Overexpression of a Fragaria vesca MYB Transcription Factor Gene (FvMYB82) Increases Salt and Cold Tolerance in Arabidopsis thaliana

The MYB transcription factor (TF) family is one of the largest transcription families in plants, which is widely involved in the responses to different abiotic stresses, such as salt, cold, and drought. In the present study, a new MYB TF gene was cloned from Fragaria vesca (a diploid strawberry) and named FvMYB82. The open reading frame (ORF) of FvMYB82 was found to be 960 bp, encoding 319 amino acids. Sequence alignment results and predictions of the protein structure indicated that the FvMYB82 contained the conserved R2R3-MYB domain. Subcellular localization analysis showed that FvMYB82 was localized onto the nucleus. Furthermore, the qPCR showed that the expression level of FvMYB82 was higher in new leaves and roots than in mature leaves and stems. When dealing with different stresses, the expression level of FvMYB82 in F. vesca seedlings changed markedly, especially for salt and cold stress. When FvMYB82 was introduced into Arabidopsis thaliana, the tolerances to salt and cold stress of FvMYB82-OE A. thaliana were greatly improved. When dealt with salt and cold treatments, compared with wild-type and unloaded line (UL) A. thaliana, the transgenic lines had higher contents of proline and chlorophyll, as well as higher activities of superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT). However, the transgenic A. thaliana had lower level of malondialdehyde (MDA) and electrolytic leakage (EL) than wild-type and UL A. thaliana under salt and cold stress. Meanwhile, FvMYB82 can also regulate the expression of downstream genes associated with salt stress (AtSnRK2.4, AtSnRK2.6, AtKUP6, and AtNCED3) and cold stress (AtCBF1, AtCBF2, AtCOR15a, and AtCOR78). Therefore, these results indicated that FvMYB82 probably plays an important role in the response to salt and cold stresses in A. thaliana by regulating downstream related genes.


Introduction
Many factors in the growth environment of plants are changeable and may cause biotic or abiotic stress, which will hinder the growth of plants and can even cause irreversible damage [1]. In recent years, with technological advances in molecular biology, it is increasingly feasible to improve the adaptability of plants to the external environment through genetic manipulation. Transcription factors and their regulatory functions have an important place in current plant research. Transcription factors in plants are activated by specific signal transduction pathways in response to a specific stress stimulus. Transcription

Cloning and Bioinformatic Analysis of FvMYB82
The full-length FvMYB82 gene cloned from Fragaria vesca was 960 bp and encoded 319 amino acids ( Figure S1). The ExPASy ProtParam tool (SIB Swiss Institute of Bioinformatics, Swiss. https://web.expasy.org/protparam/, accessed on 1 June 2022) predicted that the encoded protein had a theoretical molecular weight of 36.116 kDa and a theoretical isoelectric point of 6.64. The Ser (10.7%), Thr (9.1%), Asn (7.5%), and Lys (7.2%) residues predominated in the amino acid composition of the FvMYB82 protein. The total number of negatively charged residues (Asp + Glu) was 41, whereas the total number of positively charged residues (Arg + Lys) was 39. The overall average hydropathicity of FvMYB82 was −0.971, indicating that the protein was hydrophilic.
The FvMYB82 gene included two MYB conserved DNA-binding domains, consistent with 13 species (Figure 1A). A phylogenetic tree revealed that FvMYB82 was clustered in the same lineage with RcMYB82 of Rosa chinensis, and thus the two genes showed the highest homology ( Figure 1B). Analysis of the secondary structure revealed that the FvMYB82 protein comprised 24.45% alpha helices, 6.90% beta turns, 12.54% extended strands, and 56.11% random coils (Figure 2A). The FvMYB82 amino acid sequence contained two SANTconserved domains ( Figure 2B), one located at 16-69 aa and the other located at 72-120 aa. The presence of these domains showed that FvMYB82 was a member of the R2R3-MYB family. Analysis with the SWISS-MODEL online tool predicted a tertiary structure with a HTH region, consistent with the predicted secondary structure for FvMYB82 ( Figure 2C). dues (Asp + Glu) was 41, whereas the total number of positively c Lys) was 39. The overall average hydropathicity of FvMYB82 wa the protein was hydrophilic.
The FvMYB82 gene included two MYB conserved DNA-bind with 13 species ( Figure 1A). A phylogenetic tree revealed that FvM the same lineage with RcMYB82 of Rosa chinensis, and thus the highest homology ( Figure 1B). Analysis of the secondary stru FvMYB82 protein comprised 24.45% alpha helices, 6.90% beta strands, and 56.11% random coils (Figure 2A). The FvMYB82 am tained two SANT-conserved domains ( Figure 2B), one located at located at 72-120 aa. The presence of these domains showed that F of the R2R3-MYB family. Analysis with the SWISS-MODEL online structure with a HTH region, consistent with the predicted s FvMYB82 ( Figure 2C).

FvMYB82 Was Localized onto the Nucleus
The FvMYB82 gene was connected to the pCAMBIA2300 vector. The resulting 35S::FvMYB82-GFP construct was bombarded onto onion epidermal cells, so as to visualize the subcellular localization of the FvMYB82 protein. As observed with a confocal laser scanning microscope, the fluorescence of the control 35S::GFP construct was distributed throughout the cell in the nucleus, cell membrane, and cytoplasm, whereas the fluorescence signal of the 35S::FvMYB82-GFP fusion protein was localized onto the nucleus. This was consistent with the effect after DAPI staining ( Figure 3).

Expression Level Analysis of FvMYB82 in F. vesca Seedlings
The expression patterns of FvMYB82 in immature leaves, mature leaves, stems, and roots of F. vesca were analyzed with quantitative RT-PCR technology. The expression level of FvMYB82 was highest in immature leaves, but it was much lower in stems and mature leaves ( Figure 4A). In immature leaves, low temperature was the first abiotic stress treatment to induce FvMYB82 expression. The expression level was significantly higher under cold stress than that of the control (CK) and under salt, drought, heat, or ABA treatment. The expression of cold stress reached the peak at 2 h and decreased gradually within 12

FvMYB82 Was Localized onto the Nucleus
The FvMYB82 gene was connected to the pCAMBIA2300 vector. The resulting 35S::FvMYB82-GFP construct was bombarded onto onion epidermal cells, so as to visualize the subcellular localization of the FvMYB82 protein. As observed with a confocal laser scanning microscope, the fluorescence of the control 35S::GFP construct was distributed throughout the cell in the nucleus, cell membrane, and cytoplasm, whereas the fluorescence signal of the 35S::FvMYB82-GFP fusion protein was localized onto the nucleus. This was consistent with the effect after DAPI staining ( Figure 3).

FvMYB82 Was Localized onto the Nucleus
The FvMYB82 gene was connected to the pCAMBIA2300 vector. The resulting 35S::FvMYB82-GFP construct was bombarded onto onion epidermal cells, so as to visualize the subcellular localization of the FvMYB82 protein. As observed with a confocal laser scanning microscope, the fluorescence of the control 35S::GFP construct was distributed throughout the cell in the nucleus, cell membrane, and cytoplasm, whereas the fluorescence signal of the 35S::FvMYB82-GFP fusion protein was localized onto the nucleus. This was consistent with the effect after DAPI staining ( Figure 3).

Expression Level Analysis of FvMYB82 in F. vesca Seedlings
The expression patterns of FvMYB82 in immature leaves, mature leaves, stems, and roots of F. vesca were analyzed with quantitative RT-PCR technology. The expression level of FvMYB82 was highest in immature leaves, but it was much lower in stems and mature leaves ( Figure 4A). In immature leaves, low temperature was the first abiotic stress treatment to induce FvMYB82 expression. The expression level was significantly higher under cold stress than that of the control (CK) and under salt, drought, heat, or ABA treatment. The expression of cold stress reached the peak at 2 h and decreased gradually within 12

Expression Level Analysis of FvMYB82 in F. vesca Seedlings
The expression patterns of FvMYB82 in immature leaves, mature leaves, stems, and roots of F. vesca were analyzed with quantitative RT-PCR technology. The expression level of FvMYB82 was highest in immature leaves, but it was much lower in stems and mature leaves ( Figure 4A). In immature leaves, low temperature was the first abiotic stress treatment to induce FvMYB82 expression. The expression level was significantly higher under cold stress than that of the control (CK) and under salt, drought, heat, or ABA treatment. The expression of cold stress reached the peak at 2 h and decreased gradually within 12 h. In the other stress treatments, the expression level in immature leaves in the salt and drought treatments peaked at 8 h. That of the heat treatment peaked at 2 h, and it was highest at 6 h under ABA treatment ( Figure 4B). In the roots, cold treatment induced FvMYB82 expression first, and the expression level was significantly higher than that in the salt, drought, heat, and ABA treatments and the CK. The highest expression level in the roots was detected at 4 h and thereafter decreased within 12 h. The expression level in the roots under salt or ABA treatment peaked at 2 h, that in the drought treatment peaked at 4 h, and that in the hot treatment expression peaked at 6 h ( Figure 4C). qPCR analysis of strawberry showed that the expression of FvMYB82 was relatively significant under salt stress, low-temperature stress, ABA stress and drought stress. We preliminarily conducted salt stress and low-temperature stress.
Int. J. Mol. Sci. 2022, 23, 10538 h. In the other stress treatments, the expression level in immature leaves in the s drought treatments peaked at 8 h. That of the heat treatment peaked at 2 h, and highest at 6 h under ABA treatment ( Figure 4B). In the roots, cold treatment in FvMYB82 expression first, and the expression level was significantly higher than the salt, drought, heat, and ABA treatments and the CK. The highest expression the roots was detected at 4 h and thereafter decreased within 12 h. The expression the roots under salt or ABA treatment peaked at 2 h, that in the drought treatment at 4 h, and that in the hot treatment expression peaked at 6 h ( Figure 4C). qPCR a of strawberry showed that the expression of FvMYB82 was relatively significant salt stress, low-temperature stress, ABA stress and drought stress. We preliminari ducted salt stress and low-temperature stress.

Overexpression of FvMYB82 in A. thaliana Enhanced Salt Tolerance
Among 12 the transgenic A. thaliana plants, only five lines (L1, L2, L3, L4, a were identified as transgenic plants by using the real-time fluorescent quantitativ (qPCR), with the wild-type (WT) and unloaded line (UL) lines as controls (Figu Therefore, T3 transgenic A. thaliana lines were used as test materials for further an According to the statistics of the germination rates of WT, UL, and transgenic lines found that the germination rates of the five groups of A. thaliana plants were not d under normal growth conditions. Under salt stress, the germination rates of WT a were 25% and 28%, respectively. The germination rates of L1, L3 and L5 lines we 68%, and 69%, respectively ( Figure S2A).

Overexpression of FvMYB82 in A. thaliana Enhanced Salt Tolerance
Among 12 the transgenic A. thaliana plants, only five lines (L1, L2, L3, L4, and L5) were identified as transgenic plants by using the real-time fluorescent quantitative PCR (qPCR), with the wild-type (WT) and unloaded line (UL) lines as controls ( Figure 5A). Therefore, T 3 transgenic A. thaliana lines were used as test materials for further analysis. According to the statistics of the germination rates of WT, UL, and transgenic lines, it was found that the germination rates of the five groups of A. thaliana plants were not different under normal growth conditions. Under salt stress, the germination rates of WT and UL were 25% and 28%, respectively. The germination rates of L1, L3 and L5 lines were 70%, 68%, and 69%, respectively ( Figure S2A). The response of FvMYB82 to salt stress was further explored by treating T3 transgenic FvMYB82-OE A. thaliana (L1, L3, and L5), WT, and UL with 200 mM NaCl for 7 days, followed by irrigation with water for 3 days for recovery. Under the non-stress condition (0 d), the transgenic lines (L1, L3, and L5), WT, and UL exhibited an identical phenotype. After 200 mM NaCl treatment for 7 days, the leaves of all lines were yellow, and after recovery (water treatment) for 3 days, the phenotypic recovery of the WT and UL was inferior to that of the transgenic plants ( Figure 5B). The percentage survival of the L1, L3, and L5 lines was 78%, 73%, and 75%, respectively, whereas the WT and UL had survival rates of 21% and 32%, respectively. The FvMYB82-OE A. thaliana showed significantly increased survival under salt stress ( Figure 5C).
All A. thaliana lines grown in the control environment and under salt stress were analyzed for physiological indicators. Overexpression of FvMYB82 in transgenic A. thaliana reduced the increase in malondialdehyde (MDA) content in response to salt treatment, whereas the proline content was increased significantly and activities of catalase (CAT), peroxidase (POD), and superoxide dismutase (SOD) were higher in the transgenic overexpression lines than the WT under salt stress ( Figure 6). The chlorophyll content was decreased in all lines under salt stress and was lower in the WT and UL compared with the L1, L3, and L5 lines. The EL of WT and UL was significantly higher than that of transgenic type under salt stress ( Figure S3A). These results indicated that the high expression of FvMYB82 in A. thaliana could enhance plants' resistance to high salt stress. The response of FvMYB82 to salt stress was further explored by treating T 3 transgenic FvMYB82-OE A. thaliana (L1, L3, and L5), WT, and UL with 200 mM NaCl for 7 days, followed by irrigation with water for 3 days for recovery. Under the non-stress condition (0 d), the transgenic lines (L1, L3, and L5), WT, and UL exhibited an identical phenotype. After 200 mM NaCl treatment for 7 days, the leaves of all lines were yellow, and after recovery (water treatment) for 3 days, the phenotypic recovery of the WT and UL was inferior to that of the transgenic plants ( Figure 5B). The percentage survival of the L1, L3, and L5 lines was 78%, 73%, and 75%, respectively, whereas the WT and UL had survival rates of 21% and 32%, respectively. The FvMYB82-OE A. thaliana showed significantly increased survival under salt stress ( Figure 5C).
All A. thaliana lines grown in the control environment and under salt stress were analyzed for physiological indicators. Overexpression of FvMYB82 in transgenic A. thaliana reduced the increase in malondialdehyde (MDA) content in response to salt treatment, whereas the proline content was increased significantly and activities of catalase (CAT), peroxidase (POD), and superoxide dismutase (SOD) were higher in the transgenic overexpression lines than the WT under salt stress ( Figure 6). The chlorophyll content was decreased in all lines under salt stress and was lower in the WT and UL compared with the L1, L3, and L5 lines. The EL of WT and UL was significantly higher than that of transgenic type under salt stress ( Figure S3A). These results indicated that the high expression of FvMYB82 in A. thaliana could enhance plants' resistance to high salt stress.

Overexpression of FvMYB82 Improved the Expression Levels of Salt Tolerance-Related Genes
Salt tolerance is dependent on the ABA signaling pathway. Therefore, expression analysis of AtSnRK2.4 and AtSnRK2.6, two genes involved in ABA signal transduction [22,23], in A. thaliana overexpressing FvMYB82 was performed ( Figure 7). The expression levels of AtSnRK2.4 and AtSnRK2.6 in each A. thaliana line did not differ in the non-stress environment. However, under salt stress, the expression levels of AtSnRK2.4 and AtSnRK2.6 in WT plants were much lower than those in FvMYB82-overexpressing plants, indicating that FvMYB82 may function as an upstream transcription factor that positively regulated the downstream genes AtSnRK2.4 and AtSnRK2.6 under salt stress. These results also indicated that ABA signal transduction was responsive to salt stress. Kup6 potassium transporter plays a role in ABA biosynthesis during osmoregulation under the control of ABA [24]. ABA biosynthesis in A. thaliana requires an ABA distal element of the AtNCED3 promoter [25]. In the meantime, the expression levels of AtKUP6 and AtNCED3 were significantly higher under salt stress than under the non-stress condition, and the expression levels were significantly higher in the transgenic A. thaliana lines than the WT. These findings suggested that FvMYB82 modulated crucial genes involved in plant salt stress and enhanced plant salt tolerance.

Overexpression of FvMYB82 Improved the Expression Levels of Salt Tolerance-Related Genes
Salt tolerance is dependent on the ABA signaling pathway. Therefore, expression analysis of AtSnRK2.4 and AtSnRK2.6, two genes involved in ABA signal transduction [22,23], in A. thaliana overexpressing FvMYB82 was performed (Figure 7). The expression levels of AtSnRK2.4 and AtSnRK2.6 in each A. thaliana line did not differ in the non-stress environment. However, under salt stress, the expression levels of AtSnRK2.4 and AtSnRK2.6 in WT plants were much lower than those in FvMYB82-overexpressing plants, indicating that FvMYB82 may function as an upstream transcription factor that positively regulated the downstream genes AtSnRK2.4 and AtSnRK2.6 under salt stress. These results also indicated that ABA signal transduction was responsive to salt stress. Kup6 potassium transporter plays a role in ABA biosynthesis during osmoregulation under the control of ABA [24]. ABA biosynthesis in A. thaliana requires an ABA distal element of the At-NCED3 promoter [25]. In the meantime, the expression levels of AtKUP6 and AtNCED3 were significantly higher under salt stress than under the non-stress condition, and the expression levels were significantly higher in the transgenic A. thaliana lines than the WT. These findings suggested that FvMYB82 modulated crucial genes involved in plant salt stress and enhanced plant salt tolerance.

Overexpression of FvMYB82 Improved the Expression Levels of Salt Tolerance-Related Genes
Salt tolerance is dependent on the ABA signaling pathway. Therefore, expression analysis of AtSnRK2.4 and AtSnRK2.6, two genes involved in ABA signal transduction [22,23], in A. thaliana overexpressing FvMYB82 was performed (Figure 7). The expression levels of AtSnRK2. 4 and AtSnRK2.6 in each A. thaliana line did not differ in the non-stress environment. However, under salt stress, the expression levels of AtSnRK2. 4 and AtSnRK2.6 in WT plants were much lower than those in FvMYB82-overexpressing plants, indicating that FvMYB82 may function as an upstream transcription factor that positively regulated the downstream genes AtSnRK2.4 and AtSnRK2.6 under salt stress. These results also indicated that ABA signal transduction was responsive to salt stress. Kup6 potassium transporter plays a role in ABA biosynthesis during osmoregulation under the control of ABA [24]. ABA biosynthesis in A. thaliana requires an ABA distal element of the AtNCED3 promoter [25]. In the meantime, the expression levels of AtKUP6 and AtNCED3 were significantly higher under salt stress than under the non-stress condition, and the expression levels were significantly higher in the transgenic A. thaliana lines than the WT. These findings suggested that FvMYB82 modulated crucial genes involved in plant salt stress and enhanced plant salt tolerance.

Overexpression of FvMYB82 Improved the Cold Tolerance of A. thaliana
The 4-week-old seedlings of the WT, UL, and T 3 FvMYB82-OE A. thaliana (L1, L3 and L5) were cultured at 4 • C for 48 h in an incubator under a 14 h/10 h (light/dark) photoperiod, then subjected to −6 • C freezing treatment for 14 h, and then returned to the normal environment (14 h, 22 • C/10 h 18 • C (light/dark)) for 7 days. The phenotype of the FvMYB82-overexpressing A. thaliana plants was almost identical to that of the WT and UL in the control environment. However, cold treatment caused an obvious difference in phenotype among these lines ( Figure 8A). Compared with transgenic L1, L3 and L5, the leaves of WT and UL plants were more damaged and difficult to recover. The percentage survival of the three FvMYB82-overexpression lines was 78%, 79%, and 77%, whereas that of the WT was 25% and the UL was 30% ( Figure 8B). Meanwhile, with cold treatment, the germination rates of WT and UL were 30% and 26%, respectively. The germination rates of L1, L3, and L5 lines were 73%, 74%, and 68%, respectively ( Figure S2B).
average of three replicates. Significant differences are marked with an asterisk above the e (** p ≤ 0.01).

Overexpression of FvMYB82 Improved the Cold Tolerance of A. thaliana
The 4-week-old seedlings of the WT, UL, and T3 FvMYB82-OE A. thaliana (L1, L5) were cultured at 4 °C for 48 h in an incubator under a 14 h/10 h (light/dark) ph iod, then subjected to −6 °C freezing treatment for 14 h, and then returned to the environment (14 h, 22 °C/10 h 18 °C (light/dark)) for 7 days. The phenotype FvMYB82-overexpressing A. thaliana plants was almost identical to that of the WT in the control environment. However, cold treatment caused an obvious difference notype among these lines ( Figure 8A). Compared with transgenic L1, L3 and L5, the of WT and UL plants were more damaged and difficult to recover. The percenta vival of the three FvMYB82-overexpression lines was 78%, 79%, and 77%, whereas the WT was 25% and the UL was 30% ( Figure 8B). Meanwhile, with cold treatm germination rates of WT and UL were 30% and 26%, respectively. The germinatio of L1, L3, and L5 lines were 73%, 74%, and 68%, respectively ( Figure S2B). Physiological indicators associated with cold stress in transgenic A. thaliana li L3, and L5) were analyzed. Almost no differences in MDA, chlorophyll, and proli tents, and POD, SOD, and CAT activities among these lines and the WT under the condition (22 °C) (Figure 9). The activities of POD, SOD, and CAT and the proline increased after cold treatment, and the proline content increased to a greater ex transgenic A. thaliana compared with the WT. The content of MDA increased und treatment, but the degree of increase was alleviated in the transgenic lines compar the WT. The chlorophyll content of A. thaliana overexpressing FvMYB82 and the creased under cold treatment, but the decline was strongly alleviated in the tra lines. The EL of WT and UL was significantly higher than that of transgenic type cold stress ( Figure S3B). In conclusion, a high level of FvMYB82 expression in A. may increase its resistance to low temperatures. Physiological indicators associated with cold stress in transgenic A. thaliana lines (L1, L3, and L5) were analyzed. Almost no differences in MDA, chlorophyll, and proline contents, and POD, SOD, and CAT activities among these lines and the WT under the control condition (22 • C) (Figure 9). The activities of POD, SOD, and CAT and the proline content increased after cold treatment, and the proline content increased to a greater extent in transgenic A. thaliana compared with the WT. The content of MDA increased under cold treatment, but the degree of increase was alleviated in the transgenic lines compared with the WT. The chlorophyll content of A. thaliana overexpressing FvMYB82 and the WT decreased under cold treatment, but the decline was strongly alleviated in the transgenic lines. The EL of WT and UL was significantly higher than that of transgenic type under cold stress ( Figure S3B). In conclusion, a high level of FvMYB82 expression in A. thaliana may increase its resistance to low temperatures.

Overexpression of FvMYB82 Enhanced the Expression Levels of Cold Tolerance-Related Genes
The CBF (CRT-Binding Factor/DRE-Binding Protein) transcription factor family is commonly used as an indicator of cold response pathways in A. thaliana [26]. Therefore, the expression of several cold-responsive transcription factors downstream of MYB genes (AtCBF1, AtCBF2, AtCOR15a, and AtCOR78) under cold treatment was analyzed in FvMYB82-overexpression A. thaliana lines and the WT (Figure 10). The plants were treated at −6 °C for 14 h. The expression levels of AtCBF1, AtCBF2, AtCOR15a, and AtCOR78 in the WT and UL were significantly lower than those in the FvMYB82-overexpression lines, indicating that FvMYB82, as an upstream transcription factor, positively regulated the downstream genes AtCBF1 and AtCBF2. Subsequently, the expression levels of AtCOR15a and AtCOR78 were increased, and ultimately the cold tolerance of the plants was greatly improved.

Overexpression of FvMYB82 Enhanced the Expression Levels of Cold Tolerance-Related Genes
The CBF (CRT-Binding Factor/DRE-Binding Protein) transcription factor family is commonly used as an indicator of cold response pathways in A. thaliana [26]. Therefore, the expression of several cold-responsive transcription factors downstream of MYB genes (AtCBF1, AtCBF2, AtCOR15a, and AtCOR78) under cold treatment was analyzed in FvMYB82-overexpression A. thaliana lines and the WT (Figure 10). The plants were treated at −6 • C for 14 h. The expression levels of AtCBF1, AtCBF2, AtCOR15a, and AtCOR78 in the WT and UL were significantly lower than those in the FvMYB82-overexpression lines, indicating that FvMYB82, as an upstream transcription factor, positively regulated the downstream genes AtCBF1 and AtCBF2. Subsequently, the expression levels of At-COR15a and AtCOR78 were increased, and ultimately the cold tolerance of the plants was greatly improved.

Overexpression of FvMYB82 Enhanced the Expression Levels of Cold Tolerance-Related Genes
The CBF (CRT-Binding Factor/DRE-Binding Protein) transcription factor family is commonly used as an indicator of cold response pathways in A. thaliana [26]. Therefore, the expression of several cold-responsive transcription factors downstream of MYB genes (AtCBF1, AtCBF2, AtCOR15a, and AtCOR78) under cold treatment was analyzed in FvMYB82-overexpression A. thaliana lines and the WT (Figure 10). The plants were treated at −6 °C for 14 h. The expression levels of AtCBF1, AtCBF2, AtCOR15a, and AtCOR78 in the WT and UL were significantly lower than those in the FvMYB82-overexpression lines, indicating that FvMYB82, as an upstream transcription factor, positively regulated the downstream genes AtCBF1 and AtCBF2. Subsequently, the expression levels of AtCOR15a and AtCOR78 were increased, and ultimately the cold tolerance of the plants was greatly improved.

Discussion
The composition of MYB transcription factors in plants contains a conserved domain, which is composed of one to four incomplete repeated amino acid sequences (R1, R2, and R3), which is called the R structure. The largest family of MYB proteins in plants is the R2R3-MYB family, which has two conserved domains [27]. In the present study, wild-type forest strawberry was used as the experimental material and the sequence of FvMYB82 was identified from the strawberry gene bank (http://bioinformatics.towson. edu/strawberry/newpage/TF_Clustering.aspx (accessed on 22 September 2020)). Primers were designed using DNAMAN and the gene sequence was cloned. The length of the FvMYB82 nucleotide sequence was 960 bp, encoding 320 amino acids, and the predicted protein had an average hydrophilicity of 1.02, and thus was predicted to be a relatively hydrophilic protein. FvMYB82 contained two SANT-MYB DNA-binding domains, which are conserved domains typical of R2R3-MYB family members; thus, it was speculated to be a typical R2R3-MYB gene. Multiple sequence alignment between FvMYB82 protein sequence and MYB protein sequence of other species showed that FvMYB82 protein and other MYB family proteins had high similarity in the conserved sequence, but there was a big difference in the non-conserved region, which was consistent with the characteristics of transcription factors. The two SANT-conserved domains showed similarity to MbMYB4 from Malus baccata [28]. A phylogenetic tree revealed that FvMYB82 was phylogenetically closest to RcMYB82.
Previous studies have reported that transcription factors mainly function in the nucleus of cells. For example, the MbMYB4 protein is localized to the nucleus [28]. Using the particle bombardment method, the FvMYB82-GFP fusion vector was inserted into onion epidermal cells for transient expression and observed with a confocal microscope. As a control, the green fluorescent protein (GFP) was distributed throughout the whole cell, while the fluorescence of the FvMYB82-GFP fusion protein was only localized onto the nucleus ( Figure 3E). DAPI staining of the cell nucleus can further identify that FvMYB82 protein was located onto the cell nucleus. These results were consistent with those for M. baccata [28]. However, the subcellular localization of certain MYB proteins may differ in other plant species. The tomato SlMYBl protein was localized in the mitochondria [29], and in Prunus campanulata, PcMYB was localized on the plasma membrane [30].
The MYB transcription factors play important roles in plant growth processes. Some MYB genes regulate growth and development, and response to pathogen attack; some are involved in tolerance to cold, salt, drought, and other stresses; and some participate in plant morphogenesis. In A. thaliana, AtMYB58, AtMYB63, and AtMYB85 activate lignin synthesis in fibers and vascular bundles, thus improving the ability to resist stress [31]. A. thaliana AtMYB26 controls secondary wall deposition in the anther [32]. Trichomes are important epidermal structures in plants. Trichomes can reduce external environmental stress during plant growth and development and play a crucial role in plant stress responses [33]. The AtMYB82 transcription factor positively regulates trichome formation in A. thaliana, and the increase in trichome density correspondingly increases tolerance of salt and cold stress [34].
The expression pattern of FvMYB82 was indicated to be tissue specific in F. vesca. The expression level of FvMYB82 was highest in immature leaves and lowest in mature leaves of F. vesca, and the expression level in immature leaves was nine times that of mature leaves. The results showed, in accordance with MbMYB4 and MbMYB108 from M.baccata, that the MYB gene expression level in immature leaves were higher than in other tissues, indicating the new leaves may be more sensitive to external stress. For these reasons, young leaf and root were chosen for further identification. The present results showed that low temperature, salinity, drought, high temperature, and ABA induced high-expression levels of FvMYB82 in F. vesca, and that the expression levels varied with treatment duration. In a cold environment, the expression level of FvMYB82 was distinctly elevated. It peaked at 2 h in young leaf and peaked at 4h in root. Under salt stress, FvMYB82 expression peaked at 8 h in young leaf and peaked at 2 h in root, and in the young leaf, the maximum level was 4.6 times that of the control. The expression level of FvMYB82 under drought stress peaked at 8 h in young leaf and peaked at 4 h in root. The maximum was 9.2 times that of the control in young leaf and 9.1 times in root. These results indicated that FvMYB82 in different parts of the plant was responsive to cold, salt, and ABA treatment, which provided the basis for the subsequent analyses.
When plants are under stress, their cell plasma membranes become more permeable, electrolytes and soluble substances leak out, then EL increases. Therefore, the measurement of relative EL is a method used to determine the resistance of plants to stress [28]. In this study, under salt stress and cold stress, the germination rates of A. thaliana overexpressing FvMYB82 (L1, L3 and L5) were significantly higher than WT and UL, and the relative EL of (L1, L3 and L5) was significantly higher than that of the wild type. Thus, overexpression of FvMYB82 increased the tolerance of A. thaliana to salt and cold stresses. The contents of proline, chlorophyll, and MDA and activities of antioxidant enzymes are indicators of stress-induced damage to plants [35][36][37]. Proline can change the osmotic concentration of cells, which acts as an important osmotic regulator of plant cells. In this study, the contents of proline increased, becoming significantly higher than WT and UL, which showed that the salt-stress-induced transgenic lines improved the salt tolerance obviously. The increase in MDA content is an indicator of increased oxidative damage to membranes in plant cells [38], when WT, UL, and three lines (L1, L3, and L5) were under salt stress, MDA content of WT and UL was significantly higher than transgenic lines, indicating that WT and UL membranes were damaged more seriously. Under high salt stress, damage to the leaf cells results in reduction in the chlorophyll content, and the leaf color changes to yellow. Therefore, analysis of the chlorophyll content in the leaves can reveal the stress resilience of plants [39]. In this study, under salt stress, the leaves of WT and UL showed more yellow than FvMYB82-OE A. thaliana. Antioxidant enzymes eliminate excess oxidation products and protect cells from oxidative damage [40]. For these, the activities of antioxidant enzymes in plants indicates the degree of plant tolerance to stress. Under salt stress, the contents of CAT, SOD, and POD in transgenic lines (L1, L3, and L5) increased, becoming higher than WT and UL, indicating that FvMYB82-OE improved salt tolerance.
The ABA signaling pathway is responsive to salt stress. Previous studies have shown that the ABA content increases in plants under salt stress, and improved tolerance to salt stress is associated with an increase in ABA content. The ABA response elements (ABRE) and ABRE-binding proteins/ABRE-binding factors (AREB/ABFs) are critical in ABAdependent gene expression during stress response [41]. A. thaliana AtSnRK2.6 and other genes respond to ABA-dependent and ABA-independent pathways, whereas AtSnRK2.10 responds only to ABA-independent pathways [42]. The SnRK2 family plays a crucial role in the ABA signal transduction pathway. SnRK2 kinase activity is inhibited in the absence of ABA. Under salt stress, ABA receptor proteins, including PYR1, PyR1-like protein (PYL), and ABA receptor regulatory component (RCAR), simultaneously accumulate ABA in response to salt stress, thereby inhibiting the phosphatase activity of PP2C. In addition, the kinase activity of SnRK2.4 activated by salt stress is inhibited by ABI1 and acid-sensitive phosphatases of the phosphoprotein phosphatase (PPP) family. It has been concluded that, under the influence of salt stress, ABA is accumulated, which activates SnRK2.4 and inhibits type 2C PP2CA protein phosphatase and ABI1, thus regulating the plants' response to salt stress [43]. In addition, ABA can regulate plant tolerance to stress by regulating stomatal closure. Under exposure to stress, the increase in ABA content activates SnRK2.6/OST1, a key regulator of Ca 2+ -independent stomatal closure, and OST1 activates SLAC1, KUP6, and QUAC1. The exosmosis of Cl − , K + , and Malate 2− is further promoted, whereas internal K + transport is reduced. Ultimately, ABA regulates plant adaptation to stress by inducing stomatal closure through ion flux in the guard cells [44]. Under drought stress, the ABA content in plants will increase, which will induce stomatal closure to regulate water loss. In A. thaliana, AtNCED3 is a crucial gene for ABA synthesis [45]. AtNCED3 is mainly expressed in the vascular bundles of leaves [46]. The synthesis and accumulation of ABA in the leaves has a regulatory effect on stomatal closure, and thus increases the salt tolerance of plants.
Transformation with MbMYB4 improves the tolerance of transgenic A. thaliana plants to cold stress [47]. In the present study, WT, UL, and FvMYB82-transgenic A. thaliana lines (L1, L3, and L5) suffered damage under low temperature and high salt stress, but the transgenic lines showed less severe yellowing, and growth was restored after they were transferred to a non-stress environment. The percentage survival of the transgenic lines was significantly higher than that of the WT and UL plants. These results showed that FvMYB82 significantly improved the resilience of A. thaliana to low temperature and high salt stress. To examine the mechanism by which FvMYB82 improved the stress tolerance of A. thaliana, physiological indicators and downstream gene expression of stress-treated A. thaliana lines were analyzed.
Proline is an important osmotic regulator of plant cells, which can change the osmotic concentration of cells, reduce the freezing point, and increase the cold tolerance of plants [48]. Under low-temperature stress, osmotic regulators such as proline will accumulate rapidly in plants [49]. The accumulation of proline increases the water retention of cells, promotes hydrin formation, and increases the content of soluble protein in cells, so that plants can better resist the effects of low temperature. The proline content of the transgenic A. thaliana lines (L1, L3, and L5) was increased under cold stress, indicating that the transgenic lines had better water retention than the WT and UL, and a superior ability to withstand cold stress. Chlorophyll is an important indicator of the cold tolerance of plants. A low temperature will result in chlorophyll degradation in the leaves, causing yellowing and disruption of photosynthesis [50]. Under low-temperature stress, the leaves of the transgenic lines (L1, L3, and L5) showed less severe yellowing, whereas the leaves of the WT and UL experienced more severe yellowing. Thus, the chlorophyll content in the transgenic lines was higher than that in the WT and UL under cold stress. These results indicated that the transgenic lines could more effectively resist chlorophyll decomposition at a low temperature. Oxidative products produced by plants in response to low temperature and high salt stress are removed by the reactive oxygen species scavenging system, which includes SOD, CAT, and POD, so as to avoid oxidative damage and improve stress tolerance [51]. The POD and CAT activities in rice roots under cold stress are significantly increased compared with those in non-stressed rice [52]. In the present study, compared with the WT and UL, A. thaliana overexpressing FvMYB82 had higher activities of CAT, POD, and SOD, and lower contents of MDA under cold stress. These results indicate that transgenic A. thaliana has better antioxidant ability and less damage to plants at low temperature.
MYB gene can bind to CBF promoter, thereby promoting the expression of various downstream genes associated with cryogenic stress, inhibiting CBFs response, and further negatively regulating the tolerance of plants to low-temperature stress [53][54][55]. In addition, the crucial genes responsive to the CRT/DRE pathway, such as CORs, RDs, LTIs, and other cis-acting elements, can be induced by CBFs, thus positively enhancing the ability of plants to cope with cold stress. MYB transcription factors can also negatively regulate freezing tolerance. For example, MYB15 functions as a negative signaling regulator and is degraded by PUB25 and PUB26, the targets of the protein kinase OST1. Low temperature activates OST1 to phosphorylate PUB25 and PUB26, which enhances their activity, and promotes the ubiquitination and degradation of MYB15, thus positively inducing expression of ICE1 and CBFs at low temperature [56][57][58][59]. In this study, FvMYB82 positively regulates cold tolerance through two key genes AtCBF1 and AtCBF2, as well as the expression of downstream cold responsive genes AtCOR15a and AtCOR78.
Based on the above results and former studies, we made a potential model to describe the role of FvMYB82 in salt and cold stresses ( Figure 11). The expression levels of SnRK family genes (SnRK2.4 and SnRK2.6), AtNCED3 and AtKUP6 increased obviously in transgenic (L1, L3 and L5) A. thaliana compared with WT and UL lines under salt stress, indicating that FvMYB82 could promote downstream salt-stress-related gene expression and positively regulate the ABA biosynthesis and signal transduction pathway to improve the slat tolerance of plants. ABA and drought stress increased SsMYB113 transcription, further improving expression of the corresponding biosynthetic genes SsNCED in overexpressed SsMYB113 A. thaliana lines. At the same time, ROS of SsMYB113-OE were modulated to regulate drought stress tolerance [60]. For this, we proposed that the enzyme of transgenic plant was modulated by ABA signal to improve the abiotic stress tolerance in the hypothesis model. Meanwhile, in the cold environment, the CBF family genes (CBF1 and CBF2), COR15a and COR78 expression levels were higher in transgenic (L1, L3, and L5) A. thaliana than in WT and UL, indicating that the cold stress could induce the expression of FvMYB82, and FvMYB82 domain binding to the promoter regions of CBF1 and CBF2 and promote binding of CBFs to the CRT/DRE cis-acting elements of downstream genes, thereby activating expression of the downstream cold-responsive genes COR15a and COR78, finally enhancing plant cold tolerance. positively regulate the ABA biosynthesis and signal transduction pathway to improve the slat tolerance of plants. ABA and drought stress increased SsMYB113 transcription, further improving expression of the corresponding biosynthetic genes SsNCED in overexpressed SsMYB113 A. thaliana lines. At the same time, ROS of SsMYB113-OE were modulated to regulate drought stress tolerance [60]. For this, we proposed that the enzyme of transgenic plant was modulated by ABA signal to improve the abiotic stress tolerance in the hypothesis model. Meanwhile, in the cold environment, the CBF family genes (CBF1 and CBF2), COR15a and COR78 expression levels were higher in transgenic (L1, L3, and L5) A. thaliana than in WT and UL, indicating that the cold stress could induce the expression of FvMYB82, and FvMYB82 domain binding to the promoter regions of CBF1 and CBF2 and promote binding of CBFs to the CRT/DRE cis-acting elements of downstream genes, thereby activating expression of the downstream cold-responsive genes COR15a and COR78, finally enhancing plant cold tolerance.

Plant Materials, Growth Conditions, and Treatment
The diploid F. vesca seedlings were cultured on Murashige and Skoog (MS) medium supplemented with 0.6 mg/L indole-3-butyric acid (IBA) and 0.6 mg/L 6-benzylaminopurine (6BA) or in soil in an incubator under a 16 h/8 h (light/dark) photoperiod and 70% relative humidity at 22 °C at the College of Horticulture and Landscape Architecture, Harbin, China. Seeds of A. thaliana ecotype Columbia-0 were obtained from the A. thaliana Biological Resource Center (https://abrc.osu.edu/, Ohio State University, USA (accessed on 16 October 2019) ). A. thaliana seedlings cultured in an incubator under the same conditions as wild strawberry. For low-temperature treatment, strawberry seedlings were grown in an incubator at 4 °C. To test the drought, salt, and ABA stress tolerances, the seedlings were treated with 15% PEG6000, 200 mM NaCl, or 100 μM ABA, respectively [61]. F. vesca materials treated with abiotic stresses were sampled at different time intervals (0, 1, 2, 4, 6, 8, and 12 h). The collected immature leaves, mature leaves, stems, and roots were quickly frozen with liquid nitrogen and stored at −80 °C for tissue-specific gene expression analysis [62].

Plant Materials, Growth Conditions, and Treatment
The diploid F. vesca seedlings were cultured on Murashige and Skoog (MS) medium supplemented with 0.6 mg/L indole-3-butyric acid (IBA) and 0.6 mg/L 6-benzylaminopurine (6BA) or in soil in an incubator under a 16 h/8 h (light/dark) photoperiod and 70% relative humidity at 22 • C at the College of Horticulture and Landscape Architecture, Harbin, China. Seeds of A. thaliana ecotype Columbia-0 were obtained from the A. thaliana Biological Resource Center (https://abrc.osu.edu/, Ohio State University, USA (accessed on 16 October 2019)). A. thaliana seedlings cultured in an incubator under the same conditions as wild strawberry. For low-temperature treatment, strawberry seedlings were grown in an incubator at 4 • C. To test the drought, salt, and ABA stress tolerances, the seedlings were treated with 15% PEG6000, 200 mM NaCl, or 100 µM ABA, respectively [61]. F. vesca materials treated with abiotic stresses were sampled at different time intervals (0, 1, 2, 4, 6, 8, and 12 h). The collected immature leaves, mature leaves, stems, and roots were quickly frozen with liquid nitrogen and stored at −80 • C for tissue-specific gene expression analysis [62].

Isolation and Cloning of FvMYB82
Total RNA was extracted from the F. vesca materials (immature and mature leaves, stems, and roots) using the OminiPlant RNA Kit (Conway Collection, Beijing, China) following the manufacturer's instructions. The TransScript First-Strand cDNA Synthesis SuperMix (TransGen Biotech, Beijing, China) was used to synthesize the first-strand cDNA. Agarose gel (1%) electrophoresis was used to analyze and verify the RNA and cDNA. The coding sequence of F. vesca FvMYB82-like (XM_004288737.2) was used as the reference sequence to amplify the full-length cDNA sequence, and gene-specific primers (FvMYB82-F and FvMYB82-R; Table S1) were designed with Primer 5.0 software. The PCR product fragments were purified and ligated into the ASY-T1 vector (TransGen Biotech, Beijing, China) for sequencing [35].

Subcellular Localization of FvMYB82
The coding region of FvMYB82 was amplified and inserted into the pSAT6-GFP-N1 vector to generate fusion proteins with the green fluorescence protein (GFP). The upstream and downstream primers (FvMYB82-slF and FvMYB82-slR; Table S1) together with SalI and BamHI restriction enzymes were used to obtain FvMYB82 gene fragments. SalI and BamHI acted as double-digestion restriction enzymes to digest the PCR product and the pSAT6-GFP-N1 vector. The FvMYB82 fusion plasmid containing the target fragment was then inserted into onion 'Yachunya57 outer epidermal cells using the particle bombardment method. The empty 35S::GFP vector was used as a control [63]. The subcellular expression of the FvMYB82-GFP fusion protein was observed with a confocal microscope (Olympus Corporation, Tokyo, Japan). DAPI staining was used as a nucleus marker for nucleus detection.

Sequence Analysis and Structure Prediction of FvMYB82
In order to achieve multiple sequence alignment of FvMYB82 and other species of MYB TFs, DNAMAN 5.2 was performed. The phylogenetic tree was constructed using a neighbor-joining method [64] with MEGA7 (available online: http://www.megasoftware. net (accessed on 1 June 2022)) [65]. To predict the primary structure of FvMYB82 protein, ExPASy was used as a tool (available online: https://web.expasy.org/protparam/(accessed on 1 June 2022)). Using SMART (SMART: Main page. Available online: http://smart. embl-heidelberg.de/ accessed on 1 June 2022) website to predict the domain of FvMYB82 protein, the tertiary structure of FvMYB82 protein was predicted on the SWISS-MODEL website (SWISS-MODEL. Available online: https://swissmodel.expasy.org/ accessed on 1 June 2022) [66].

Expression Analysis of FvMYB82
The qPCR (Table S1) was used to detect the expression levels of FvMYB82 under multiple abiotic stresses in different tissues using the primers FVMYB82-qF and FVMYB82-qR (Table S1). The PCR protocol was as follows: 30 s at 94 • C; then 40 cycles of 5 s at 95 • C, 40 s at 54 • C, and 30 s at 72 • C; and 10 min at 72 • C. The expression of the FvMYB82 gene was detected with the TB Green™ Premix Ex Taq™ II (Tli RNaseH Plus kit) (TaKaRa, Beijing, China) in accordance with the manufacturer's protocol [67]. The Actin gene (XM_011471474.1, F. vesca) was used as the internal reference gene. The FvMYB82 expression level was calculated using the 2 −∆∆Ct method.

Stress Treatment and Determination of Related Physiological Indexes in A. thaliana
For the germination rate, A. Thaliana wild-type (WT), no-load system (UL) and T3 transgenic lines (L1, L3, L5) were divided into two groups, respectively. For cold treatment, one group was planted in 1/2 MS medium, after being vernalized in a 4 • C refrigerator for two days. The Petri dish was cultured in a −6 • C refrigerator. The other group was planted in a Petri dish with filter paper for salt treatment, and 10 mL 200 mM NaCl solution was added to one dish. After being vernalized at 4 • C, these Petri dishes were transferred into a light incubator, with 50 seeds per line, three replicates every treatment. Germination was observed after one week.
For related Physiological Indexes in A. thaliana, wildtype (WT), empty vector line (UL) and T3 transgenic lines (L1, L3, L5) of A. thaliana were planted in1/2 MS medium for 10 days. When cotyledons showed, the seedlings were transferred to nutrient pots containing a substance including soil and vermiculite (2:1) (4 plants per pot). Every line of A. thaliana was divided into two groups: one group was treated with salt stress (irrigating 200 mM NaCl for 7 days), and then water for 3 days for recovery. The other group was treated with cold stress (14 h, −6 • C), and later cultured in normal condition for 7 days for recovery. Morphological characteristics were observed, and the percentage survival was determined [68].
All materials of each line treated with different stress and CK were collected for a physiological indexes test. The fresh leaf samples were soaked in the mixture of ethanol and acetone for 24 h, and then the absorbance of the mixture at 645 nm and 663 nm was measured using a spectrophotometer, which was used to calculate the content of chlorophyll [69]. The content of MDA was determined according to the reaction of MDA with thiobarbituric acid under acidic and high temperature conditions to generate redbrown trimethyloxazole, and the maximum absorption peak was at 532 nm. [70]. Refer to the method of Huang et al. the content of proline was determined by sulfosalicylic acid method [71][72][73]. The activity of SOD was determined according to its inhibition of NBT reduction under light. [74], In the presence of hydrogen peroxide, POD can oxidize guaiacol to produce a brown color, and the product can be determined by a spectrophotometer. [75] Catalase can decompose hydrogen peroxide so that the absorbance (A240) of reaction solution decreases with the reaction time. Catalase activity can be measured according to the change rate of absorbance. [76]. We measured the conductance of the extract solution with a conductivity meter, heated it in a boiling water bath for 30 min, cooled it down sufficiently, measured the conductance again, and used the formula to calculate the EL [77].

Expression Analysis of Genes Associated with Salt Tolerance in FvMYB82-OE A. thaliana
Using AtActin as an internal reference, the total mRNAs were extracted from untreated (CK) and salt-treated A. thaliana lines (WT, UL, L1, L3, and L5). The cDNA was used as a template for reverse transcription of the first-strand cDNA. The expression levels of four salt stress-responsive genes (AtSnRK2.4, AtSnRK2.6, AtKUP6, and AtNCED3) located downstream of MYB transcription factors were quantified by qPCR analysis [78,79]. The specific primers used are listed in Table S1. The procedure followed the reaction system described in Section 4.5.

Expression Analysis of Cold-Tolerance-Related Genes in A. thaliana Overexpressing FvMYB82
Using AtActin as an internal reference, the total mRNAs were extracted from untreated (CK) and low-temperature-treated A. thaliana lines (WT, UL, L1, L3, and L5). The cDNA was used as a template for reverse transcription of the first-strand cDNA. Four coldresponsive genes (AtCBF1, AtCBF2, AtCOR15a, and AtCOR78) located downstream of MYB transcription factors were quantified by qPCR analysis. The gene-specific primers used are listed in Table S1. The procedure followed the reaction system described in Section 4.5.

Statistical Analysis
SPSS 21.0 software (IBM, Chicago, IL, USA) was used to analyze the differences via Duncan's multiple range tests. The bars showed the mean and standard deviation (SD) of three replicates. Statistical differences were referred to as significant when * p ≤ 0.05 and ** p ≤ 0.01.

Conclusions
In this study, FvMYB82 of F. vesca was identified and cloned. Overexpression of FvMYB82 significantly enhanced the tolerance of A. thaliana to abiotic stress. The activities of the antioxidant enzyme system were significantly increased, and the membrane-lipid stability and ROS homeostasis were maintained under salt and cold stress. Meanwhile, the morphogenesis of A. thaliana seedlings was altered to improve the resistance to stress. The present results show that FvMYB82 plays a very important role in plants' response to low temperature and salt stresses.