EGR1 and EGR2 positively regulate plant ABA signaling by modulating the phosphorylation of SnRK2.2

磷酸化 生物 细胞生物学 化学 信号转导
作者
Chuanling Li,Xuetong Li,Zhiping Deng,Yuning Song,Xinye Liu,Xiaohan Alex Tang,Ziye Li,Ya Zhang,Baowen Zhang,Wenqiang Tang,Jian‐Xiu Shang,Yu Sun
出处
期刊:New Phytologist [Wiley]
卷期号:241 (4): 1492-1509 被引量:3
标识
DOI:10.1111/nph.19458
摘要

Summary During abscisic acid (ABA) signaling, reversible phosphorylation controls the activity and accumulation of class III SNF1‐RELATED PROTEIN KINASE 2s (SnRK2s). While protein phosphatases that negatively regulate SnRK2s have been identified, those that positively regulate ABA signaling through SnRK2s are less understood. In this study, Arabidopsis thaliana mutants of Clade E Growth‐Regulating 1 and 2 (EGR1/2), which belong to the protein phosphatase 2C family, exhibited reduced ABA sensitivity in terms of seed germination, cotyledon greening, and ABI5 accumulation. Conversely, overexpression increased these ABA‐induced responses. Transcriptomic data revealed that most ABA‐regulated genes in egr1 egr2 plants were expressed at reduced levels compared with those in Col‐0 after ABA treatment. Abscisic acid up‐regulated EGR1/2, which interact directly with SnRK2.2 through its C‐terminal domain I. Genetic analysis demonstrated that EGR1/2 function through SnRK2.2 during ABA response. Furthermore, SnRK2.2 de‐phosphorylation by EGR1/2 was identified at serine 31 within the ATP‐binding pocket. A phospho‐mimic mutation confirmed that phosphorylation at serine 31 inhibited SnRK2.2 activity and reduced ABA responsiveness in plants. Our findings highlight the positive role of EGR1/2 in regulating ABA signaling, they reveal a new mechanism for modulating SnRK2.2 activity, and provide novel insight into how plants fine‐tune their responses to ABA.
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