Cheng S H, Harvey R, Espino P C, Semba K, Yamamoto T, Toyoshima K, Smith A E
Laboratory of Cellular Regulation, Integrated Genetics Inc., Framingham, MA 01701.
EMBO J. 1988 Dec 1;7(12):3845-55. doi: 10.1002/j.1460-2075.1988.tb03270.x.
The c-fyn proto-oncogene is a member of a family of closely related genes of which c-src is the prototype. Using peptide antibodies which had been raised against sequences predicted to be specific for the human c-fyn gene product, the c-fyn protein was identified. It is a tyrosine kinase with apparent mol. wt of 59 kd that is also phosphorylated and myristylated. Like pp60c-src and pp62c-yes, pp59c-fyn is able to form a stable complex with middle-T antigen, the transforming protein of polyomavirus. The transformation-defective middle-T mutant NG59, which is unable to associate stably with pp60c-src does not associate with pp59c-fyn. In contrast to pp60c-src, complex formation with middle-T antigen does not lead to a significant increase in the tyrosine kinase activity of pp59c-fyn. These findings lead us to suggest that middle-T mediated transformation may be a consequence of the deregulation of several members of the src-family of protein tyrosine kinases.
原癌基因c-fyn是一个紧密相关基因家族的成员,其中c-src是原型。使用针对预测为人c-fyn基因产物特异性序列产生的肽抗体,鉴定出了c-fyn蛋白。它是一种酪氨酸激酶,表观分子量为59kd,也被磷酸化和豆蔻酰化。与pp60c-src和pp62c-yes一样,pp59c-fyn能够与多瘤病毒的转化蛋白中间T抗原形成稳定的复合物。转化缺陷型中间T突变体NG59不能与pp60c-src稳定结合,也不能与pp59c-fyn结合。与pp60c-src不同,与中间T抗原形成复合物不会导致pp59c-fyn的酪氨酸激酶活性显著增加。这些发现使我们认为,中间T介导的转化可能是蛋白酪氨酸激酶src家族多个成员失调的结果。