The clade F PP2C phosphatase ZmPP84 negatively regulates drought tolerance by repressing stomatal closure in maize

被引:37
作者
Guo, Yazhen [1 ]
Shi, Yabo [1 ]
Wang, Yalin [1 ]
Liu, Fang [1 ,2 ]
Li, Zhen [1 ]
Qi, Junsheng [1 ]
Wang, Yi [1 ]
Zhang, Jingbo [3 ]
Yang, Shuhua [1 ]
Wang, Yu [1 ]
Gong, Zhizhong [1 ,4 ]
机构
[1] China Agr Univ, Coll Biol Sci, State Key Lab Plant Physiol & Biochem, Beijing 100193, Peoples R China
[2] China Agr Univ, Ctr Crop Funct Genom & Mol Breeding, Beijing 100193, Peoples R China
[3] China Agr Univ, Coll Resources & Environm Sci, Beijing 100193, Peoples R China
[4] Hebei Univ, Inst Life Sci & Green Dev, Sch Life Sci, Baoding 071002, Peoples R China
基金
中国国家自然科学基金;
关键词
drought tolerance; maize; protein kinase; protein phosphatase; stomatal movement; ANION CHANNEL SLAC1; ABSCISIC-ACID; PROTEIN-KINASES; POPULATION-GENETICS; LOCAL ADAPTATION; SELECTIVE SWEEPS; RECEPTOR KINASE; OVER-EXPRESSION; MAP KINASES; STRESS;
D O I
10.1111/nph.18647
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Drought is a major environmental stress that threatens crop production. Therefore, identification of genes involved in drought stress response is of vital importance to decipher the molecular mechanism of stress signal transduction and breed drought tolerance crops, especially for maize. Clade A PP2C phosphatases are core abscisic acid (ABA) signaling components, regulating ABA signal transduction and drought response. However, the roles of other clade PP2Cs in drought resistance remain largely unknown. Here, we discovered a clade F PP2C, ZmPP84, that negatively regulates drought tolerance by screening a transgenic overexpression maize library. Quantitative RT-PCR indicates that the transcription of ZmPP84 is suppressed by drought stress. We identified that ZmMEK1, a member of the MAPKK family, interacts with ZmPP84 by immunoprecipitation and mass spectrometry analysis. Additionally, we found that ZmPP84 can dephosphorylate ZmMEK1 and repress its kinase activity on the downstream substrate kinase ZmSIMK1, while ZmSIMK1 is able to phosphorylate S-type anion channel ZmSLAC1 at S146 and T520 in vitro. Mutations of S146 and T520 to phosphomimetic aspartate could activate ZmSLAC1 currents in Xenopus oocytes. Taken together, our study suggests that ZmPP84 is a negative regulator of drought stress response that inhibits stomatal closure through dephosphorylating ZmMEK1, thereby repressing ZmMEK1-ZmSIMK1 signaling pathway.
引用
收藏
页码:1728 / 1744
页数:17
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