Type 2C protein phosphatase clade D family members dephosphorylate guard cell plasma membrane H+-ATPase

Mitsumasa Akiyama, Hodaka Sugimoto, Shin Ichiro Inoue, Yohei Takahashi, Maki Hayashi, Yuki Hayashi, Miya Mizutani, Takumi Ogawa, Daichi Kinoshita, Eigo Ando, Meeyeon Park, William M. Gray, Toshinori Kinoshita

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Abstract

Plasma membrane (PM) H + -ATPase in guard cells is activated by phosphorylation of the penultimate residue, threonine (Thr), in response to blue and red light, promoting stomatal opening. Previous in vitro biochemical investigation suggested that Mg2 + - and Mn2 + -dependent membrane-localized type 2C protein phosphatase (PP2C)-like activity mediates the dephosphorylation of PM H + -ATPase in guard cells. PP2C clade D (PP2C.D) was later demonstrated to be involved in PM H + -ATPase dephosphorylation during auxin-induced cell expansion in Arabidopsis (Arabidopsis thaliana). However, it is unclear whether PP2C.D phosphatases are involved in PM H + -ATPase dephosphorylation in guard cells. Transient expression experiments using Arabidopsis mesophyll cell protoplasts revealed that all PP2C.D isoforms dephosphorylate the endogenous PM H + -ATPase. We further analyzed PP2C.D6/8/9, which display higher expression levels than other isoforms in guard cells, observing that pp2c.d6, pp2c.d8, and pp2c.d9 single mutants showed similar light-induced stomatal opening and phosphorylation status of PM H + -ATPase in guard cells as Col-0. In contrast, the pp2c.d6/9 double mutant displayed wider stomatal apertures and greater PM H + -ATPase phosphorylation in response to blue light, but delayed dephosphorylation of PM H + -ATPase in guard cells; the pp2c.d6/8/9 triple mutant showed similar phenotypes to those of the pp2c.d6/9 double mutant. Taken together, these results indicate that PP2C.D6 and PP2C.D9 redundantly mediate PM H + -ATPase dephosphorylation in guard cells. Curiously, unlike auxin-induced cell expansion in seedlings, auxin had no effect on the phosphorylation status of PM H + -ATPase in guard cells.

Original languageEnglish (US)
Pages (from-to)2228-2240
Number of pages13
JournalPlant physiology
Volume188
Issue number4
DOIs
StatePublished - Apr 2022

Bibliographical note

Funding Information:
This work was supported by Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science, and Technology, Japan (grant nos. 20H05687 and 20H05910 to T.K.), by Technology of Japan and from the Advanced Low Carbon Technology Research and Development Program from the Japan Science and Technology Agency (JPMJAL1011 to T.K.), the National Science Foundation (MCB-1613809 to W.M.G.), and the National Institutes of Health (GM067203 to W.M.G.).

Publisher Copyright:
© The Author(s) 2021.

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