A DISTINCT MODULATING DOMAIN IN GLUCOCORTICOID RECEPTOR MONOMERS IN THE REPRESSION OF ACTIVITY OF THE TRANSCRIPTION FACTOR AP-1

被引:451
|
作者
HECK, S [1 ]
KULLMANN, M [1 ]
GAST, A [1 ]
PONTA, H [1 ]
RAHMSDORF, HJ [1 ]
HERRLICH, P [1 ]
CATO, ACB [1 ]
机构
[1] KERNFORSCHUNGSZENTRUM KARLSRUHE GMBH, INST GENET, D-76021 KARLSRUHE, GERMANY
来源
EMBO JOURNAL | 1994年 / 13卷 / 17期
关键词
AP-1; D-LOOP; MINERALOCORTICOID RECEPTOR; TRANSREPRESSION; TRANSACTIVATION; ZINC FINGER REGION;
D O I
10.1002/j.1460-2075.1994.tb06726.x
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
Steroid receptors activate and repress genes. An important class of genes that they repress is controled by the transcription factor AP-1. The activity of AP-1 is inhibited by the receptor, a mechanism exploited for the therapy of various forms of pathological hyperproliferation in humans. We show here by point mutations in the DNA binding domain and by the choice of steroid ligands that repression of AP-1 activity and transactivation functions of the glucocorticoid receptor (GR) are separable entities. While DNA binding and activation of glucocorticoid-regulated promoters require GR dimerization, we present data that suggest that repression is a function of GR monomers.
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页码:4087 / 4095
页数:9
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