Ishimaru S, Williams R, Clark E, Hanafusa H, Gaul U
Laboratory of Molecular Oncology, The Rockefeller University, 1230 York Avenue, New York, NY 10021, USA.
EMBO J. 1999 Jan 4;18(1):145-55. doi: 10.1093/emboj/18.1.145.
The cellular signal transduction pathways by which C3G, a RAS family guanine nucleotide exchange factor, mediates v-crk transformation are not well understood. Here we report the identification of Drosophila C3G, which, like its human cognate, specifically binds to CRK but not DRK/GRB2 adaptor molecules. During Drosophila development, constitutive membrane binding of C3G, which also occurs during v-crk transformation, results in cell fate changes and overproliferation, mimicking overactivity of the RAS-MAPK pathway. The effects of C3G overactivity can be suppressed by reducing the gene dose of components of the RAS-MAPK pathway and of RAP1. These findings provide the first in vivo evidence that membrane localization of C3G can trigger activation of RAP1 and RAS resulting in the activation of MAPK, one of the hallmarks of v-crk transformation previously thought to be mediated through activation of SOS.
RAS家族鸟嘌呤核苷酸交换因子C3G介导v-crk转化的细胞信号转导途径尚未完全明确。在此,我们报告了果蝇C3G的鉴定结果,它与其人类同源物一样,特异性结合CRK,但不结合DRK/GRB2衔接分子。在果蝇发育过程中,C3G的组成型膜结合(这在v-crk转化过程中也会发生)会导致细胞命运改变和过度增殖,类似于RAS-MAPK途径的过度激活。通过降低RAS-MAPK途径和RAP1组分的基因剂量,可以抑制C3G过度激活的影响。这些发现提供了首个体内证据,表明C3G的膜定位可触发RAP1和RAS的激活,从而导致MAPK的激活,这是v-crk转化的特征之一,此前认为是通过SOS的激活介导的。