TheArabidopsisphosphatase PP2C49 negatively regulates salt tolerance through inhibition of AtHKT1;1

被引:34
作者
Chu, Moli [1 ]
Chen, Pengwang [1 ]
Meng, Sufang [1 ]
Xu, Peng [1 ]
Lan, Wenzhi [1 ]
机构
[1] Nanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210023, Peoples R China
基金
国家教育部博士点专项基金资助;
关键词
Arabidopsis; AtHKT1; 1; Na plus distribution; translocation; PP2C; salt stress; PROTEIN PHOSPHATASE 2C; ABSCISIC-ACID; SIGNAL-TRANSDUCTION; NA+ TRANSPORT; ANION CHANNEL; STRESS TOLERANCE; PLANT-GROWTH; ARABIDOPSIS; KINASE; SLAC1;
D O I
10.1111/jipb.13008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Type 2C protein phosphatases (PP2Cs) are the largest protein phosphatase family. PP2Cs dephosphorylate substrates for signaling inArabidopsis, but the functions of most PP2Cs remain unknown. Here, we characterized PP2C49 (AT3G62260, a Group G PP2C), which regulates Na(+)distribution under salt stress and is localized to the cytoplasm and nucleus.PP2C49was highly expressed in root vascular tissues and its disruption enhanced plant tolerance to salt stress. Compared with wild type, thepp2c49mutant contained more Na(+)in roots but less Na(+)in shoots and xylem sap, suggesting that PP2C49 regulates shoot Na(+)extrusion. Reciprocal grafting revealed a root-based mechanism underlying the salt tolerance ofpp2c49. Systemic Na(+)distribution largely depends on AtHKT1;1 and loss of function ofAtHKT1;1in thepp2c49background overrode the salt tolerance ofpp2c49, resulting in salt sensitivity. Furthermore, compared with plants overexpressingPP2C49in the wild-type background, plants overexpressingPP2C49in theathtk1;1mutant background were sensitive to salt, like theathtk1;1mutants. Moreover, protein-protein interaction and two-voltage clamping assays demonstrated that PP2C49 physically interacts with AtHKT1;1 and inhibits the Na(+)permeability of AtHKT1;1. This study reveals that PP2C49 negatively regulates AtHKT1;1 activity and thus determines systemic Na(+)allocation during salt stress.
引用
收藏
页码:528 / 542
页数:15
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