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泛素结合蛋白RAP80介导BRCA1依赖性DNA损伤反应。

Ubiquitin-binding protein RAP80 mediates BRCA1-dependent DNA damage response.

作者信息

Kim Hongtae, Chen Junjie, Yu Xiaochun

机构信息

Department of Therapeutic Radiology, Yale University School of Medicine, Post Office Box 208040, New Haven, CT 06520, USA.

出版信息

Science. 2007 May 25;316(5828):1202-5. doi: 10.1126/science.1139621.

Abstract

Mutations in the breast cancer susceptibility gene 1 (BRCA1) are associated with an increased risk of breast and ovarian cancers. BRCA1 participates in the cellular DNA damage response. We report the identification of receptor-associated protein 80 (RAP80) as a BRCA1-interacting protein in humans. RAP80 contains a tandem ubiquitin-interacting motif domain, which is required for its binding with ubiquitin in vitro and its damage-induced foci formation in vivo. Moreover, RAP80 specifically recruits BRCA1 to DNA damage sites and functions with BRCA1 in G2/M checkpoint control. Together, these results suggest the existence of a ubiquitination-dependent signaling pathway involved in the DNA damage response.

摘要

乳腺癌易感基因1(BRCA1)的突变与乳腺癌和卵巢癌风险增加相关。BRCA1参与细胞DNA损伤反应。我们报告了在人类中鉴定出受体相关蛋白80(RAP80)作为一种与BRCA1相互作用的蛋白。RAP80含有串联泛素相互作用基序结构域,这是其在体外与泛素结合以及在体内损伤诱导的病灶形成所必需的。此外,RAP80特异性地将BRCA1募集到DNA损伤位点,并在G2/M期检查点控制中与BRCA1共同发挥作用。这些结果共同表明存在一条参与DNA损伤反应的泛素化依赖性信号通路。

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