组蛋白
染色质
生物
组蛋白密码
表观遗传学
DNA损伤
表观遗传学
细胞生物学
组蛋白修饰酶
组蛋白H2A
癌症表观遗传学
DNA修复
染色质重塑
遗传学
组蛋白甲基化
组蛋白甲基转移酶
DNA甲基化
DNA
核小体
基因
基因表达
作者
Jae Jin Kim,Seo Yun Lee,Kyle M. Miller
标识
DOI:10.1080/10409238.2019.1620676
摘要
Modulation of chromatin templates in response to cellular cues, including DNA damage, relies heavily on the post-translation modification of histones. Numerous types of histone modifications including phosphorylation, methylation, acetylation, and ubiquitylation occur on specific histone residues in response to DNA damage. These histone marks regulate both the structure and function of chromatin, allowing for the transition between chromatin states that function in undamaged condition to those that occur in the presence of DNA damage. Histone modifications play well-recognized roles in sensing, processing, and repairing damaged DNA to ensure the integrity of genetic information and cellular homeostasis. This review highlights our current understanding of histone modifications as they relate to DNA damage responses (DDRs) and their involvement in genome maintenance, including the potential targeting of histone modification regulators in cancer, a disease that exhibits both epigenetic dysregulation and intrinsic DNA damage.
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