Williams N G, Roberts T M
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115.
Cancer Metastasis Rev. 1994 Mar;13(1):105-16. doi: 10.1007/BF00690421.
The raf genes encode for a family of cytoplasmic proteins (A-raf, B-raf and c-raf-1) with associated serine/threonine kinase activities. Raf-1 is an important mediator of signals involving cell growth, transformation and differentiation. It is activated in response to a wide variety of extracellular stimuli such as insulin, nerve growth factor (NGF), platelet derived-growth factor (PDGF), and in response to expression of oncogenes, v-src and v-ras, in a cell-specific manner. Recently, the first physiological substrate for Raf-1 protein kinase was identified. Raf-1 was found to phosphorylate and activate Mitogen-Activated Protein Kinase Kinase (MEK), an activator of MAP kinase, thus linking the Raf-1 signaling pathway with that of MAP kinase. Cell specific differences in signalling pathways involving Raf-1 and MAP kinase have also been discovered. Accumulating evidence indicates that membrane tyrosine kinases, ras, Raf-1, MEK and MAP kinase are interconnected via a complex network rather than via a linear pathway involving multiple substrates and feedback loops.
raf基因编码一类具有相关丝氨酸/苏氨酸激酶活性的细胞质蛋白家族(A-raf、B-raf和c-raf-1)。Raf-1是涉及细胞生长、转化和分化信号的重要介质。它可响应多种细胞外刺激而被激活,如胰岛素、神经生长因子(NGF)、血小板衍生生长因子(PDGF),并以细胞特异性方式响应癌基因v-src和v-ras的表达。最近,Raf-1蛋白激酶的首个生理底物被鉴定出来。发现Raf-1可磷酸化并激活丝裂原活化蛋白激酶激酶(MEK),MEK是MAP激酶的激活剂,从而将Raf-1信号通路与MAP激酶信号通路联系起来。还发现了涉及Raf-1和MAP激酶的信号通路中的细胞特异性差异。越来越多的证据表明,膜酪氨酸激酶、ras、Raf-1、MEK和MAP激酶是通过一个复杂网络相互连接的,而不是通过涉及多个底物和反馈环的线性途径。