TRANSCRIPTIONAL INTERFERENCE BETWEEN C-JUN AND THE GLUCOCORTICOID RECEPTOR - MUTUAL INHIBITION OF DNA-BINDING DUE TO DIRECT PROTEIN PROTEIN-INTERACTION

被引:1516
作者
YANGYEN, HF
CHAMBARD, JC
SUN, YL
SMEAL, T
SCHMIDT, TJ
DROUIN, J
KARIN, M
机构
[1] UNIV CALIF SAN DIEGO, SCH MED, CTR MOLEC GENET, DEPT BIOL, LA JOLLA, CA 92093 USA
[2] INST RECH CLIN MONTREAL, MONTREAL H2W 1R7, QUEBEC, CANADA
[3] UNIV IOWA, DEPT PHYSIOL & BIOPHYS, IOWA CITY, IA 52242 USA
关键词
D O I
10.1016/0092-8674(90)90396-V
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
Glucocorticoids are potent inhibitors of collagenase induction by phorbol esters and inflammatory mediators. The target for this negative effect is the AP-1 site within the collagenase promoter, which also mediates its induction. Negative regulation is due to repression of AP-1 activity by the glucocorticoid receptor (GCR). While the GCR is a potent inhibitor of AP-1 activity (Jun/Fos), both c-Jun and c-Fos are potent repressors of GCR activity. In vitro experiments using purified GCR and c-Jun proteins suggest that mutual repression is due to direct interaction between the two. Direct interaction between GCR and either c-Jun or c-Fos is demonstrated by cross-linking and coimmunoprecipitation. These findings reveal a cross talk between two major signal transduction systems used to control gene transcription in response to extracellular stimuli, and a novel mechanism for transcriptional repression. © 1990.
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页码:1205 / 1215
页数:11
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