生物
DNA损伤
聚ADP核糖聚合酶
DNA修复
染色质
细胞生物学
基因组不稳定性
DNA复制
DNA
DNA断裂
聚合酶
遗传学
复制蛋白A
分子生物学
程序性细胞死亡
基因
DNA结合蛋白
转录因子
细胞凋亡
作者
Yingfei Wang,Weibo Luo
出处
期刊:DNA Repair
[Elsevier]
日期:2019-09-01
卷期号:81: 102651-102651
被引量:114
标识
DOI:10.1016/j.dnarep.2019.102651
摘要
Poly(ADP-ribose) (PAR) polymerase-1 (PARP-1) acts as a DNA damage sensor. It recognizes DNA damage and facilitates DNA repair by recruiting DNA repair machinery to damage sites. Recent studies reported that PARP-1 also plays an important role in DNA replication by recognizing the unligated Okazaki fragments and controlling the speed of fork elongation. On the other hand, emerging evidence reveals that excessive activation of PARP-1 causes chromatin DNA fragmentation and triggers an intrinsic PARP-1-dependent cell death program designated parthanatos, which can be blocked by genetic deletion or pharmacological inhibition of PARP-1. Therefore, PARP-1 plays an essential role in maintaining genomic stability by either facilitating DNA repair/replication or triggering DNA fragmentation to kill cells. A group of structure-specific nucleases is crucial for executing DNA incision and fragmentation following PARP-1 activation. In this review, we will discuss how PARP-1 coordinates with its associated nucleases to maintain genomic integrity and control the decision of cell life and death.
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