Protein kinase C μ selectively activates the mitogen-activated protein kinase (MAPK) p42 pathway

被引:56
作者
Hausser, A
Storz, P
Hübner, S
Braendlin, I
Martinez-Moya, M
Link, G
Johannes, FJ [1 ]
机构
[1] Fraunhofer Inst Interfacial Engn & Biotechnol, D-70569 Stuttgart, Germany
[2] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Dept Pathol, Boston, MA USA
[3] Univ Stuttgart, Inst Cell Biol & Immunol, D-70569 Stuttgart, Germany
关键词
protein kinase C mu; mitogen-activated protein kinase; p42; serum response element;
D O I
10.1016/S0014-5793(01)02219-0
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
Here we show that human protein kinase C mu (PKC mu) activates the mitogen-activated protein kinase (MAPK). Transient expression of constitutive active PKC mu leads to an activation of Raf-1 kinase as demonstrated by in vitro phosphorylation of MAPK, PKC mu enhances transcriptional activity of a basal thymidine kinase promotor containing serum response elements (SREs) as shown by luciferase reporter gene assays. SRE driven gene activation by PKC mu is triggered by the Elk-1 ternary complex factor. PKC mu -mediated activation of SRE driven transcription can be inhibited by the MEK1 inhibitor PD98059, In contrast to the activation of the p42/ERK1 MAPK cascade, transient expression of constitutive active PKC mu does neither affect c-jun N-terminal kinase nor p38 MAPK. (C) 2001 Federation of European Biochemical Societies, Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:39 / +
页数:7
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