Stucki Manuel, Jackson Stephen P
Department of Zoology, The Wellcome Trust/Cancer Research UK, Gurdon Institute of Cancer and Developmental Biology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QR, UK.
DNA Repair (Amst). 2004 Aug-Sep;3(8-9):953-7. doi: 10.1016/j.dnarep.2004.03.007.
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.
蛋白质MDC1/NFBD1包含一个叉头相关(FHA)结构域和两个BRCA1羧基末端(BRCT)结构域。它与多种参与DNA损伤修复和检查点信号传导的蛋白质相互作用,并在DNA损伤响应和有丝分裂过程中发生磷酸化。在用DNA损伤剂处理培养的人类细胞后,MDC1/NFBD1会转移到DNA损伤位点,在那里它与其他蛋白质以及磷酸化的组蛋白H2AX协同作用,介导检查点和修复因子在核灶中的积累。通过小干扰RNA(siRNA)下调MDC1/NFBD1的表达水平会使细胞对DNA损伤剂高度敏感,并导致细胞周期检查点激活和细胞凋亡出现缺陷。因此,MDC1/NFBD1似乎是哺乳动物细胞中DNA损伤反应的关键调节因子。