Kim Hongtae, Chen Junjie, Yu Xiaochun
Department of Therapeutic Radiology, Yale University School of Medicine, Post Office Box 208040, New Haven, CT 06520, USA.
Science. 2007 May 25;316(5828):1202-5. doi: 10.1126/science.1139621.
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.
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。