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SOCS-1/JAB/SSI-1 can bind to and suppress Tec protein-tyrosine kinase.
- Source :
-
The Journal of biological chemistry [J Biol Chem] 1997 Oct 24; Vol. 272 (43), pp. 27178-82. - Publication Year :
- 1997
-
Abstract
- Tec is the prototype of a recently emerging subfamily among nonreceptor type protein-tyrosine kinases and is known to become tyrosine-phosphorylated and activated by a wide range of cytokine stimulations in hematopoietic cells. Although Tec was recently shown to be involved in the cytokine-driven activation mechanism of c-fos transcription, it is yet obscure how Tec relays the signals from cell surface receptors to the nucleus. To identify signaling molecules acting downstream of Tec, we have looked for Tec-interacting proteins (TIPs) by using the yeast two-hybrid system. Here we report the identification and characterization of a novel protein, TIP3, which has been simultaneously identified by other groups as SOCS-1, JAB, or SSI-1. TIP3 carries one Src homology 2 domain with a sequence similarity to that of CIS. In 293 cells, TIP3 associates with Tec and suppresses its kinase activity. Interestingly, TIP3 can also down-regulate the activity of Jak2 but not that of Lyn. We propose that SOCS-1/JAB/SSI-1/TIP3 is a novel type of negative regulator to a subset of protein-tyrosine kinases.
- Subjects :
- Amino Acid Sequence
Animals
B-Lymphocytes
Base Sequence
Carrier Proteins biosynthesis
Carrier Proteins chemistry
Cell Line
Gene Library
Genes, fos
Humans
Janus Kinase 2
Molecular Sequence Data
Promoter Regions, Genetic
Protein-Tyrosine Kinases chemistry
Recombinant Proteins biosynthesis
Recombinant Proteins chemistry
Recombinant Proteins metabolism
Suppressor of Cytokine Signaling 1 Protein
Suppressor of Cytokine Signaling Proteins
Transfection
src Homology Domains
Carrier Proteins metabolism
Intracellular Signaling Peptides and Proteins
Protein-Tyrosine Kinases antagonists & inhibitors
Protein-Tyrosine Kinases metabolism
Proto-Oncogene Proteins
Repressor Proteins
Subjects
Details
- Language :
- English
- ISSN :
- 0021-9258
- Volume :
- 272
- Issue :
- 43
- Database :
- MEDLINE
- Journal :
- The Journal of biological chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 9341160
- Full Text :
- https://doi.org/10.1074/jbc.272.43.27178