Li B Q, Kaplan D, Kung H F, Kamata T
Biological Carcinogenesis and Development Program, Program Resources, Inc./DynCorp, Frederick, MD 21702.
Science. 1992 Jun 5;256(5062):1456-9. doi: 10.1126/science.1604323.
The biological activity of Ras proteins is thought to be controlled by the guanine nucleotide exchange factor and the guanosine triphosphatase activating protein (GAP). Treatment of rat pheochromocytoma PC-12 cells with nerve growth factor (NGF) increased the amount of active Ras guanosine triphosphate complex and stimulated the activities of both the guanine nucleotide exchange factor and GAP. In PC-12 cells that overexpressed the tyrosine kinase encoded by the trk proto-oncogene (a component of the high-affinity NGF receptor), the NGF-induced activation of the regulatory proteins was potentiated. These results suggest that the NGF receptor system enhances the activities of both the guanine nucleotide exchange factor and GAP and that the activation of Ras might be controlled by the balance in activity between these two regulatory proteins.
Ras蛋白的生物活性被认为受鸟嘌呤核苷酸交换因子和鸟苷三磷酸酶激活蛋白(GAP)调控。用神经生长因子(NGF)处理大鼠嗜铬细胞瘤PC-12细胞可增加活性Ras鸟苷三磷酸复合物的量,并刺激鸟嘌呤核苷酸交换因子和GAP的活性。在过表达trk原癌基因(高亲和力NGF受体的一个组分)编码的酪氨酸激酶的PC-12细胞中,NGF诱导的调节蛋白激活作用增强。这些结果表明,NGF受体系统增强了鸟嘌呤核苷酸交换因子和GAP的活性,并且Ras的激活可能受这两种调节蛋白活性平衡的控制。