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酪蛋白激酶1样蛋白2通过肌动蛋白解聚因子的磷酸化调节肌动蛋白丝稳定性和气孔关闭。

CASEIN KINASE1-LIKE PROTEIN2 Regulates Actin Filament Stability and Stomatal Closure via Phosphorylation of Actin Depolymerizing Factor.

作者信息

Zhao Shuangshuang, Jiang Yuxiang, Zhao Yang, Huang Shanjin, Yuan Ming, Zhao Yanxiu, Guo Yan

机构信息

Key Laboratory of Plant Stress, Life Science College, Shandong Normal University, Jinan 250014, China State Key Laboratory of Plant Physiology and Biochemistry, College of Biological Sciences, China Agricultural University, Beijing 100193, China.

Key Laboratory of Plant Molecular Physiology, Institute of Botany, Chinese Academy of Science, Beijing 100093, China.

出版信息

Plant Cell. 2016 Jun;28(6):1422-39. doi: 10.1105/tpc.16.00078. Epub 2016 Jun 7.

Abstract

The opening and closing of stomata are crucial for plant photosynthesis and transpiration. Actin filaments undergo dynamic reorganization during stomatal closure, but the underlying mechanism for this cytoskeletal reorganization remains largely unclear. In this study, we identified and characterized Arabidopsis thaliana casein kinase 1-like protein 2 (CKL2), which responds to abscisic acid (ABA) treatment and participates in ABA- and drought-induced stomatal closure. Although CKL2 does not bind to actin filaments directly and has no effect on actin assembly in vitro, it colocalizes with and stabilizes actin filaments in guard cells. Further investigation revealed that CKL2 physically interacts with and phosphorylates actin depolymerizing factor 4 (ADF4) and inhibits its activity in actin filament disassembly. During ABA-induced stomatal closure, deletion of CKL2 in Arabidopsis alters actin reorganization in stomata and renders stomatal closure less sensitive to ABA, whereas deletion of ADF4 impairs the disassembly of actin filaments and causes stomatal closure to be more sensitive to ABA Deletion of ADF4 in the ckl2 mutant partially recues its ABA-insensitive stomatal closure phenotype. Moreover, Arabidopsis ADFs from subclass I are targets of CKL2 in vitro. Thus, our results suggest that CKL2 regulates actin filament reorganization and stomatal closure mainly through phosphorylation of ADF.

摘要

气孔的开闭对植物光合作用和蒸腾作用至关重要。肌动蛋白丝在气孔关闭过程中会发生动态重组,但其细胞骨架重组的潜在机制仍不清楚。在本研究中,我们鉴定并表征了拟南芥酪蛋白激酶1样蛋白2(CKL2),它对脱落酸(ABA)处理有反应,并参与ABA和干旱诱导的气孔关闭。虽然CKL2不直接与肌动蛋白丝结合,且在体外对肌动蛋白组装没有影响,但它在保卫细胞中与肌动蛋白丝共定位并使其稳定。进一步研究表明,CKL2与肌动蛋白解聚因子4(ADF4)发生物理相互作用并使其磷酸化,从而抑制其在肌动蛋白丝解聚中的活性。在ABA诱导的气孔关闭过程中,拟南芥中CKL2的缺失改变了气孔中的肌动蛋白重组,使气孔关闭对ABA的敏感性降低,而ADF4的缺失则损害了肌动蛋白丝的解聚,导致气孔关闭对ABA更敏感。在ckl2突变体中缺失ADF4可部分恢复其对ABA不敏感的气孔关闭表型。此外,来自I亚类的拟南芥ADF是CKL2在体外的作用靶点。因此,我们的结果表明,CKL2主要通过对ADF的磷酸化来调节肌动蛋白丝重组和气孔关闭。

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