López-Barahona M, Bustelo X R, Barbacid M
Department of Molecular Oncology, Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08543-4000, USA.
Oncogene. 1996 Feb 1;12(3):463-70.
TC21 is a highly oncogenic member of the Ras superfamily of small GTP binding proteins. We have used the yeast two hybrid system to identify proteins that interact with an oncogenic form of the TC21 protein. cDNA clones encoding the carboxy-terminal region of the RalGDS protein were isolated from human B-cell and HeLa cDNA libraries. RalGDS is an exchange factor that stimulates GDP dissociation from Ral, another member of the Ras superfamily of proteins. The interaction between RalGDS to TC21 is direct and appears to be mediated by the effector domain of TC21 and the carboxy-terminal region of RalGDS. Moreover, RalGDS only binds to TC21 in its active, GTP-loaded configuration. These results suggest that RalGDS might be an effector molecule for TC21 and may participate in cross-talking between Ral and TC21 signalling pathways.
TC21是小GTP结合蛋白Ras超家族中一个具有高度致癌性的成员。我们利用酵母双杂交系统来鉴定与致癌形式的TC21蛋白相互作用的蛋白质。从人B细胞和HeLa cDNA文库中分离出编码RalGDS蛋白羧基末端区域的cDNA克隆。RalGDS是一种交换因子,可刺激GDP从Ral上解离,Ral是Ras超家族蛋白中的另一个成员。RalGDS与TC21之间的相互作用是直接的,似乎是由TC21的效应结构域和RalGDS的羧基末端区域介导的。此外,RalGDS仅在其活性的、加载GTP的构象下与TC21结合。这些结果表明,RalGDS可能是TC21的效应分子,可能参与Ral和TC21信号通路之间的相互作用。