Chu Moli, Chen Pengwang, Meng Sufang, Xu Peng, Lan Wenzhi
State Key Laboratory for Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, 210023, China.
J Integr Plant Biol. 2021 Mar;63(3):528-542. doi: 10.1111/jipb.13008. Epub 2020 Oct 10.
Type 2C protein phosphatases (PP2Cs) are the largest protein phosphatase family. PP2Cs dephosphorylate substrates for signaling in Arabidopsis, 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. PP2C49 was highly expressed in root vascular tissues and its disruption enhanced plant tolerance to salt stress. Compared with wild type, the pp2c49 mutant 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 of pp2c49. Systemic Na distribution largely depends on AtHKT1;1 and loss of function of AtHKT1;1 in the pp2c49 background overrode the salt tolerance of pp2c49, resulting in salt sensitivity. Furthermore, compared with plants overexpressing PP2C49 in the wild-type background, plants overexpressing PP2C49 in the athtk1;1 mutant background were sensitive to salt, like the athtk1;1 mutants. 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.
2C型蛋白磷酸酶(PP2Cs)是最大的蛋白磷酸酶家族。PP2Cs使拟南芥中用于信号传导的底物去磷酸化,但大多数PP2Cs的功能仍不清楚。在这里,我们对PP2C49(AT3G62260,G组PP2C)进行了表征,它在盐胁迫下调节钠的分布,定位于细胞质和细胞核。PP2C49在根维管组织中高度表达,其缺失增强了植物对盐胁迫的耐受性。与野生型相比,pp2c49突变体根部的钠含量更多,但地上部和木质部汁液中的钠含量更少,这表明PP2C49调节地上部钠的外排。相互嫁接揭示了pp2c49耐盐性的基于根的机制。系统性钠分布很大程度上取决于AtHKT1;1,在pp2c49背景下AtHKT1;1功能丧失抵消了pp2c49的耐盐性,导致盐敏感。此外,与在野生型背景中过表达PP2C49的植物相比,在athkt1;1突变体背景中过表达PP2C49的植物对盐敏感,就像athkt1;1突变体一样。此外,蛋白质-蛋白质相互作用和双电压钳试验表明,PP2C49与AtHKT1;1发生物理相互作用并抑制AtHKT1;1的钠通透性。这项研究表明,PP2C49负向调节AtHKT1;1的活性,从而决定盐胁迫期间系统性钠的分配。