Han J, Luby-Phelps K, Das B, Shu X, Xia Y, Mosteller R D, Krishna U M, Falck J R, White M A, Broek D
Department of Biochemistry and Molecular Biology, Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, CA 90033-0800, USA.
Science. 1998 Jan 23;279(5350):558-60. doi: 10.1126/science.279.5350.558.
Mitogen stimulation of cytoskeletal changes and c-jun amino-terminal kinases is mediated by Rac small guanine nucleotide-binding proteins. Vav, a guanosine diphosphate (GDP)-guanosine triphosphate (GTP) exchange factor for Rac that stimulates the exchange of bound GDP for GTP, bound to and was directly controlled by substrates and products of phosphoinositide (PI) 3-kinase. The PI 3-kinase substrate phosphatidylinositol-4,5-bisphosphate inhibited activation of Vav by the tyrosine kinase Lck, whereas the product phosphatidylinositol-3,4,5-trisphosphate enhanced phosphorylation and activation of Vav by Lck. Control of Vav in response to mitogens by the products of PI 3-kinase suggests a mechanism for Ras-dependent activation of Rac.
有丝分裂原刺激引起的细胞骨架变化和c-jun氨基末端激酶是由Rac小GTP结合蛋白介导的。Vav是一种Rac的鸟苷二磷酸(GDP)-鸟苷三磷酸(GTP)交换因子,可刺激结合的GDP与GTP进行交换,它与磷脂酰肌醇(PI)3激酶的底物和产物结合并直接受其控制。PI 3激酶底物磷脂酰肌醇-4,5-二磷酸抑制酪氨酸激酶Lck对Vav的激活,而产物磷脂酰肌醇-3,4,5-三磷酸增强Lck对Vav的磷酸化和激活作用。PI 3激酶产物对有丝分裂原刺激下Vav的调控提示了一种Ras依赖的Rac激活机制。