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A cytoplasmic inhibitor of the JNK signal transduction pathway.
- 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.
- Subjects :
- Activating Transcription Factor 2
Animals
COS Cells
Carrier Proteins chemistry
Cell Nucleus metabolism
Cell Transformation, Neoplastic
Cells, Cultured
Cloning, Molecular
Cyclic AMP Response Element-Binding Protein metabolism
Cytoplasm metabolism
Fusion Proteins, bcr-abl metabolism
Gene Expression Regulation
JNK Mitogen-Activated Protein Kinases
Mitogen-Activated Protein Kinase 9
Molecular Sequence Data
Phosphorylation
Protein Kinases metabolism
Proto-Oncogene Proteins c-jun metabolism
Recombinant Fusion Proteins metabolism
Transcription Factors metabolism
Transcriptional Activation
Transfection
Calcium-Calmodulin-Dependent Protein Kinases metabolism
Carrier Proteins metabolism
Mitogen-Activated Protein Kinases
Signal Transduction
Subjects
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