Meng Xiangbing, Liu Jingmei, Shen Zhiyuan
Department of Molecular Genetics and Microbiology, University of New Mexico School of Medicine, Albuquerque, New Mexico 87131-0001, USA.
Cell Cycle. 2004 Mar;3(3):343-8. Epub 2004 Mar 1.
The BCCIP alpha protein was identified as a BRCA2 and CDKN1A (p21, or p21(Waf1/Cip1)) Interacting Protein. It binds to a highly conserved domain proximate to the C-terminus of BRCA2 protein and the C-terminal domain of the CDK-inhibitor p21. Previous reports showed that BCCIP alpha enhances the inhibitory activity of p21 toward CDK2 and that BCCIP alpha inhibits the growth of certain tumor cells. Here we show that a second isoform, BCCIP beta, also binds to p21 and inhibits cell growth. The growth inhibition by BCCIP beta can be partially abrogated in p21 deficient cells. Overexpression of BCCIP beta delays the G1 to S progression and results in an elevated p21 expression. These data suggest BCCIP beta as a new regulator for the G1-S cell cycle progression and cell growth control.
BCCIPα蛋白被鉴定为一种与BRCA2和CDKN1A(p21,即p21(Waf1/Cip1))相互作用的蛋白。它与BRCA2蛋白C端附近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端结构域结合。先前的报道表明,BCCIPα增强了p21对CDK2的抑制活性,并且BCCIPα抑制某些肿瘤细胞的生长。在此我们表明,第二种同种型BCCIPβ也与p21结合并抑制细胞生长。在p21缺陷细胞中,BCCIPβ对生长的抑制作用可部分消除。BCCIPβ的过表达延迟了G1期到S期的进程,并导致p21表达升高。这些数据表明BCCIPβ是G1-S细胞周期进程和细胞生长控制的一种新调节因子。