Multiple Functions of MYB Transcription Factors in Abiotic Stress Responses

Plants face a more volatile environment than other organisms because of their immobility, and they have developed highly efficient mechanisms to adapt to stress conditions. Transcription factors, as an important part of the adaptation process, are activated by different signals and are responsible for the expression of stress-responsive genes. MYB transcription factors, as one of the most widespread transcription factor families in plants, participate in plant development and responses to stresses by combining with MYB cis-elements in promoters of target genes. MYB transcription factors have been extensively studied and have proven to be critical in the biosynthesis of secondary metabolites in plants, including anthocyanins, flavonols, and lignin. Multiple studies have now shown that MYB proteins play diverse roles in the responses to abiotic stresses, such as drought, salt, and cold stresses. However, the regulatory mechanism of MYB proteins in abiotic stresses is still not well understood. In this review, we will focus mainly on the function of Arabidopsis MYB transcription factors in abiotic stresses, especially how MYB proteins participate in these stress responses. We also pay attention to how the MYB proteins are regulated in these processes at both the transcript and protein levels.


Introduction
MYB transcription factors represent one of the largest protein families in plants. MYB transcription factors are characterized by highly conserved N-terminal MYB DNA-binding domain (DBD) repeats (Rs). Each repeat contains approximately 52 amino acid residues that fold into three α-helices. The second and third helices can form a helix-turn-helix (HTH) structure. Due to the similarity with the c-Myb protein, these repeats are renamed R1, R2, and R3. In plants, MYB transcription factors comprise one to four DNA-binding repeats. However, the majority of MYB proteins contain two repeats and belong to the R2R3-MYB subfamily. Many plant species encode more than 100 R2R3 MYB proteins. In contrast to the N-terminus, the C-terminal region is more variable and responsible for regulatory function. For example, in Arabidopsis, 126 R2R3 MYB proteins can be divided into 23 subgroups based on the conserved region of the C-terminus [1,2].
R2R3-MYB proteins have been found to participate in diverse processes, including primary and secondary metabolism, plant development, and responses to biotic and abiotic stresses [1]. Among these functions, MYB proteins have been particularly well studied as regulators of phenylpropanoid metabolism, such as the biosynthesis of proanthocyanidins (PAs), anthocyanins, flavonols, and lignin in plants. For example, MYB proteins can bind to the bHLH transcription factor and WD40 protein to form the MBW complex and activate the biosynthesis of PAs and anthocyanins [3][4][5][6]. Multiple studies have indicated the critical roles of MYB transcription factors in plant stress responses, especially in abiotic stresses [7][8][9]. In this review, we will describe the function of Arabidopsis R2R3 MYB proteins in abiotic stress responses, focusing mainly on their roles in drought, high salinity,

Flavonoid and Cuticle Biosynthesis with Drought Tolerance
First, MYB proteins, as one of the most important transcription factor families in plant metabolism biosynthesis, participate in drought tolerance related to the leaf permeability, by regulating the synthesis of flavonoids and cuticle.
Flavonoids represent a major component of the secondary metabolism in plants and comprise several major subgroups, including flavones, flavonols, anthocyanins, and proanthocyanidins. Flavonoids have been extensively described as defense metabolites for their role as antioxidants in protecting the plant from biotic and abiotic stresses by scavenging ROS [21]. MYB transcription factors in Arabidopsis have been demonstrated to be key regulators of flavonoid biosynthesis [22]. MYB12 upregulates the expression of the early flavonol biosynthetic genes CHS (chalcone synthase) and FLS (flavonol synthase), whereas the anthocyanin regulators MYB75/PAP1 control the expression of the late biosynthetic genes DFR (dihydroflavonol reductase) and LDOX/ANS (leucoanthocyanidin dioxygenase/anthocyanidin synthase) [23,24]. Overexpression of MYB12 and MYB75 in transgenic plants significantly increased the accumulation of flavonoids with strong antioxidant activity, thus leading to enhanced tolerance to abiotic stresses such as drought and oxidative stresses [22,25].
The cuticle is one of the most important plant structures and protects aerial plant organs from desiccation [26]. The main components of the cuticle contain cutin and wax, the biosynthesis of which is widely regulated by MYB transcription factors. In Arabidopsis, MYB41 negatively regulates the expression of cutin synthesis genes; MYB30, MYB94, and MYB96 function as positive regulators of wax synthesis genes, while MYB16 together with MYB106 can activate the synthesis of both cutin and wax [27]. Among these transcription factors, MYB41, MYB94, and MYB96 have been found to be involved in the drought response. Drought induction of cuticular wax biosynthetic genes requires the expression of MYB94 and MYB96. MYB94 and MYB96 additively activate cuticular wax biosynthesis in response to drought by directly promoting the expression of the same wax biosynthetic genes. Overexpression of MYB96 leads to the upregulation of cuticular wax biosynthesis, thus contributing to drought tolerance in both Arabidopsis and Camelina sativa. Although

Flavonoid and Cuticle Biosynthesis with Drought Tolerance
First, MYB proteins, as one of the most important transcription factor families in plant metabolism biosynthesis, participate in drought tolerance related to the leaf permeability, by regulating the synthesis of flavonoids and cuticle.
Flavonoids represent a major component of the secondary metabolism in plants and comprise several major subgroups, including flavones, flavonols, anthocyanins, and proanthocyanidins. Flavonoids have been extensively described as defense metabolites for their role as antioxidants in protecting the plant from biotic and abiotic stresses by scavenging ROS [21]. MYB transcription factors in Arabidopsis have been demonstrated to be key regulators of flavonoid biosynthesis [22]. MYB12 upregulates the expression of the early flavonol biosynthetic genes CHS (chalcone synthase) and FLS (flavonol synthase), whereas the anthocyanin regulators MYB75/PAP1 control the expression of the late biosynthetic genes DFR (dihydroflavonol reductase) and LDOX/ANS (leucoanthocyanidin dioxygenase/anthocyanidin synthase) [23,24]. Overexpression of MYB12 and MYB75 in transgenic plants significantly increased the accumulation of flavonoids with strong antioxidant activity, thus leading to enhanced tolerance to abiotic stresses such as drought and oxidative stresses [22,25].
The cuticle is one of the most important plant structures and protects aerial plant organs from desiccation [26]. The main components of the cuticle contain cutin and wax, the biosynthesis of which is widely regulated by MYB transcription factors. In Arabidopsis, MYB41 negatively regulates the expression of cutin synthesis genes; MYB30, MYB94, and MYB96 function as positive regulators of wax synthesis genes, while MYB16 together with MYB106 can activate the synthesis of both cutin and wax [27]. Among these transcription factors, MYB41, MYB94, and MYB96 have been found to be involved in the drought response. Drought induction of cuticular wax biosynthetic genes requires the expression of MYB94 and MYB96. MYB94 and MYB96 additively activate cuticular wax biosynthesis in response to drought by directly promoting the expression of the same wax biosynthetic genes. Overexpression of MYB96 leads to the upregulation of cuticular wax biosynthesis, thus contributing to drought tolerance in both Arabidopsis and Camelina sativa. Although the myb94 mutant showed a phenotype similar to the wild type, the water loss rate of the myb94 myb96 double mutant through the cuticle was faster, suggesting the additive role of MYB94 with MYB96 [28][29][30][31]. MYB41 negatively regulated the expression of the cutin synthesis genes ATT1 and LACS2. Similarly to other cuticle biosynthesis mutants, the MYB4 overexpression plants exhibited a dwarf appearance, with smaller cells, and were characterized by an abnormal morphology. The expression of MYB41 can be significantly induced in response to desiccation and ABA. Transgenic plants also show hypersensitivity to desiccation due to the enhanced permeability of leaf surfaces [32].

Light and ABA-Mediated Stomatal Movement
Plants use stomata on the epidermis to exchange carbon dioxide and water with the atmosphere. Regulation of the stomatal aperture is one of the most important ways for plants to control water loss [33]. Arabidopsis MYB transcription factors have been found to be widely involved in the drought response via stomatal movement. MYB60 is the first transcription factor shown to participate in the regulation of stomatal movement. MYB60 is specifically expressed in guard cells, and its expression is induced by signals such as white and blue light that promote stomatal opening, but repressed by signals that promote stomatal closure, such as darkness, desiccation, and ABA treatment. Lightinduced stomatal opening was repressed in the myb60 mutant, thus enhancing plant drought tolerance via less water loss [34]. Conversely, MYB60 overexpression plants exhibited hypersensitivity to drought stress [35].
The other MYBs found so far mainly rely on ABA signals to participate in the regulation of plant stomatal movement. AtMYB44 is highly expressed in guard cells. However, its role in drought tolerance is controversial. Jung et al. [36] revealed that overexpression of MYB44 led to enhanced ABA sensitivity in both germination and stomatal closure, resulting in increased drought tolerance. Jaradat et al. [37] demonstrated that AtMYB44 negatively regulated ABA signaling. The involvement of MYB44 in ABA signaling seems to occur through the regulation of the ABA receptor RCARs/PYR1/PYLs. MYB44 can interact with RCAR3/PYL8 and RCAR1/PYL9 [37,38]. MYB44 competes with ABI1 to bind to RCAR1/PYL9, thus releasing the inhibitory effect of RCAR1/PYL9 on ABI1 phosphatase activity [38]. AtMYB77 can interact with MYB44 to form a heterodimer and additively function with MYB44 under drought stress. The myb44 myb77 double mutants exhibited stronger drought tolerance [36]. MYB77 can also interact with RCAR3/PYL8 and RCAR1/PYL9 [37,38]. The PYL8-MYB77 interaction enhanced MYB77 activity to induce the expression of multiple auxin-responsive genes, thus promoting lateral root growth [39].
Despite wax synthesis, MYB96 also regulates drought resistance through the ABA signaling pathway. When expressed in leaves, MYB96 is localized mainly to guard cells. The stomatal aperture is more sensitive to ABA and drought in AtMYB96-overexpression plants but less sensitive in myb96 null mutants. The myb96 mutant showed a more susceptible phenotype in its drought response [40]. Lipid transfer protein 3 works as a target of MYB96 in ABA signaling to modulate MYB96-mediated drought tolerance. MYB96 positively regulates the expression of LTP3 via direct binding to its promoter. The ltp3 null mutant is less sensitive to drought stress, whereas overexpression of LTP3 can restore the hypersensitivity of the myb96 mutant to drought stress [41]. MYB96 can also negatively regulate a subset of ROP genes, which act as negative regulators of multiple ABA responses, including stomatal closure and drought responses, via the histone modifier HDA15. hda15 null mutants exhibited reduced ABA sensitivity and were more susceptible to drought stress than the myb96 mutant. MYB96 can interact with HDA15 and recruit HDA15 to the promoters of ROP6, ROP10, and ROP11, thus repressing their expression by removing acetyl groups of histone H3 and H4 from the cognate regions [42].
Arabidopsis FLP (FOUR LIPS; MYB124) and its closest homolog MYB88 are critical for the formation of stomata. Stomata are developed from GMCs (guard mother cells), which divide symmetrically to produce two cells of equal size and fate. FLP is expressed late in the stomatal cell lineage to restrict cell divisions before terminal differentiation. FLP prevents new GMC daughter cells from perpetuating divisions, to restrict GMCs to a single division.
In the flp mutant, GMCs undergo more than one round division, resulting in the formation of stomatal clusters. Mutations in MYB88 showed no stomatal phenotype, but flp myb88 double mutants exhibited larger stomatal clusters than flp alone, indicating an additive role of MYB88 with FLP. As transcription factors, FLP and MYB88 can repress the expression of the mitosis-inducing factor CDKB1;1, which is specifically required for the last division in the stomatal pathway by directly binding to its promoter. However, the mutation of cdkb1;1 can repress stomatal clusters of flp myb88 double mutants [43,44]. FLP and MYB88 are also involved in ABA-mediated stomatal movement. ABA-induced stomatal closure is significantly repressed in flp myb88 double mutants, resulting in the mutant having a phenotype more susceptible to drought stresses. Additionally, FLP and MYB88 control the drought stress response partially by regulating the expression of the NAC transcription factor, NAC019. The expression of NAC019 is induced by drought, and overexpression of NAC019 can increase plant drought tolerance. FLP and MYB88 directly activate NAC019 gene expression to promote the expression of downstream stress-responsive genes [45,46].
At the same time, there are still many other MYB proteins involved in the ABAmediated stomata closure, but their functions are not yet clear. MYB20 functions as a negative regulator of ABA-mediated stomatal closure. The expression of MYB20 is suppressed by desiccation and ABA treatment. Stomatal closure is insensitive to ABA in MYB20-overexpressing plants but sensitive in MYB20 knockout mutations. Thus, overexpression of MYB20 plants showed increased susceptibility to desiccation, and myb20 null mutants exhibited enhanced resistance to desiccation [47]. MYB15 and MYB37 play a positive role in the plant response to ABA and drought stress. The expression of MYB15 and MYB37 can be strongly induced by ABA. Overexpression of MYB15 and MYB37 improves plant tolerance to drought by promoting ABA-induced stomatal closure [48,49].

MYBs in Regulation of ABA Signaling
ABA plays critical roles in plant responses to abiotic stresses and is also involved in multiple physiological processes, such as seed germination and dormancy, osmotic regulation, and leaf senescence [50]. In addition to ABA-mediated stomatal closure, many MYB transcription factors also participate in other ABA-regulated signaling pathways. For example, MYB15, MYB37, and MYB96 are also involved in ABA-mediated seed germination repression, while MYB77 and MYB96 modulate lateral root development in response to ABA [7,40,48,49]. Additionally, there are many MYB proteins that have been identified to be involved in the ABA signaling pathway. AtMYB2 participates in ABA-mediated seed germination through the regulation of the expression of the RD22 and miRNA gene, miR399f. MYB2 positively regulates the expression of RD22, which is a dehydration-responsive gene induced by the application of exogenous ABA, by binding to the promoter of RD22. MYB2 is induced by drought and ABA treatment, and overexpression of MYB2 causes hypersensitivity to ABA during germination [51]. MYB2 also activates the expression of miR399f by directly binding to a MYB-binding motif in its promoter [52]. The expression of miR399f can also be induced by ABA treatment, and plants overexpressing miR399f exhibited a hyposensitive phenotype in response to ABA during seed germination and root growth but hypersensitivity to drought stress [53]. MYB33 and MYB101 have been identified as positive regulators of ABA signaling during germination. Null mutants of myb33 and myb101 showed hyposensitivity to ABA. However, their function in ABA signaling is still not clear. Meanwhile, MYB33 and MYB101 have been identified as targets of miR159 (microRNA 159). miR159 mediates the cleavage of MYB101 and MYB33 transcripts. Overexpression of miR159 can suppress the expression of MYB33 and MYB101, thus rendering plants hyposensitive to ABA. Furthermore, ABA induced the accumulation of miR159 in germinating seeds, miR159-mediated MYB33, and MYB101 transcript degradation seems to act as a negative feedback regulation to finetune ABA signaling during seed germination [54]. Plants overexpressing MYB52 showed hypersensitivity to ABA during postgermination and root growth, and enhanced drought tolerance with higher survival rates under desiccation, suggesting that MYB52 is a positive regulator of ABA signaling [55].
In contrast, MYB7 and MYB30, which are involved in cuticle synthesis, act as negative regulators in ABA signaling. MYB7 negatively regulates ABA-induced inhibition of seed germination by blocking the expression of ABI5. Compared to the wild type, the ABI5 expression is much higher in myb7 mutant, and thus leading to hypersensitivity to ABA during seed germination [56]. MYB30 was first identified as the key positive regulator of HR (hypersensitive response) by modulating the synthesis of VLCFAs (very-long-chain fatty acids), the components of cuticular wax. MYB30 also belongs to the S1 subgroup with MYB96 and MYB94. However, unlike MYB96, MYB30 negatively regulates ABA signaling in seeds, as myb30 null mutants exhibited hypersensitivity to ABA during seed germination and postgermination growth. However, the myb30 mutant showed no differences compared to the wild type under drought stress. Considering that MYB30 can interact with MYB96 and their opposite roles in ABA signaling, MYB30 may participate in the regulation of ABA signaling through a complex regulatory network [40,57,58].

MYBs Modulate Salt Tolerance
Salt stress is one of the major environmental factors that limits plant growth and productivity. Salt stress can lead to ionic stress, osmotic stress, and secondary stresses, especially oxidative stress [59]. MYB proteins also contribute to plant salt tolerance and many of their downstream targets have been identified (Figure 2). MYB49 positively modulates salt tolerance by modulating cuticle formation and antioxidant defense. The null mutant of MYB49 displayed higher electrolyte leakage and less tolerance to salt stress, while overexpression of MYB49 improved salt tolerance. MYB49 was found to activate the expression of cutin, suberin, and wax biosynthetic genes such as MYB41, ASFT, FACT, and CYP86B1 by directly binding to their promoters. Meanwhile, MYB49 can elevate Ca 2+ levels in leaves and improve antioxidant capacity by upregulating genes encoding peroxidases and late embryogenesis abundant proteins [60].   [36,61]. MYB42 enhanced the expression of SOS2 to facilitate Na + efflux, while MPK4 phosphorylates MYB42 to protect it from degradation under salt stress [62]. MYB30 activates AOX1a expression to keep cellular redox homeostasis and MYB49 modulates cuticle formation and antioxidant defense [60,63]. Besides its role in flavonoids and cuticle formation, MYB12 can also induce the expression of ABA biosynthesis genes to confer plant salt tolerance [25].
MYB30 modulates plant salt tolerance through the regulation of mitochondrial alternative oxidase AOX1a (alternative oxidase 1a). MYB30 mutants exhibited hypersensitivity to salt stress. In response to salt stress, MYB30 directly binds to the promoter of AOX1a to  [36,61]. MYB42 enhanced the expression of SOS2 to facilitate Na + efflux, while MPK4 phosphorylates MYB42 to protect it from degradation under salt stress [62]. MYB30 activates AOX1a expression to keep cellular redox homeostasis and MYB49 modulates cuticle formation and antioxidant defense [60,63]. Besides its role in flavonoids and cuticle formation, MYB12 can also induce the expression of ABA biosynthesis genes to confer plant salt tolerance [25].
Many MYB proteins involved in the ABA response also participate in regulating salt tolerance through the regulation of genes in ABA signaling. The expression of MYB20 can be induced by NaCl treatment, and overexpression of MYB20 enhanced salt stress tolerance. MYB20 negatively regulates the expression of PP2Cs, the major negative regulators of ABA signaling, by directly binding to their promoters, thus leading to salt tolerance in plants [61]. MYB44 also participates in the salt response through the regulation of PP2Cs. Salt-induced activation of PP2C genes, such as ABI1, ABI2, AtPP2CA, HAB1, and HAB2 was diminished in MYB44-overexpressing plants, but enhanced in the myb44 mutant. Overexpression of MYB44 can enhance tolerance to salt stress [36]. MYB7 participates in salt stress during seed germination though the negative regulation of ABI5. Mutation of MYB7 can cause hypersensitivity to salt stress during seed germination [56].
MYB42 positively modulates salt tolerance through the regulation of SOS2 (salt overly sensitive 2) expression. SOS2 encodes a serine/threonine protein kinase and activates Na + /H + exchanger SOS1 through phosphorylation, thus facilitating Na + efflux for enhancing plant salt tolerance. The myb42 mutant exhibited enhanced salt sensitivity, while MYB42-overexpression lines improved salt tolerance compared with the wild type. MYB42 activates the expression of SOS2 gene by directly binding to SOS2 promoter, thus inducing its expression under salt stress. MPK4 (mitogen-activated protein kinase 4) participates in salt tolerance through the regulation of MYB42. NaCl treatment can enhance the interaction of MPK4 with MYB42, thus leading to the phosphorylation of MYB42. Salt treatment can induce the degradation of MYB42. This phosphorylation enhances the stability of MYB42 under salt-stress conditions [62].
MYB30 modulates plant salt tolerance through the regulation of mitochondrial alternative oxidase AOX1a (alternative oxidase 1a). MYB30 mutants exhibited hypersensitivity to salt stress. In response to salt stress, MYB30 directly binds to the promoter of AOX1a to promote its expression, thus maintaining the cellular redox homeostasis through enhanced Alt respiration. Overexpression of AOX1a can rescue the myb30 salt-sensitive phenotype [63]. In addition to flavonoid biosynthesis and ROS scavenging, overexpression of MYB12 also upregulated the expression of genes involved in ABA and proline biosynthesis, thus conferring salt tolerance to the plants [22,25].
Besides the targets of MYB proteins, how MYBs are regulated in salt stress is revealed by the study of MYB74. MYB74 plays a positive role in the salt response. NaCl treatment can induce the expression of MYB74. Transgenic plants overexpressing MYB74 displayed hypersensitivity to NaCl during seed germination. Further analysis showed that the expression of MYB74 in response to salt stress is under the control of the RdDM (RNAdirected DNA methylation) pathway. Twenty-four-nt siRNAs target a region approximately 500 bp upstream of the transcription initiation site of MYB74. This target site for siRNA is essential for maintaining MYB74 expression patterns and has been shown to be heavily methylated via the RdDM pathway. Salt stress induces the expression of MYB74 by repressing the accumulation of 24-nt siRNAs and the RdDM pathway [64].
In addition to the above genes, many other MYB proteins are also involved in the salt tolerance response. For example, transgenic plants overexpressing MYB41 showed enhanced salt tolerance on germination and root growth. MYB15 overexpression lines displayed improved salt stress tolerance [48]. myb108 and flp myb88 mutant plants were significantly more susceptible to high salt during seed germination [45,65]. In contrast, MYB52 negatively regulates plant salt tolerance, and overexpression of MYB52 causes hypersensitivity to salt stress on seed germination [55]. However, their functions in salt stress still need to be investigated.

MYBs Serve as Repressors in Cold and Heat Tolerance
Cold stress threatens the growth and development of plants by greatly affecting plant metabolism and transcriptomes. Cold stress rapidly induces the expression of CBFs (C-repeat-binding factors), the key transcription factors in the cold response, in order to activate the expression of numerous downstream COR (cold-responsive) genes [66]. MYB transcription factors are considered to play critical roles in cold tolerance because of their regulation of CBF genes. Among them, AtMYB15 has been identified as the key regulator of CBF genes in response to low temperature. The expression of MYB15 can be induced by cold stress. The myb15 mutant plants showed increased tolerance to freezing stress, whereas the overexpression plants exhibited reduced freezing tolerance. MYB15 repressed the expression of CBF genes by directly binding to MYB binding sites in their promoters. Cold-induced CBF expression was reduced in MYB15-overexpressing plants but enhanced in the myb15 mutant. At the same time, MYB15 can interact with another key CBF regulator, ICE1, to modulate the expression of CBF genes, indicating the multiple roles of MYB15 in controlling the expression of CBFs during cold stress [67]. The activity and stability of MYB15 are precisely controlled by posttranslational modifications. MPK6 interacts and phosphorylates MYB15 at Ser-168. MPK6-induced phosphorylation reduced the affinity of MYB15 binding to the CBF3 promoter. Compared with MYB15-overexpressing plants, overexpression of MYB15 S168A caused reduced CBF transcript levels in response to cold stress and enhanced sensitivity to freezing [68]. Cold induces the U-box type E3 ubiquitin protein PUB25-and PUB26-mediated degradation of MYB15 to transport cold signaling. PUB25 and PUB26 interact with MYB15 and mediate the ubiquitination of MYB15. The freezing sensitivity in the pub25 pub26 double mutants can largely be rescued by the MYB15 mutation [69].
MYB96 is also induced by cold stress and subsequently activates freezing tolerance through the regulation of CBF expression. Cold induction of CBF and COR genes is diminished in the myb96 mutant. MYB96 regulates the expression of CBFs through HHP proteins. MYB96 positively regulates the expression of HHP1, HHP2, and HHP3 by directly binding to their promoters. HHP1 proteins in turn positively regulate the transcriptional activity of ICE1 through protein-protein interactions and thereby activate downstream CBF expression. The enhanced cold tolerance of the myb96 mutant can be repressed by the mutation of HHP genes, suggesting that MYB96 acts as an upstream regulator of the cold response [70]. Additionally, MYB96 also participates in the cold response through the regulation of LTP3. Overexpression of LTP3 enhanced plant cold tolerance and recovered the hypersensitivity of the myb96 mutant to cold stress [41].
High-temperature stress can also cause damage to the physiological metabolism and growth of plants. MYB30 participates in oxidative and heat stress responses through the regulation of calcium signaling. Plants lacking MYB30 protein exhibit enhanced elevation of [Ca 2+ ] cyt (free Ca 2+ ) in response to H 2 O 2 and heat stimuli. myb30 null mutants exhibited more sensitivity to oxidative stress but resistance to heat shock treatment. The MV and heat sensitivity of myb30 can be suppressed by the application of LaCl 3 , a calcium channel blocker that blocks [Ca 2+ ] cyt elevation. MYB30 regulates calcium signaling by repressing the ANN (ANNEXIN) genes, which encode membrane Ca 2+ transporter proteins modulating cytosolic calcium signatures. MYB30 can directly bind to the promoters of ANN1 and ANN4 to repress their expression. ANN mutations not only blocked abnormal [Ca 2+ ] cyt in the myb30 mutant induced by H 2 O 2 and heat treatment but also suppressed the MV and heat sensitivity of the myb30 mutant [71].

Posttranslational Modifications
The transcriptional activity and protein stability of MYB proteins are precisely regulated by multiple posttranslational modifications. MPK-mediated phosphorylation seems to be one of the major regulators of the activity and stability of MYB proteins. Besides MYB15, MPK6 phosphorylated MYB41 at Ser-251 and enhanced its DNA binding to the promoter of an LTP gene. Overexpression of MYB41 wild-type protein, but not the mutated protein, can enhance plant salt tolerance [72]. MPK4 participates in light-induced anthocyanin accumulation through the regulation of MYB75. MPK4 interacts with MYB75 and mediates the phosphorylation of MYB75. Phosphorylation of MYB75 can increase its stability. Thus, MPK4 promotes anthocyanin biosynthesis through the maintenance of MYB75 stability [73]. In addition to MPK4, MPK3, MPK6, and MPK11 can also interact with MYB75 and mediate its phosphorylation, suggesting the important role of the MPK-MYB75 signaling cascade in anthocyanin biosynthesis [74].
The ubiquitin/26S proteasome pathway is responsible for selective protein turnover. Ubiquitin E3 ligases catalyze the covalent addition of ubiquitin to the target protein and define substrate specificity [75]. Many RING-type E3 ligases have been found to mediate the degradation of MYB proteins. The RING-type ubiquitin E3 ligase COP1 (constitutively photomorphogenic1) mediates light-induced anthocyanin biosynthesis by regulating the stability of MYB75 and MYB90/PAP2. COP1 can interact with MYB75 and MYB90. MYB75 and MYB90 proteins are degraded in the dark, and degradation is dependent on COP1 [76].
The RING-type E3 ubiquitin ligase MIEL1 (MYB30-interacting E3 ligase 1) participates in the HR response by regulating the stability of MYB30. MIEL1 interacts with and ubiquitinates MYB30, leading to MYB30 proteasomal degradation and downregulation of its transcriptional activity. Mutation of MYB30 can restore the hypersensitive phenotype of the miel1 mutant to the HR response [77]. MIEL1 is also involved in ABA regulation of seed germination by promoting MYB96 turnover. MIEL1 can interact with MYB96 and stimulate its ubiquitination and degradation. In contrast to MYB96, the MIEL1-deficient mutant displayed hypersensitivity to ABA during seed germination, whereas MIEL1overexpressing plants were less sensitive. The seed germination rate of the miel1 myb96 double mutant is similar to that of myb96 under ABA treatment, suggesting that MYB96 is epistatic to MIEL1 in the control of seed germination [78].
The degradation of MYB30 in ABA signaling is modulated by the RING-H2 E3 ligase RHA2b. RHA2b interacts with MYB30 to ubiquitinate MYB30, mainly at the Lys-283 site. RHA2b positively regulates the ABA response, as the rha2b mutant is hypersensitive to ABA during seed germination. The stability of MYB30 is significantly improved in the rha2b mutant. MYB30 mutation can block the hyposensitive phenotype of the rha2b mutant to ABA, suggesting that RHA2b participates in seed germination by controlling the stability of MYB30 [79]. In contrast, the stability of MYB30 is maintained by the modification of SUMOylation. The mechanism of SUMOylation is similar to the mechanism of ubiquitination. SUMOE3 ligases catalyze the covalent addition of small ubiquitin-like modifier (SUMO) proteins to the target protein. The SUMO E3 ligase SIZ1 participates in ABA signaling by protecting MYB30 from degradation through SUMOylation. SIZ1mediated SUMOylation plays critical roles in maintaining the stability and transcriptional function of MBY30. Additionally, the SUMOylation site is also localized at the Lys-283 site, suggesting that SUMOylation can protect MYB30 from ubiquitin-mediated proteasomal degradation by occupying the same modification site [58,79]. While SUMO proteases mediate the reversible process of SUMOylation, the deconjugation of SUMO forms the target proteins. ASP1 (SUMO protease 1) positively regulates ABA signaling during early seed development through the regulation of MYB30. In the asp1 mutant, the stability of MBY30 is enhanced, and ABA can induce the expression of ASP1 to modulate the stability of MYB30 [80].

Conclusions and Outlook
Multiple studies have shown that MYB proteins not only participate in the biosynthesis of metabolites such as flavonoids and cuticles, but also play critical roles in the response to abiotic stresses, including drought and cold stresses (Table 1). However, how these MYB proteins are regulated during these processes is still not very clear. Although the expression of MYB genes can be induced by various signals, little is known about the underlying mechanism. For example, MYB4 can inhibit the expression of its own genes, and RdDM-mediated DNA methylation regulates the expression of MYB74. Another question is how to regulate the activity and stability of MYB proteins at the posttranslational level. Phosphorylation and ubiquitination have been shown to play important roles. MPK kinases seem to serve as the major kinases that mediate the phosphorylation of MYB proteins. MPK6 participates in anthocyanin biosynthesis and salt and cold tolerance through the phosphorylation of MYB75, MYB41, and MYB15, respectively. Ubiquitination and SUMOylation antagonistically regulate the stability of the MYB30 protein to modulate ABA signaling in the seed germination process. These findings provide clues for understanding how MYB proteins are regulated at the protein level. Additionally, the MBW transcription factor complex plays important roles in flavonoid pigment biosynthesis, indicating that MYB proteins can function together with other transcription factors. For example, BES1, a key transcription factor in BR signaling, can interact with MYB30, thus activating the expression of BR-responsive genes together with MYB30 [81]. At the same time, MYB30 can interact with MYB96. Although they are both involved in ABA signaling, MYB30 and MYB96 have opposite functions in ABA-mediated seed germination inhibition, suggesting a complicated mechanism for the coregulation of transcription factors. Nevertheless, the function of MYB proteins is in need of much more investigation in the future.