染色质
表观基因组
生物
脱甲基酶
DNA修复
染色质重塑
细胞生物学
PARP1
DNA损伤
组蛋白
表观遗传学
遗传学
DNA
基因
DNA甲基化
聚ADP核糖聚合酶
基因表达
聚合酶
作者
Anthony Sanchez,Bethany A. Buck‐Koehntop,Kyle M. Miller
出处
期刊:BioEssays
[Wiley]
日期:2022-05-09
卷期号:44 (7)
被引量:3
标识
DOI:10.1002/bies.202200015
摘要
The lysine demethylase KDM5A collaborates with PARP1 and the histone variant macroH2A1.2 to modulate chromatin to promote DNA repair. Indeed, KDM5A engages poly(ADP-ribose) (PAR) chains at damage sites through a previously uncharacterized coiled-coil domain, a novel binding mode for PAR interactions. While KDM5A is a well-known transcriptional regulator, its function in DNA repair is only now emerging. Here we review the molecular mechanisms that regulate this PARP1-macroH2A1.2-KDM5A axis in DNA damage and consider the potential involvement of this pathway in transcription regulation and cancer. Using KDM5A as an example, we discuss how multifunctional chromatin proteins transition between several DNA-based processes, which must be coordinated to protect the integrity of the genome and epigenome. The dysregulation of chromatin and loss of genome integrity that is prevalent in human diseases including cancer may be related and could provide opportunities to target multitasking proteins with these pathways as therapeutic strategies.
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