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A cytoplasmic inhibitor of the JNK signal transduction pathway.

Authors :
Dickens M
Rogers JS
Cavanagh J
Raitano A
Xia Z
Halpern JR
Greenberg ME
Sawyers CL
Davis RJ
Source :
Science (New York, N.Y.) [Science] 1997 Aug 01; Vol. 277 (5326), pp. 693-6.
Publication Year :
1997

Abstract

The c-Jun amino-terminal kinase (JNK) is a member of the stress-activated group of mitogen-activated protein (MAP) kinases that are implicated in the control of cell growth. A murine cytoplasmic protein that binds specifically to JNK [the JNK interacting protein-1 (JIP-1)] was characterized and cloned. JIP-1 caused cytoplasmic retention of JNK and inhibition of JNK-regulated gene expression. In addition, JIP-1 suppressed the effects of the JNK signaling pathway on cellular proliferation, including transformation by the Bcr-Abl oncogene. This analysis identifies JIP-1 as a specific inhibitor of the JNK signal transduction pathway and establishes protein targeting as a mechanism that regulates signaling by stress-activated MAP kinases.

Details

Language :
English
ISSN :
0036-8075
Volume :
277
Issue :
5326
Database :
MEDLINE
Journal :
Science (New York, N.Y.)
Publication Type :
Academic Journal
Accession number :
9235893
Full Text :
https://doi.org/10.1126/science.277.5326.693