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DNA损伤诱导的细胞死亡中E2F1的甲基化介导调控

Methylation-mediated regulation of E2F1 in DNA damage-induced cell death.

作者信息

Xie Qi, Bai Yujie, Wu Junbing, Sun Yu, Wang Yadong, Zhang Ye, Mei Pinchao, Yuan Zengqiang

机构信息

Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.

出版信息

J Recept Signal Transduct Res. 2011 Apr;31(2):139-46. doi: 10.3109/10799893.2011.552914. Epub 2011 Feb 15.

Abstract

E2F1 promotes DNA damage-induced apoptosis and the post-translational modifications of E2F1 play an important role in the regulation of E2F1-mediated cell death. Here, we found that Set9 and LSD1 regulate E2F1-mediated apoptosis upon DNA damage. Set9 methylates E2F1 at lysine 185, a conserved residue in the DNA-binding domain of E2F family proteins. The methylation of E2F1 by Set9 leads to the stabilization of E2F1 and up-regulation of its proapoptotic target genes p73 and Bim, and thereby induces E2F1-mediated apoptosis in response to genotoxic agents. We also found that LSD1 demethylates E2F1 at lysine 185 and reduces E2F1-mediated cell death. The identification of the methylation/demethylation of E2F1 by Set9/LSD1 suggests that E2F1 is dynamically regulated by epigenetic enzymes in response to DNA damage.

摘要

E2F1促进DNA损伤诱导的细胞凋亡,并且E2F1的翻译后修饰在E2F1介导的细胞死亡调控中发挥重要作用。在此,我们发现Set9和LSD1在DNA损伤时调节E2F1介导的细胞凋亡。Set9使E2F1在赖氨酸185处发生甲基化,赖氨酸185是E2F家族蛋白DNA结合结构域中的一个保守残基。Set9介导的E2F1甲基化导致E2F1的稳定及其促凋亡靶基因p73和Bim的上调,从而在响应基因毒性剂时诱导E2F1介导的细胞凋亡。我们还发现LSD1使E2F1在赖氨酸185处去甲基化并减少E2F1介导的细胞死亡。Set9/LSD1对E2F1甲基化/去甲基化的鉴定表明,E2F1在响应DNA损伤时受到表观遗传酶的动态调控。

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