Mayol X, Graña X, Baldi A, Sang N, Hu Q, Giordano A
Fels Institute for Cancer Research and Molecular Biology, Temple University, School of Medicine, Philadelphia, PA 19140.
Oncogene. 1993 Sep;8(9):2561-6.
The product of the retinoblastoma tumor suppressor gene (pRb) and p107 share a high degree of structural homology in the pocket region, which is thought to play a primary role in the function of these proteins. It is conceivable that there exists a larger family of cellular proteins containing this pocket region. In this communication, we report cloning of a new human cDNA encoding a polypeptide that shows a high level of identity with pRb and p107 and possesses a pocket region. We have named it pRb2. From the deduced amino acid sequence, pRb2 has a predicted molecular weight of approximately 120 kD and its in vitro translated product binds to the adenovirus E1A protein. Due to its size, pRb2 may correspond to p130, which has previously been shown by us to interact with the transforming region of E1A in in vivo studies. Interestingly, pRb2 fails to bind an E1A mutant in the transforming domain 2 suggesting that pRb2 is involved in the transforming capacity of E1A.
视网膜母细胞瘤抑癌基因(pRb)的产物与p107在口袋区域具有高度的结构同源性,该区域被认为在这些蛋白质的功能中起主要作用。可以想象,存在一个包含该口袋区域的更大的细胞蛋白家族。在本通讯中,我们报告了一个新的人类cDNA的克隆,该cDNA编码一种与pRb和p107具有高度同源性且拥有口袋区域的多肽。我们将其命名为pRb2。根据推导的氨基酸序列,pRb2的预测分子量约为120 kD,其体外翻译产物与腺病毒E1A蛋白结合。由于其大小,pRb2可能对应于p130,我们之前在体内研究中已表明p130与E1A的转化区域相互作用。有趣的是,pRb2不能与转化域2中的E1A突变体结合,这表明pRb2参与了E1A的转化能力。