Kuroda S, Fukata M, Nakagawa M, Fujii K, Nakamura T, Ookubo T, Izawa I, Nagase T, Nomura N, Tani H, Shoji I, Matsuura Y, Yonehara S, Kaibuchi K
Division of Signal Transduction, Nara Institute of Science and Technology, Ikoma 630-0101, Japan.
Science. 1998 Aug 7;281(5378):832-5. doi: 10.1126/science.281.5378.832.
The small guanosine triphosphatases (GTPases) Cdc42 and Rac1 regulate E-cadherin-mediated cell-cell adhesion. IQGAP1, a target of Cdc42 and Rac1, was localized with E-cadherin and beta-catenin at sites of cell-cell contact in mouse L fibroblasts expressing E-cadherin (EL cells), and interacted with E-cadherin and beta-catenin both in vivo and in vitro. IQGAP1 induced the dissociation of alpha-catenin from a cadherin-catenin complex in vitro and in vivo. Overexpression of IQGAP1 in EL cells, but not in L cells expressing an E-cadherin-alpha-catenin chimeric protein, resulted in a decrease in E-cadherin-mediated cell-cell adhesive activity. Thus, IQGAP1, acting downstream of Cdc42 and Rac1, appears to regulate cell-cell adhesion through the cadherin-catenin pathway.
小GTP酶(GTPases)Cdc42和Rac1调节E-钙黏蛋白介导的细胞间黏附。IQGAP1是Cdc42和Rac1的一个靶点,在表达E-钙黏蛋白的小鼠L成纤维细胞(EL细胞)的细胞间接触位点与E-钙黏蛋白和β-连环蛋白共定位,并在体内和体外与E-钙黏蛋白和β-连环蛋白相互作用。IQGAP1在体内和体外均可诱导α-连环蛋白从钙黏蛋白-连环蛋白复合物中解离。IQGAP1在EL细胞中过表达,但在表达E-钙黏蛋白-α-连环蛋白嵌合蛋白的L细胞中过表达则不会导致E-钙黏蛋白介导的细胞间黏附活性降低。因此,IQGAP1作为Cdc42和Rac1的下游分子,似乎通过钙黏蛋白-连环蛋白途径调节细胞间黏附。