Meng Xiangbing, Lu Huimei, Shen Zhiyuan
University of New Mexico School of Medicine, Department of Molecular Genetics and Microbiology, Albuquerque, New Mexico 87131-000, USA.
Cell Cycle. 2004 Nov;3(11):1457-62. doi: 10.4161/cc.3.11.1213. Epub 2004 Nov 8.
The BCCIP protein is a BRCA2 and CDKN1A (p21(Waf1/Cip1)) Interacting Protein, which binds to a highly conserved domain of BRCA2, and a C-terminal domain of the CDK-inhibitor p21. We have previously reported that overexpression of BCCIP increases p21 mRNA and protein levels, and inhibits G(1) to S progression. In this report, we show that a partial shutdown of BCCIP expression by RNA interference reduces p21 levels and impairs G(1)/S checkpoint activation in response to ionizing radiation in HT1080 cells. We further show that the regulation of p21 expression by BCCIP is dependent on p53, and BCCIP regulates p53 transcription activity. These data provide a new mechanism by which BCCIP regulates p21 functions.
BCCIP蛋白是一种与BRCA2和CDKN1A(p21(Waf1/Cip1))相互作用的蛋白,它与BRCA2的一个高度保守结构域以及细胞周期蛋白依赖性激酶抑制剂p21的C末端结构域结合。我们之前报道过,BCCIP的过表达会增加p21的mRNA和蛋白水平,并抑制G1期到S期的进程。在本报告中,我们表明,通过RNA干扰使BCCIP表达部分关闭会降低p21水平,并损害HT1080细胞中对电离辐射的G1/S检查点激活。我们进一步表明,BCCIP对p21表达的调节依赖于p53,并且BCCIP调节p53的转录活性。这些数据提供了一种BCCIP调节p21功能的新机制。