Phosphorylation of BLUS1 kinase by phototropins is a primary step in stomatal opening

被引:159
作者
Takemiya, Atsushi [1 ]
Sugiyama, Naoyuki [2 ]
Fujimoto, Hiroshi [1 ]
Tsutsumi, Toshifumi [1 ]
Yamauchi, Shota [1 ]
Hiyama, Asami [1 ]
Tada, Yasuomi [3 ]
Christie, John M. [4 ]
Shimazaki, Ken-ichiro [1 ]
机构
[1] Kyushu Univ, Fac Sci, Dept Biol, Fukuoka 8128581, Japan
[2] Keio Univ, Inst Adv Biosci, Tsuruoka, Yamagata 9970017, Japan
[3] Kagawa Univ, Life Sci Res Ctr, Inst Res Promot, Kagawa 7610795, Japan
[4] Univ Glasgow, Coll Med Vet & Life Sci, Inst Mol Cell & Syst Biol, Glasgow G12 8QQ, Lanark, Scotland
关键词
MEMBRANE H+-ATPASE; GUARD-CELL PROTOPLASTS; PROTEIN-KINASE; LIGHT; NANOELECTROSPRAY; CHROMATOGRAPHY; ACTIVATION; RESPONSES; INSIGHTS; PHOT1;
D O I
10.1038/ncomms3094
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Opening of stomata in the plant facilitates photosynthetic CO2 fixation and transpiration. Blue-light perception by phototropins (phot1, phot2) activates the plasma membrane H+-ATPase, causing stomata to open. Here we describe a regulator that connects these components, a Ser/Thr protein kinase, BLUS1 (BLUE LIGHT SIGNALING1), which mediates a primary step for phototropin signalling in guard cells. blus1 mutants identified by infrared thermography result in a loss of blue light-dependent stomatal opening. BLUS1 encodes a protein kinase that is directly phosphorylated by phot1 in vitro and in vivo at Ser-348 within its C-terminus. Both phosphorylation of Ser-348 and BLUS1 kinase activity are essential for activation of the H+-ATPase. blus1 mutants show lower stomatal conductance and CO2 assimilation than wild-type plants under decreased ambient CO2. Together, our analyses demonstrate that BLUS1 functions as a phototropin substrate and primary regulator of stomatal control to enhance photosynthetic CO2 assimilation under natural light conditions.
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页数:8
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