL/L) of Silwet-77 and 0.01 mg/L of 6-BA at pH 5.7. The infiltrated Arabidopsis was grown under the following conditions: 16 h light/8 h dark, 60% RH, and 22°C. Transgenic T0 seedlings were screened using 1 mg/L BASTA, which was sprayed twice on 7-d-old seedlings grown in soil pots (Additional file 4). The surviving seedlings were set to obtain T1 seeds, which were then confirmed for T-DNA integration in transgenic plants using a PCR Mighty Amp Genotyping Kit (Takara, China) as shown in (Fig. 2a), using the sense 35S primer and the antisense gene primer. Wild-type (WT) plants were used as a control. Ten T2 lines with the correct segregation ratio (3:1) were selected and confirmed by qRT-PCR (Fig. 2b). Three T3 homozygous lines were selected and used for functional validation investigations (Additional file 5).
Germination and root elongation assays
To evaluate germination in response to simulated osmotic, salt, and ABA stresses, seeds from 35S:GaMYB85 transgenic lines (L3, L4, and L7) and WT were sterilized, stratified, and sown in triplicate on half-strength MS supplemented with different mannitol concentrations (0,100, 200, and 300 mM), exogenous ABA (0, 0.3, 0.5, 1, 2, and 5 μM) and NaCl (0, 50, 100, 125, and 150 mM). The plants were scored based on non-green phenotype or dead cotyledons on the 10th day post-germination . Furthermore, for seedling root length elongation assay on mannitol-, NaCl-, and ABA-supplemented MS, the methods described by  were followed. Three independent experiments were conducted and significant differences were determined using Student’s t-test.
Drought and freezing tolerance assay
T3 homozygous transgenic line (L3, L4, and L7) and WT seeds were sterilized with 10% bleach for 10 min, rinsed with water, and stratified at 4 °C for 3 days before the seeds were transferred to MS. One-week-old seedlings were transferred from MS to pots containing a well-watered vermiculite and humus mix, and grown for 2 weeks. Thereafter, water was withheld for 2 weeks to simulate drought stress treatment. Subsequently, pots were re-watered and plant revival rates were scored after 3 d. Plants showing green healthy leaves after water replenishment were scored as surviving. The ratios of surviving to dead plants were calculated and the experiment was repeated three times . For the freezing tolerance experiment, 3-week-old overexpressing transgenic lines and control WT plants were subjected to a temperature of −10°C for 3 h. Subsequently, survival rates were calculated as previously described by . All experiments were repeated three times using seeds of WT plants and the three transgenic lines independently.
Measurements of transpirational WLR and RWC
The water loss rate was determined as described by . Detached leaves from 4-week-old test and control plants were immediately weighed to determine fresh weights (FW). Thereafter, at various time intervals, weights were recorded while samples were retained on a bench at 22 °C RT with a humidity level of 45% ± 5%. Fresh weights were calculated relative to plant initial weights. The relative water content of leaves was calculated using the method described by . RWC percentage = (FW − DW)/(TW − DW) × 100. After determining fresh weights, the leaves were submerged in water for 4 h and turgid weights (TW) were recorded. Dry weights (DW) of leaves were recorded by drying samples at 80 °C for approximately 72 h.
Proline and chlorophyll contents
Endogenous proline content in drought-stressed transgenic and WT plants was measured using a colorimetric PRO Kit (Jiancheng Bioengineering Institute, Nanjing, China). Three biological repeats were used, and proline absorbances at a wavelength of 520 nm were measured for determination of proline concentration.
Chlorophyll content was calculated using the formula described by  as follows: ((O.D 665 nm × 13.95 - O.D 649 nm × 6.88) + (O.D 649 nm × 24.96 - O.D 665 nm × 7.32))/(sample weight). The sample extraction was performed using 0.1 g of rosette leaves in 1.5 mL 95% ethanol at RT in a dark room. The absorbances of extracted chlorophyll were measured at 649 nm and 665 nm. Test and control samples were measured three times and the results were averaged. The means were compared using Duncan’s multiple range test.
Stomatal measurements and determination of opening rate in response to abscisic acid treatment
To investigate if stomatal pore closure is sensitive to ABA, we examined the effect of ectopic expression of GaMYB85 on stomatal opening rate of leaves under a microscope. The stomatal pores were initially opened by placing detached leaves from 3-week-old plants in a stomata opening solution (10 mM CaCl2, 50 mM KCl, and 5 mM MES, pH 6.15)  for 2 h in an illuminated growth chamber at 95% RH. Stomatal apertures were determined after 2.5 h. Two concentrations of ABA (5 and 10 μM) were applied, whereas control experiments were performed without using ABA. Samples of young leaf epidermis of transgenic and WT plants were peeled and observed under an OLYMPUS Bx51 microscope for stomata density evaluation and measurement of guard cell width to length ratio. IMAGEJ 1.51d software  was used to measure the size of guard cells.
Expression analysis of marker genes by qRT-PCR
For transcript analysis of stress-responsive marker genes, 2-week-old transgenic and WT seedlings treated with 100 μM ABA were used. RNA extraction was performed using an RNA-prep Pure Plant kit (Tiangen, China), followed by first-strand cDNA synthesis using PrimeScript RT Master Mix (Takara, Clontech, China). Quantitative RT-PCR was carried out using a 7900HT detection system (Applied Biosystems), using SYBR Premix ExTaq™ (Takara, Clontech, China) according to manufacturer’s protocol. AtUBQ10 (Accession no: AT4G05320) was used as a control gene. Three biological replicates were run using independent cDNA preparations and three technical replicates, and relative transcripts were computed using the 2-∆∆Ct method based on CT values .
Sequence and phylogenetic analysis
GaMYB85 was retrieved from the cotton genome project database (http: //cgp.genomics.org.cn/page/species/blast.jsp.) and designated GaMYB85 (cotton_A_21601). Motif analysis was performed using SMART (http://smart.embl-heidelberg.de/), whereas intron–exon analysis was carried out using the GENE Structure Display Server available online (http://gsds.cbi.pku.edu.cn). GaMYB85 protein physio-chemical properties, such as MW and pI, were evaluated using the ExPASy proteomic portal (http://www.expasy.org/proteomics). Monocot and dicot R2R3 MYB homologs were retrieved using the Blastp tool (https://www.ncbi.nlm.nih.gov/) and known R2R3 MYB were used in the construction of a cladogram based on the neighbor-joining method using MEGA 6.0. The multiple sequence alignment of GaMYB85 R2R3 homologs was performed using the EMBL-EBI Muscle online tool (http://www.ebi.ac.uk/Tools/msa/muscle/).
Statistical analysis of data
Statistical analysis was performed on data derived from three independent replicate experiments, using analysis of variance and Student’s t-test. Duncan’s multiple range test was applied to determine variation among treatment means of test and control lines.
DNA binding domain;
- GaMYB85 :
Gene in Gossipium arboreum;
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We thank Prof. Jia Li (School of Life Sciences, Lanzhou University, Lanzhou) for providing us A. tumefaciens strain GV3101 and seeds of A. thaliana respectively. This work was supported by the Major Program of Joint Funds (Sinkiang) of the National Natural Science Foundation of China (grant U1303282).
This work was supported by the Major Program of Joint Funds (Sinkiang) of the National Natural Science Foundation of China (grant U1303282).
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Additional file 1:
Bioinformatics sequence analysis of GaMYB85 protein. (DOC 660 kb)
Additional file 2:
Alignment of GaMYB85 with the deduced homologous amino acid sequences of R2R3 MYB retrieved from Blastp NCBI and known R2R3 MYB. (DOCX 469 kb)
Additional file 3:
The primers sequences used for GaMYB85 study. (DOCX 13 kb)
Additional file 4:
35S:GaMYB85 over-expressed positive transgenic plants screening in BASTA screening at T0 and T3 stages. (DOCX 1186 kb)
Additional file 5:
Survival percentage of 35S:GaMYB85 transgenic plants in 6% BASTA selection medium. (DOCX 11 kb)
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Butt, H.I., Yang, Z., Gong, Q. et al. GaMYB85, an R2R3 MYB gene, in transgenic Arabidopsis plays an important role in drought tolerance. BMC Plant Biol 17, 142 (2017). https://doi.org/10.1186/s12870-017-1078-3
- MYB transcription factor
- Abiotic stress tolerance
- Abscisic acid