Ravichandran K S, Lee K K, Songyang Z, Cantley L C, Burn P, Burakoff S J
Division of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA.
Science. 1993 Nov 5;262(5135):902-5. doi: 10.1126/science.8235613.
The shc oncogene product is tyrosine-phosphorylated by Src family kinases and after its phosphorylation interacts with the adapter protein Grb2 (growth factor receptor-bound protein 2). In turn, Grb2 interacts with the guanine nucleotide exchange factor for Ras, mSOS. Because several Src family kinases participate in T cell activation and Shc functions upstream of Ras, the role of Shc in T cell signaling was examined. Shc was phosphorylated on tyrosine after activation through the T cell receptor (TCR), and subsequently interacted with Grb2 and mSOS. The Src homology region 2 (SH2) domain of Shc directly interacted with the tyrosine-phosphorylated zeta chain of the TCR. Thus, Shc may couple TCR activation to the Ras signaling pathway.
Shc癌基因产物被Src家族激酶磷酸化酪氨酸,磷酸化后与衔接蛋白Grb2(生长因子受体结合蛋白2)相互作用。反过来,Grb2与Ras的鸟嘌呤核苷酸交换因子mSOS相互作用。由于几种Src家族激酶参与T细胞活化且Shc在Ras上游发挥作用,因此研究了Shc在T细胞信号传导中的作用。通过T细胞受体(TCR)激活后,Shc的酪氨酸被磷酸化,随后与Grb2和mSOS相互作用。Shc的Src同源区域2(SH2)结构域直接与TCR的酪氨酸磷酸化ζ链相互作用。因此,Shc可能将TCR激活与Ras信号通路偶联起来。