SOCS-1/JAB/SSI-1 can bind to and suppress Tec protein-tyrosine kinase

被引:99
作者
Ohya, K
Kajigaya, S
Yamashita, Y
Miyazato, A
Hatake, K
Miura, Y
Ikeda, U
Shimada, K
Ozawa, K
Mano, H
机构
[1] JICHI MED SCH, DEPT MOL BIOL, MINAMI KAWACHI, TOCHIGI 32904, JAPAN
[2] JICHI MED SCH, DIV CARDIOL, MINAMI KAWACHI, TOCHIGI 32904, JAPAN
[3] JICHI MED SCH, DIV HEMATOL, MINAMI KAWACHI, TOCHIGI 32904, JAPAN
[4] NHLBI, HEMATOL BRANCH, NIH, BETHESDA, MD 20892 USA
关键词
D O I
10.1074/jbc.272.43.27178
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
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-l. TIP3 carries one Src homology 2 domain with a sequence similarity to that of CIS. In 293 cells, TIPB associates with Tec and suppresses its kinase activity. Interestingly, TIPB 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.
引用
收藏
页码:27178 / 27182
页数:5
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