Role of H3K9 demethylases in DNA double-strand break repair.

Hee-Young Jeon, Arif Hussain, Jianfei Qi
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引用次数: 6

Abstract

H3K9 demethylases can remove the repressive H3K9 methylation marks on histones to alter chromatin structure, gene transcription and epigenetic state of cells. By counteracting the function of H3K9 methyltransferases, H3K9 demethylases have been shown to play an important role in numerous biological processes, including diseases such as cancer. Recent evidence points to a key role for some H3K9 demethylases in the repair of DNA double-strand breaks (DSBs) via homologous recombination (HR) and/or non-homologous end joining (NHEJ) pathways. Mechanistically, H3K9 demethylases can upregulate the expression of DNA repair factors. They can also be recruited to the DNA damage sites and regulate the recruitment or function of DNA repair factors. Here, we will discuss the role and mechanisms of H3K9 demethylases in the regulation of DSB repair.

H3K9去甲基酶在DNA双链断裂修复中的作用。
H3K9去甲基化酶可以去除组蛋白上的抑制H3K9甲基化标记,从而改变细胞的染色质结构、基因转录和表观遗传状态。通过抵消H3K9甲基转移酶的功能,H3K9去甲基化酶已被证明在许多生物过程中发挥重要作用,包括癌症等疾病。最近的证据表明,一些H3K9去甲基化酶通过同源重组(HR)和/或非同源末端连接(NHEJ)途径在DNA双链断裂(DSBs)修复中起关键作用。机制上,H3K9去甲基化酶可以上调DNA修复因子的表达。它们也可以被招募到DNA损伤位点,调节DNA修复因子的招募或功能。在这里,我们将讨论H3K9去甲基化酶在调节DSB修复中的作用和机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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