Dynamic Phosphorylation of G9a Regulates its Repressive Activity on Chromatin Accessibility and Mitotic Progression

Author:

Geng Qizhi1,Kong Yue‐Yu1,Li Weizhe1,Zhang Jianhao2,Ma Haoli3,Zhang Yuhang2,Da Lin‐Tai4,Zhao Yan3,Du Hai‐Ning1ORCID

Affiliation:

1. Hubei Key Laboratory of Cell Homeostasis College of Life Sciences Hubei Clinical Research Center of Emergency and Resuscitation Emergency Center of Zhongnan Hospital of Wuhan University Frontier Science Center for Immunology and Metabolism RNA Institute Wuhan University Wuhan 430072 China

2. School of Life Sciences and Biotechnology Shanghai JiaoTong University Shanghai 200240 China

3. Hubei Clinical Research Center of Emergency and Resuscitation Emergency Center of Zhongnan Hospital of Wuhan University Wuhan University Wuhan 430071 China

4. Shanghai Center for Systems Biomedicine Shanghai JiaoTong University Shanghai 200240 China

Abstract

AbstractPhosphorylation of Ser10 of histone H3 (H3S10p), together with the adjacent methylation of Lys9 (H3K9me), has been proposed to function as a ‘phospho‐methyl switch’ to regulate mitotic chromatin architecture. Despite of immense understanding of the roles of H3S10 phosphorylation, how H3K9me2 are dynamically regulated during mitosis is poorly understood. Here, it is identified that Plk1 kinase phosphorylates the H3K9me1/2 methyltransferase G9a/EHMT2 at Thr1045 (pT1045) during early mitosis, which attenuates its catalytic activity toward H3K9me2. Cells bearing Thr1045 phosphomimic mutant of G9a (T1045E) show decreased H3K9me2 levels, increased chromatin accessibility, and delayed mitotic progression. By contrast, dephosphorylation of pT1045 during late mitosis by the protein phosphatase PPP2CB reactivates G9a activity and upregulates H3K9me2 levels, correlated with decreased levels of H3S10p. Therefore, the results provide a mechanistic explanation of the essential of a ‘phospho‐methyl switch’ and highlight the importance of Plk1 and PPP2CB‐mediated dynamic regulation of G9a activity in chromatin organization and mitotic progression.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Wiley

Subject

General Physics and Astronomy,General Engineering,Biochemistry, Genetics and Molecular Biology (miscellaneous),General Materials Science,General Chemical Engineering,Medicine (miscellaneous)

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