Xie Qi, Bai Yujie, Wu Junbing, Sun Yu, Wang Yadong, Zhang Ye, Mei Pinchao, Yuan Zengqiang
Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.
J Recept Signal Transduct Res. 2011 Apr;31(2):139-46. doi: 10.3109/10799893.2011.552914. Epub 2011 Feb 15.
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.
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。