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

• Published in: The Plant cell Vol. 28; no. 6; pp. 1422 - 1439
• Main Authors: Zhao, Shuangshuang, Jiang, Yuxiang, Zhao, Yang, Huang, Shanjin, Yuan, Ming, Zhao, Yanxiu, Guo, Yan
• Format: Journal Article
• Language: English
• Published: United States American Society of Plant Biologists 01-06-2016
• Subjects: Abscisic Acid - pharmacology; Actin Cytoskeleton - drug effects; Actin Cytoskeleton - metabolism; Actin Depolymerizing Factors - genetics; Actin Depolymerizing Factors - metabolism; Arabidopsis; Arabidopsis - drug effects; Arabidopsis - genetics; Arabidopsis - metabolism; Arabidopsis Proteins - genetics; Arabidopsis Proteins - metabolism; Arabidopsis thaliana; Droughts; Phosphorylation - drug effects; Phosphorylation - genetics; Plant Stomata - drug effects; Plant Stomata - metabolism; Signal Transduction - drug effects; Signal Transduction - genetics
• ISSN: 1040-4651; 1532-298X
• DOI: 10.1105/tpc.16.00078

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.