Shc regulates epidermal growth factor-induced activation of the JNK signaling pathway

被引:54
作者
Hashimoto, A
Kurosaki, M
Gotoh, N
Shibuya, R
Kurosaki, T [1 ]
机构
[1] Kansai Med Univ, Inst Liver Res, Dept Mol Genet, Moriguchi, Osaka 5708506, Japan
[2] Univ Tokyo, Inst Med Sci, Dept Genet, Minato Ku, Tokyo 1080071, Japan
关键词
D O I
10.1074/jbc.274.29.20139
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Two adaptor molecules, Grb2 and Shc, have been implicated in the extracellular signal-regulated kinase (ERK) activation by receptor tyrosine kinases such as the epidermal growth factor receptor (EGFR). Here we show that the EGF-mediated ERK activation is abolished by loss of Grb2, whereas this response is not affected by loss of Shc. Conversely, the EGF-mediated c-Jun N-terminal kinase (JNK) activation is dependent on Shc, but not Grb2. These findings strongly support distinct roles for Grb2 and Shc in controlling ERK and JNK activation after EGF stimulation.
引用
收藏
页码:20139 / 20143
页数:5
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