生物
G2-M DNA损伤检查点
DNA损伤
细胞生物学
DNA修复
细胞周期检查点
支票1
组蛋白
调节器
小干扰RNA
DNA
细胞周期
分子生物学
遗传学
核糖核酸
细胞
基因
作者
Manuel Stucki,Stephen Jackson
出处
期刊:DNA Repair
[Elsevier BV]
日期:2004-04-10
卷期号:3 (8-9): 953-957
被引量:115
标识
DOI:10.1016/j.dnarep.2004.03.007
摘要
The protein MDC1/NFBD1 contains a forkhead-associated (FHA) domain and two BRCA1 carboxyl-terminal (BRCT) domains. It interacts with several proteins involved in DNA damage repair and checkpoint signalling, and is phosphorylated in response to DNA damage and during mitosis. Upon treatment of cultured human cells with DNA damaging agents, MDC1/NFBD1 translocates to sites of DNA lesions, where it collaborates with other proteins and with phosphorylated histone H2AX to mediate the accumulation of checkpoint and repair factors into nuclear foci. Down-regulation of MDC1/NFBD1 expression levels by small interfering RNA (siRNA) renders cells hyper-sensitive to DNA damaging agents and leads to defects in cell cycle checkpoint activation and apoptosis. Thus, MDC1/NFBD1 appears to be a key regulator of the DNA damage response in mammalian cells.
科研通智能强力驱动
Strongly Powered by AbleSci AI