Role of Crk oncogene product in physiologic signaling

被引:63
作者
Kiyokawa, E
Mochizuki, N
Kurata, T
Matsuda, M [1 ]
机构
[1] Int Med Ctr Japan, Natl Inst Infect Dis, Dept Pathol, Shinjuku Ku, Tokyo 1628655, Japan
[2] Int Med Ctr Japan, Res Inst, Dept Pathol, Shinjuku Ku, Tokyo 1628655, Japan
来源
CRITICAL REVIEWS IN ONCOGENESIS | 1997年 / 8卷 / 04期
关键词
v-Crk; c-Crk; CrkII; CrkI; CrkL; oncogene; SH2; SH3;
D O I
10.1615/CritRevOncog.v8.i4.30
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
v-Crk is a member of the family of adaptor-type signaling molecules that consist mostly of SH2 and SH3 domains. The cellular homologs of v-Crk includes CrkI, CrkII, and CrkL; these have been isolated from species ranging from lower vertebrates to man. Crk-family proteins are involved in a variety of signaling cascades such as those of growth factor receptor, integrin, T-cell receptor, B-cell antigen receptor, and cytokines. It has been postulated that the primary function of Crk is to recruit cytoplasmic proteins in the vicinity of tyrosine kinases through SH2-phosphotyrosine interaction. Thus, the output from Crk depends on the SH3-binding proteins, which include the C3G guanine nucleotide exchange protein for Rap1, Abl tyrosine kinase, DOCK180, and the Sos guanine nucleotide exchange protein for Ras. The variety of the Crk-binding proteins indicate the pleiotropic function of Crk.
引用
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页码:329 / 342
页数:14
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