DEVELOPMENTAL REGULATION OF A MURINE T-CELL-SPECIFIC TYROSINE KINASE GENE, TSK

被引:151
作者
HEYECK, SD
BERG, LJ
机构
[1] Cellular/Developmental Biology Dept., Harvard University, Cambridge, MA 02138
关键词
SRC-HOMOLOGY REGION 2 DOMAIN; SRC-HOMOLOGY REGION-3 DOMAIN; THYMUS;
D O I
10.1073/pnas.90.2.669
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Protein-tyrosine kinases have been implicated in signal transduction in T lymphocytes after stimulation of many cell-surface molecules, including the T-cell antigen receptor, CD4, CD8, CD2, CD5, and CD28. Yet the identities of many of these tyrosine kinases remain unknown. We have isolated a murine tyrosine kinase gene, called Tsk for T-cell-specific kinase, that appears to be exclusively expressed in T lymphocytes. The Tsk cDNA clone encodes a polypeptide of 70 kDa, which is similar in sequence to both the src and abl families of tyrosine kinases. Sequence comparisons also indicate that Tsk contains one src-homology region 2 domain and one src-homology 3 domain but lacks the negative regulatory tyrosine (src Tyr-527) common to src-family kinases. In addition, Tsk expression is developmentally regulated. Steady-state Tsk mRNA levels are 5- to 10-fold higher in thymocytes than in peripheral T cells and increase in the thymus during mouse development from neonate to adult. Furthermore, Tsk is expressed in day 14 fetal thymus, suggesting a role for Tsk in early T-lymphocyte differentiation.
引用
收藏
页码:669 / 673
页数:5
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