Calcium specificity signaling mechanisms in abscisic acid signal transduction in Arabidopsis guard cells

被引:190
作者
Brandt, Benjamin [1 ]
Munemasa, Shintaro [1 ]
Wang, Cun [1 ]
Desiree Nguyen [1 ]
Yong, Taiming [1 ]
Yang, Paul G. [1 ]
Poretsky, Elly [1 ]
Belknap, Thomas F. [1 ]
Waadt, Rainer [1 ]
Aleman, Fernando [1 ]
Schroeder, Julian I. [1 ]
机构
[1] Univ Calif San Diego, Div Biol Sci, Cell & Dev Biol Sect, San Diego, CA 92103 USA
来源
ELIFE | 2015年 / 4卷
基金
日本学术振兴会; 美国国家科学基金会; 美国国家卫生研究院;
关键词
S-TYPE ANION; ACTIVATED PROTEIN-KINASES; STOMATA; OST1; PLASMA-MEMBRANE; CA2+ CHANNELS; VICIA-FABA; METHYL JASMONATE; GENE-EXPRESSION; USER FUSION; ION-CHANNEL;
D O I
10.7554/eLife.03599
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
A central question is how specificity in cellular responses to the eukaryotic second messenger Ca2+ is achieved. Plant guard cells, that form stomatal pores for gas exchange, provide a powerful system for in depth investigation of Ca2+-signaling specificity in plants. In intact guard cells, abscisic acid (ABA) enhances (primes) the Ca2+-sensitivity of downstream signaling events that result in activation of S-type anion channels during stomatal closure, providing a specificity mechanism in Ca2+-signaling. However, the underlying genetic and biochemical mechanisms remain unknown. Here we show impairment of ABA signal transduction in stomata of calcium-dependent protein kinase quadruple mutant plants. Interestingly, protein phosphatase 2Cs prevent non-specific Ca2+-signaling. Moreover, we demonstrate an unexpected interdependence of the Ca2+-dependent and Ca2+-independent ABA-signaling branches and the in planta requirement of simultaneous phosphorylation at two key phosphorylation sites in SLAC1. We identify novel mechanisms ensuring specificity and robustness within stomatal Ca2+-signaling on a cellular, genetic, and biochemical level.
引用
收藏
页码:1 / 25
页数:25
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