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

被引:453
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
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.
引用
收藏
页码:4087 / 4095
页数:9
相关论文
共 61 条
  • [1] LIGAND-DEPENDENT CONFORMATIONAL-CHANGES IN THE PROGESTERONE-RECEPTOR ARE NECESSARY FOR EVENTS THAT FOLLOW DNA-BINDING
    ALLAN, GF
    TSAI, SY
    TSAI, MJ
    OMALLEY, BW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (24) : 11750 - 11754
  • [2] THE ROLE OF JUN, FOS AND THE AP-1 COMPLEX IN CELL-PROLIFERATION AND TRANSFORMATION
    ANGEL, P
    KARIN, M
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1072 (2-3) : 129 - 157
  • [3] CLONING OF HUMAN MINERALOCORTICOID RECEPTOR COMPLEMENTARY-DNA - STRUCTURAL AND FUNCTIONAL KINSHIP WITH THE GLUCOCORTICOID RECEPTOR
    ARRIZA, JL
    WEINBERGER, C
    CERELLI, G
    GLASER, TM
    HANDELIN, BL
    HOUSMAN, DE
    EVANS, RM
    [J]. SCIENCE, 1987, 237 (4812) : 268 - 275
  • [4] THE NEURONAL MINERALOCORTICOID RECEPTOR AS A MEDIATOR OF GLUCOCORTICOID RESPONSE
    ARRIZA, JL
    SIMERLY, RB
    SWANSON, LW
    EVANS, RM
    [J]. NEURON, 1988, 1 (09) : 887 - 900
  • [5] ARRIZA JL, 1991, COLLOQ INSE, V215, P13
  • [6] MODULAR STRUCTURE OF A CHICKEN LYSOZYME SILENCER - INVOLVEMENT OF AN UNUSUAL THYROID-HORMONE RECEPTOR-BINDING SITE
    BANIAHMAD, A
    STEINER, C
    KOHNE, AC
    RENKAWITZ, R
    [J]. CELL, 1990, 61 (03) : 505 - 514
  • [7] MUTUALLY EXCLUSIVE INTERACTION OF THE CCAAT-BINDING FACTOR AND OF A DISPLACEMENT PROTEIN WITH OVERLAPPING SEQUENCES OF A HISTONE GENE PROMOTER
    BARBERIS, A
    SUPERTIFURGA, G
    BUSSLINGER, M
    [J]. CELL, 1987, 50 (03) : 347 - 359
  • [8] GENE-REGULATION BY STEROID-HORMONES
    BEATO, M
    [J]. CELL, 1989, 56 (03) : 335 - 344
  • [9] RXR-ALPHA, A PROMISCUOUS PARTNER OF RETINOIC ACID AND THYROID-HORMONE RECEPTORS
    BUGGE, TH
    POHL, J
    LONNOY, O
    STUNNENBERG, HG
    [J]. EMBO JOURNAL, 1992, 11 (04) : 1409 - 1418
  • [10] 2 NUCLEAR SIGNALING PATHWAYS FOR VITAMIN-D
    CARLBERG, C
    BENDIK, I
    WYSS, A
    MEIER, E
    STURZENBECKER, LJ
    GRIPPO, JF
    HUNZIKER, W
    [J]. NATURE, 1993, 361 (6413) : 657 - 660