Rodriguez-Viciana P, Warne P H, Dhand R, Vanhaesebroeck B, Gout I, Fry M J, Waterfield M D, Downward J
Imperial Cancer Research Fund, London, UK.
Nature. 1994 Aug 18;370(6490):527-32. doi: 10.1038/370527a0.
Ras (p21ras) interacts directly with the catalytic subunit of phosphatidylinositol-3-OH kinase in a GTP-dependent manner through the Ras effector site. In vivo, dominant negative Ras mutant N17 inhibits growth factor induced production of 3' phosphorylated phosphoinositides in PC12 cells, and transfection of Ras, but not Raf, into COS cells results in a large elevation in the level of these lipids. Therefore Ras can probably regulate phosphatidylinositol-3-OH kinase, providing a point of divergence in signalling pathways downstream of Ras.
Ras(p21ras)通过Ras效应位点以GTP依赖的方式直接与磷脂酰肌醇-3-OH激酶的催化亚基相互作用。在体内,显性负性Ras突变体N17抑制生长因子诱导的PC12细胞中3'磷酸化磷脂酰肌醇的产生,并且将Ras而非Raf转染到COS细胞中会导致这些脂质水平大幅升高。因此,Ras可能调节磷脂酰肌醇-3-OH激酶,这在Ras下游的信号通路中提供了一个分歧点。