Wang Bin, Hurov Kristen, Hofmann Kay, Elledge Stephen J
Department of Genetics, Howard Hughes Medical Institute, Center for Genetics and Genomics, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
Genes Dev. 2009 Mar 15;23(6):729-39. doi: 10.1101/gad.1770309. Epub 2009 Mar 4.
The ability to sense and respond to DNA damage is critical to maintenance of genomic stability and the prevention of cancer. In this study, we employed a genetic screen to identify a gene, NBA1 (new component of the BRCA1 A complex), that is required for resistance to ionizing radiation. The NBA1 protein localizes to sites of DNA damage and is required for G2/M checkpoint control. Proteomic analysis revealed that NBA1 is a component of the BRCA1 A complex, which also contains Brca1/Bard1, Abra1, RAP80, BRCC36, and BRE. NBA1 is required to maintain BRE and Abra1 abundance and for the recruitment of BRCA1 to sites of DNA damage. In depth bioinformatics analysis revealed that the BRCA1 A complex bears striking similarities to the 19S proteasome complex. Furthermore, we show that four members of the BRCA1-A complex possess a polyubiquitin chain-binding capability, thus forming a complex that might facilitate the deubiquitinating activity of the deubiquitination enzyme BRCC36 or the E3 ligase activity of the BRCA1/BARD1 ligase. These findings provide a new perspective from which to view the BRCA1 A complex.
感知和响应DNA损伤的能力对于维持基因组稳定性和预防癌症至关重要。在本研究中,我们采用基因筛选来鉴定一个基因NBA1(BRCA1 A复合物的新组分),它是抵抗电离辐射所必需的。NBA1蛋白定位于DNA损伤位点,是G2/M期关卡控制所必需的。蛋白质组学分析表明,NBA1是BRCA1 A复合物的一个组分,该复合物还包含Brca1/Bard1、Abra1、RAP80、BRCC36和BRE。维持BRE和Abra1的丰度以及将BRCA1招募到DNA损伤位点需要NBA1。深入的生物信息学分析表明,BRCA1 A复合物与19S蛋白酶体复合物具有显著相似性。此外,我们表明BRCA1 - A复合物的四个成员具有多聚泛素链结合能力,从而形成一个可能促进去泛素化酶BRCC36的去泛素化活性或BRCA1/BARD1连接酶的E3连接酶活性的复合物。这些发现为观察BRCA1 A复合物提供了一个新的视角。