Tapon N, Nagata K, Lamarche N, Hall A
MRC Laboratory for Molecular Cell Biology, CRC Oncogene and Signal Transduction Group, University College London, London WC1E 6BT, UK.
EMBO J. 1998 Mar 2;17(5):1395-404. doi: 10.1093/emboj/17.5.1395.
The Rho, Rac and Cdc42 GTPases coordinately regulate the organization of the actin cytoskeleton and the JNK MAP kinase pathway. Mutational analysis of Rac has previously shown that these two activities are mediated by distinct cellular targets, though their identity is not known. Two Rac targets, p65(PAK) and MLK, are ser/thr kinases that have been reported to be capable of activating the JNK pathway. We present evidence that neither is the Rac target mediating JNK activation in Cos-1 cells. We have used yeast two-hybrid selection and identified a new target of Rac, POSH. This protein consists of four SH3 domains and ectopic expression leads to the activation of the JNK pathway and to nuclear translocation of NF-kappaB. When overexpressed in fibroblasts, POSH is a strong inducer of apoptosis. We propose that POSH acts as a scaffold protein and contributes to Rac-induced signal transduction pathways leading to diverse gene transcriptional changes.
Rho、Rac和Cdc42 GTP酶协同调节肌动蛋白细胞骨架的组织以及JNK丝裂原活化蛋白激酶途径。先前对Rac的突变分析表明,这两种活性是由不同的细胞靶点介导的,尽管它们的身份尚不清楚。Rac的两个靶点p65(PAK)和MLK是丝氨酸/苏氨酸激酶,据报道它们能够激活JNK途径。我们提供的证据表明,在Cos-1细胞中,两者都不是介导JNK激活的Rac靶点。我们利用酵母双杂交筛选并鉴定出Rac的一个新靶点POSH。该蛋白由四个SH3结构域组成,异位表达会导致JNK途径的激活以及NF-κB的核转位。当在成纤维细胞中过表达时,POSH是一种强烈的凋亡诱导剂。我们提出,POSH作为一种支架蛋白,有助于Rac诱导的信号转导途径,导致多种基因转录变化。