Schwartzberg P L
Laboratory of Genetic Disease Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892-4472, USA.
Oncogene. 1998 Sep 17;17(11 Reviews):1463-8. doi: 10.1038/sj.onc.1202176.
c-src was first isolated as the normal cellular homologue of v-src, the transforming gene of Rous Sarcoma virus (Stehelin et al., 1976). As the first proto-oncogene described and one of the first molecules demonstrated to have tyrosine kinase activity, Src has provided a prototype for understanding signal transduction involving tyrosine phosphorylation. Comparison between c-src and activated or transforming mutants of Src including v-src, combined with recent data on the structure of Src family kinases has provided new insight into their regulation. In this review, I will discuss the function of the various domains of Src in light of these mutational and structural studies.
c-src最初作为Rous肉瘤病毒的转化基因v-src的正常细胞同源物被分离出来(斯特赫林等人,1976年)。作为第一个被描述的原癌基因以及最早被证明具有酪氨酸激酶活性的分子之一,Src为理解涉及酪氨酸磷酸化的信号转导提供了一个原型。c-src与Src的激活或转化突变体(包括v-src)之间的比较,结合最近关于Src家族激酶结构的数据,为它们的调控提供了新的见解。在这篇综述中,我将根据这些突变和结构研究来讨论Src各个结构域的功能。