Therrien M, Wong A M, Rubin G M
Howard Hughes Medical Institute and Department of Molecular and Cell Biology, University of California, Berkeley 94720-3200, USA.
Cell. 1998 Oct 30;95(3):343-53. doi: 10.1016/s0092-8674(00)81766-3.
Kinase suppressor of ras (ksr) is required for efficient signal transmission within the RAS/MAPK cascade. A screen for mutations that modify a ksr-dependent phenotype identified a novel gene, connector enhancer of ksr (cnk), that functions upstream or in parallel to RAF in the RAS pathway. cnk encodes a protein containing several protein-protein interaction domains, suggesting that it brings different signaling molecules together. CNK is required in multiple receptor tyrosine kinase pathways where it appears to be a tyrosine phosphorylation target. Finally, CNK physically interacts with RAF and appears to localize to cell-cell contact regions. Together, these findings suggest that CNK is a novel component of a RAS-dependent signaling pathway that regulates RAF function and/or targets RAF to a specific subcellular compartment upon RAS activation.
Ras激酶抑制因子(ksr)是RAS/丝裂原活化蛋白激酶(MAPK)级联反应中高效信号传导所必需的。一项针对修饰ksr依赖性表型的突变进行的筛选鉴定出一个新基因——ksr连接增强子(cnk),它在RAS途径中位于RAF上游或与其平行发挥作用。cnk编码一种包含多个蛋白质-蛋白质相互作用结构域的蛋白质,这表明它能将不同的信号分子聚集在一起。在多个受体酪氨酸激酶途径中都需要CNK,它似乎是一个酪氨酸磷酸化靶点。最后,CNK与RAF发生物理相互作用,并且似乎定位于细胞间接触区域。总之,这些发现表明CNK是RAS依赖性信号通路的一个新组分,该信号通路在RAS激活时调节RAF功能和/或将RAF靶向特定的亚细胞区室。