Suppr超能文献

MDC1/NFBD1:高等真核生物中DNA损伤反应的关键调节因子。

MDC1/NFBD1: a key regulator of the DNA damage response in higher eukaryotes.

作者信息

Stucki Manuel, Jackson Stephen P

机构信息

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.

出版信息

DNA Repair (Amst). 2004 Aug-Sep;3(8-9):953-7. doi: 10.1016/j.dnarep.2004.03.007.

Abstract

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.

摘要

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验