The MdWRKY31 transcription factor binds to the MdRAV1 promoter to mediate ABA sensitivity

Xian-Yan Zhao , Chen-Hui Qi , Han Jiang , Chun-Xiang You , Qing-Mei Guan , Feng-Wang Ma , Yuan-Yuan Li , Yu-Jin Hao

Horticulture Research ›› 2019, Vol. 6 ›› Issue (1) : 66

PDF (3363KB)
Horticulture Research ›› 2019, Vol. 6 ›› Issue (1) :66 DOI: 10.1038/s41438-019-0147-1
Article
research-article
The MdWRKY31 transcription factor binds to the MdRAV1 promoter to mediate ABA sensitivity
Author information +
History +
PDF (3363KB)

Abstract

The phytohormone abscisic acid (ABA) is a major element involved in apple (Malus domestica) production because of its role in seed germination and early seedling development. The WRKY family, which is one of the largest families of transcription factors, plays an important role in ABA signaling in plants. However, the underlying molecular mechanisms of WRKY-mediated ABA sensitivity in apple are poorly understood. A genome-wide transcriptome analysis indicated that MdWRKY31 is a key factor induced by ABA. Quantitative real-time PCR showed that MdWRKY31 is induced by ABA in response to PEG4000, which is used to simulate drought. As a transcription factor, MdWRKY31 is localized in the nucleus. Ectopic expression of MdWRKY31 in Arabidopsis and Nicotiana benthamiana enhanced plant sensitivity to ABA. Overexpression of MdWRKY31 in apple roots and apple calli increased sensitivity to ABA, whereas repression of MdWRKY31 reduced sensitivity to ABA in the roots of ‘Royal Gala’. Electrophoretic mobility shift assays, chromatin immunoprecipitation PCR, and yeast one-hybrid assays indicated that MdWRKY31 directly binds to the promoter of MdRAV1. Expression analyses of transgenic apple calli containing MdWRKY31 and pMdRAV1::GUS implied that MdWRKY31 represses the expression of MdRAV1. We also found that MdRAV1 binds directly to the promoters of MdABI3 and MdABI4 and repressed their expression. Our findings reveal a new important regulatory mechanism of MdWRKY31-MdRAV1-MdABIs in the ABA signaling pathway in apple.

Cite this article

Download citation ▾
Xian-Yan Zhao, Chen-Hui Qi, Han Jiang, Chun-Xiang You, Qing-Mei Guan, Feng-Wang Ma, Yuan-Yuan Li, Yu-Jin Hao. The MdWRKY31 transcription factor binds to the MdRAV1 promoter to mediate ABA sensitivity. Horticulture Research, 2019, 6 (1) : 66 DOI:10.1038/s41438-019-0147-1

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Cutler, S. R., Rodriguez, P. L., Finkelstein, R. R. & Abrams, S. R. Abscisic acid: emergence of a core signaling network. Annu. Rev. Plant Biol. 61, 651-679 (2010).

[2]

Raghavendra, A. S., Gonugunta, V. K., Christmann, A. & Grill, E. ABA perception and signalling. Trends Plant Sci. 15, 395-401 (2010).

[3]

Weiner, J. J., Peterson, F. C., Volkman, B. F. & Cutler, S. R. Structural and functional insights into core ABA signaling. Curr. Opin. Plant Biol. 13, 495-502 (2010).

[4]

Wang, S. et al. Abscisic acid is involved in aromatic ester biosynthesis related with ethylene in green apples. J. Plant Physiol. 221, 85-93 (2018).

[5]

Pan, Q. H. et al. Abscisic acid activates acid invertases in developing grape berry. Physiol. Plant. 125, 157-170 (2005).

[6]

Assmann, S. M. Ins and outs of guard cell ABA receptors. Plant Cell 6, 1187-1190 (1994).

[7]

Finkelstein, R. R. & Lynch, T. J. The Arabidopsis abscisic acid response gene ABI5 encodes a basic leucine zipper transcription factor. Plant Cell 12, 599-609 (2000).

[8]

Verslues, P. E. & Zhu, J. K. New developments in abscisic acid perception and metabolism. Curr. Opin. Plant Biol. 10, 447-452 (2007).

[9]

Liu, X. et al. AG protein coupled receptor is a plasma membrane receptor for the plant hormone abscisic acid. Science 315, 1712-1716 (2007).

[10]

Johnston, C. A. et al. Comment on a G protein coupled receptor is a plasma membrane receptor for the plant hormone abscisic acid. Science 318, 914- 914 (2007).

[11]

Pandey, S., Nelson, D. C. & Assmann, S. M. Two novel GPCR-type G proteins are abscisic acid receptors in Arabidopsis. Cell 136, 136-148 (2009).

[12]

Ma, Y. et al. Regulators of PP2C phosphatase activity function as abscisic acid sensors. Science 324, 1064-1068 (2009).

[13]

Park, S. Y. et al. Abscisic acid inhibits type 2C protein phosphatases via the PYR/PYL family of START proteins. Science 324, 1068-1071 (2009).

[14]

Fujii, H. et al. In vitro reconstitution of an abscisic acid signalling pathway. Nature 462, 660-664 (2009).

[15]

Eulgem, T., Rushton, P. J., Robatzek, S. & Somssich, I. E. The WRKY superfamily of plant transcription factors. Trends Plant Sci. 5, 199-206 (2000).

[16]

Rushton, P. J., Somssich, I. E., Ringler, P. & Shen, Q. J. WRKY transcription factors. Trends Plant Sci. 15, 247-258 (2010).

[17]

Finkelstein, R. R., Wang, M. L., Lynch, T. J., Rao, S. & Goodman, H. M. The Arabidopsis abscisic acid response locus ABI4 encodes an APETALA2 domain protein. Plant Cell 10, 1043-1054 (1998).

[18]

Lopez-Molina, L. & Chua, N. H. A null mutation in a bZIP factor confers ABA-insensitivity in Arabidopsis thaliana. Plant Cell Physiol. 41, 541-547 (2000).

[19]

Shang, Y. et al. The Mg-chelatase H subunit of Arabidopsis antagonizes a group of WRKY transcription repressors to relieve ABA-responsive genes of inhibition. Plant Cell 22, 1909-1935 (2010).

[20]

Ren, X. Z. et al. ABO3, a WRKY transcription factor, mediates plant responses to abscisic acid and drought tolerance in Arabidopsis. Plant J. 63, 417-429 (2010).

[21]

Jiang, W. & Yu, D. Arabidopsis WRKY2 transcription factor mediates seed germination and postgermination arrest of development by abscisic acid. BMC Plant Biol. 9, 1471-2229 (2009).

[22]

Ding, Z. J. et al. WRKY 41 controls Arabidopsis seed dormancy via direct regulation of ABI3 transcript levels not downstream of ABA. Plant J. 79, 810-823 (2014).

[23]

Chen, L., Zhang, L., Li, D., Wang, F. & Yu, D. WRKY8 transcription factor functions in the TMV-cg defense response by mediating both abscisic acid and ethylene signaling in Arabidopsis. Proc. Natl Acad. Sci. USA 110, E1963-E1971 (2013).

[24]

Huang, Y., Feng, C. Z., Ye, Q., Wu, W. H. & Chen, Y. F. Arabidopsis WRKY6 transcription factor acts as a positive regulator of abscisic acid signaling during seed germination and early seedling development. PLoS Genet. 12, e1005833 (2016).

[25]

Hu, Y. X., Wang, Y. H., Liu, X. F. & Li, J. Y. Arabidopsis RAV1 is down-regulated by brassinosteroid and may act as a negative regulator during plant development. Cell Res. 14, 8-15 (2004).

[26]

Woo, H. R. et al. The RAV1 transcription factor positively regulates leaf senescence in Arabidopsis. J. Exp. Bot. 61, 3947-3957 (2010).

[27]

Feng, C. Z. et al. Arabidopsis RAV1 transcription factor, phosphorylated by SnRK2 kinases, regulates the expression of ABI3, ABI4, and ABI5 during seed germination and early seedling development. Plant J. 80, 654-668 (2014).

[28]

Chen, H. et al. Roles of Arabidopsis WRKY18, WRKY40 and WRKY60 transcription factors in plant responses to abscisic acid and abiotic stress. BMC Plant Boil. 10, 281 (2010).

[29]

Lee, S. C. & Luan, S. ABA signal transduction at the crossroad of biotic and abiotic stress responses. Plant Cell Environ. 35, 53-60 (2012).

[30]

Wei, W. et al. Ectopic expression of FvWRKY42, a WRKY transcription factor from the diploid woodland strawberry (Fragaria vesca), enhances resistance to powdery mildew, improves osmotic stress resistance, and increases abscisic acid sensitivity in Arabidopsis. Plant Sci. 275, 60-74 (2018).

[31]

Morozova, O., Hirst, M. & Marra, M. A. Applications of new sequencing technologies for transcriptome analysis. Annu. Rev. Genom. Hum. Genet. 10, 135-151 (2009).

[32]

Mutz, K. O., Heilkenbrinker, A., Lönne, M., Walter, J. G. & Stahl, F. Transcriptome analysis using next-generation sequencing. Curr. Opin. Biotechnol. 24, 22-30 (2013).

[33]

Sudhagar, A., Kumar, G. & El-Matbouli, M. Transcriptome analysis based on RNA-seq in understanding pathogenic mechanisms of diseases and the immune system of fish: a comprehensive review. Int. J. Mol. Sci. 19, 245 (2018).

[34]

Dong, H. et al. Transcriptome analysis of soybean WRKY TFs in response to Peronospora manshurica infection. Genomics.(2018). https://doi.org/10.1016/j.ygeno.2018.09.014.

[35]

Cheng, H. & Wang, S. The important player of rice-pathogen interactions: WRKY-type transcription factors. Sci. Sin. Vitae 44, 784-793 (2014).

[36]

Liu, Q. et al. OsWRKY67 positively regulates blast and bacteria blight resistance by direct activation of PR genes in rice. BMC Plant Biol. 18, 257 (2018).

[37]

Zhang, L. L. et al. Overexpression of VaWRKY14 increases drought tolerance in Arabidopsis by modulating the expression of stress-related genes. Plant Cell Rep. 37, 1159-1172 (2018).

[38]

Zhang, Y. et al. CsWRKY46, a WRKY transcription factor from cucumber, confers cold resistance in transgenic-plant by regulating a set of cold-stress responsive genes in an ABA-dependent manner. Plant Physiol. Biochem. 108, 478-487 (2016).

[39]

Ullah, A., Sun, H., Yang, X. & Zhang, X. A novel cotton WRKY gene, GhWRKY6-like, improves salt tolerance by activating the ABA signaling pathway and scavenging of reactive oxygen species. Physiol. Plant. 162, 439-454 (2018).

[40]

Ma, Q. J. et al. An apple CIPK protein kinase targets a novel residue of AREB transcription factor for ABA-dependent phosphorylation. Plant Cell Environ. 40, 2207-2219 (2017).

[41]

Kang, J. Y., Choi, H. I., Im, M. Y. & Kim, S. Y. Arabidopsis basic leucine zipper proteins that mediate stress-responsive abscisic acid signaling. Plant Cell 14, 343-357 (2002).

[42]

Kim, S., Kang, J. Y., Cho, D. I., Park, J. H. & Kim, S. Y. ABF2, an ABRE-binding bZIP factor, is an essential component of glucose signaling and its overexpression affects multiple stress tolerance. Plant J. 40, 75-87 (2004).

[43]

Apel, K. & Hirt, H. Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annu. Rev. Plant Biol. 55, 373-399 (2004).

[44]

Pei, Z. M. et al. Calcium channels activated by hydrogen peroxide mediate abscisic acid signalling in guard cells. Nature 406, 731 (2000).

[45]

Delledonne, M., Zeier, J., Marocco, A. & Lamb, C. Signal interactions between nitric oxide and reactive oxygen intermediates in the plant hypersensitive disease resistance response. Proc. Natl Acad. Sci. USA 98, 13454-13459 (2001).

[46]

Asada, K. Production and scavenging of reactive oxygen species in chloroplasts and their functions. Plant Physiol. 141, 391-396 (2006).

[47]

Parcy, F. et al. Regulation of gene expression programs during Arabidopsis seed development: roles of the ABI3 locus and of endogenous abscisic acid. Plant Cell 6, 1567-1582 (1994).

[48]

Lopez‐Molina, L., Mongrand, S., McLachlin, D. T., Chait, B. T. & Chua, N. H. ABI5 acts downstream of ABI3 to execute an ABA‐dependent growth arrest during germination. Plant J. 32, 317-328 (2002).

[49]

Shu, K. et al. ABI4 regulates primary seed dormancy by regulating the biogenesis of abscisic acid and gibberellins in. Arab.. PLoS Genet. 9, e1003577 (2013).

[50]

Shu, K. et al. ABI4 regulates the floral transition independently of ABI5 and ABI3. Mol. Biol. Rep. 45, 2727-2731 (2018).

[51]

Zhang, X., Garreton, V. & Chua, N. H. The AIP2 E3 ligase acts as a novel negative regulator of ABA signaling by promoting ABI3 degradation. Genes Dev. 19, 1532-1543 (2005).

[52]

Bossi, F. et al. The Arabidopsis ABA‐INSENSITIVE (ABI) 4 factor acts as a central transcription activator of the expression of its own gene, and for the induction of ABI5 and SBE2. 2 genes during sugar signaling. Plant J. 59, 359-374 (2009).

[53]

Lopez-Molina, L., Mongrand, S., Kinoshita, N. & Chua, N. H. AFP is a novel negative regulator of ABA signaling that promotes ABI5 protein degradation. Genes Dev. 17, 410-418 (2003).

[54]

Gao, S. et al. ABF2, ABF3, and ABF4 promote ABA-mediated chlorophyll degradation and leaf senescence by transcriptional activation of chlorophyll catabolic genes and senescence-associated genes in Arabidopsis. Mol. Plant 9, 1272-1285 (2016).

[55]

Nishimura, N. et al. Structural mechanism of abscisic acid binding and signaling by dimeric PYR1. Science 326, 1373-1379 (2009).

[56]

Santiago, J. et al. The abscisic acid receptor PYR1 in complex with abscisic acid. Nature 462, 665-668 (2009).

[57]

Su, T. et al. WRKY42 modulates phosphate homeostasis through regulating phosphate translocation and acquisition in Arabidopsis. Plant Physiol. 4, 1579-1591 (2015).

[58]

An, J. P. et al. Ectopic expression of an apple cytochrome P450 gene MdCYPM1 negatively regulates plant photomorphogenesis and stress response in Arabidopsis. Biochem. Bioph. Res. Co. 483, 1-9 (2017).

[59]

Zhao, Q. et al. Overexpression of MdbHLH104 gene enhances the tolerance to iron deficiency in apple. Plant Biotechnol. J. 14, 1633-1645 (2016).

[60]

Hu, D. G. et al. MdMYB1 regulates anthocyanin and malate accumulation by directly facilitating their transport into vacuoles in apples. Plant Physiol. 170, 1315-1330 (2016).

[61]

Xie, X. B. et al. The bHLH transcription factor MdbHLH3 promotes anthocyanin accumulation and fruit colouration in response to low temperature in apples. Plant Cell Environ. 35, 1884-1897 (2012).

PDF (3363KB)

0

Accesses

0

Citation

Detail

Sections
Recommended

/