A direct interaction between JNK1 and CrkII is critical for Rac1-induced JNK activation

被引:51
作者
Girardin, SE [1 ]
Yaniv, M [1 ]
机构
[1] Inst Pasteur, Unite Virus Oncogenes, URA CNRS 1644, F-75724 Paris 15, France
关键词
CTkII; cytoskeleton; JNK1; p130Cas; Rho GTPase;
D O I
10.1093/emboj/20.13.3437
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
CrkII, a cellular homolog of nu -crk, belongs to a family of adaptor proteins that play a central role in signal transduction cascades. We demonstrate that CrkII interacts directly with c-Jun N-terminal kinase 1 (JNK1), A proline-rich sequence of JNK1 is critical for the interaction of the kinase with the N-terminal Src homology 3 (SH3) domain of CrkII. JNK1 is localized with CrkII in membrane ruffles of Crk-over-expressing cells in a Rac1-dependent manner. A JNK1 mutant (K340A) that fails to interact with CrkII is defective in Rac/epidermal growth factor-induced activation, but remains responsive to UVC irradiation. Furthermore, CrkII recruits JNK1 to a p130Cas multiprotein complex where it mag be activated through a hematopoietic progenitor kinase 1- and mitogen-activated protein kinase kinase 4-dependent pathway. Together, the results presented here argue for a new mechanism of regulation of the JNK pathway through the 2CrkII-p130Cas adaptor complex.
引用
收藏
页码:3437 / 3446
页数:10
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