COT kinase proto-oncogene expression in T cells -: Implication of the JNK/SAPK signal transduction pathway in COT promoter activation

被引:10
作者
Sánchez-Góngora, E
Lisbona, C
de Gregorio, R
Ballester, A
Calvo, V
Pérez-Jurado, L
Alemany, S
机构
[1] Univ Autonoma Madrid, Inst Invest Biomed, Consejo Super Invest Cient, Fac Med, E-28029 Madrid, Spain
[2] Univ Madrid, Hosp La Paz, Serv Genet, Madrid 28046, Spain
关键词
D O I
10.1074/jbc.M000382200
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
COT/Tpl-2 proto oncogene encodes a serine/threonine kinase implicated in cellular activation. In this study we have identified the human COT gene promoter region and three different human COT transcripts. These transcripts, with the same initiation site, display heterogeneity in their 5' untranslated regions and in their subcellular localization. Activation of Jurkat T cells with either calcium ionophore A23187 or alpha CD3 and a phorbol ester increases the levels of the different COT transcripts. Analysis of the 5' flanking region of the human COT gene reveals a unique transcription initiation site and a TATA element 20 nucleotides upstream. Transient expression of COT promoter constructs containing a reporter gene indicates that the transcriptional activity of the 5' flanking region of the COT gene is regulated by T cell-activating signals. Cotransfection of a dominant negative version of SEK-2 abolishes the inducible transcriptional activity of COT promoter, indicating that the inducible expression of the COT gene by T cell activating signals is mediated by the JNK/SAPK signal transduction pathway. All these data indicate stringent regulation of COT kinase proto-oncogene expression.
引用
收藏
页码:31379 / 31386
页数:8
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