COOPERATIVE BINDING OF THE GLUCOCORTICOID RECEPTOR DNA-BINDING DOMAIN IS ONE OF AT LEAST 2 MECHANISMS FOR SYNERGISM

被引:31
作者
BANIAHMAD, C [1 ]
MULLER, M [1 ]
ALTSCHMIED, J [1 ]
RENKAWITZ, R [1 ]
机构
[1] MAX PLANCK INST BIOCHEM, W-8033 MARTINSRIED, GERMANY
关键词
COOPERATIVE DNA-BINDING; DNA-BINDING DOMAIN; GLUCOCORTICOID RECEPTOR; STEROID INDUCTION; SYNERGISM;
D O I
10.1016/0022-2836(91)90202-H
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 induction of responsive genes functions through the synergistic activity of steroid receptor binding sequences with adjacent binding sites either for other transcription factors or for further steroid receptors. Analysis of the human glucocorticoid receptor revealed that the DNA-binding domain of the receptor is sufficient to mediate co-operative binding to adjacent receptor binding sites. This is a novel feature of the domain in addition to its DNA-binding, trans-activating and trans-repressing properties. Chimaeric proteins containing the N- or C-terminal receptor halves fused to the GAL4 DNA-binding domain do not co-operate in DNA-binding, however they do functionally synergize. Thus, at least two mechanisms contribute to the synergism of the human glucocorticoid receptor bound to two adjacent receptor binding sites. © 1991.
引用
收藏
页码:155 / 165
页数:11
相关论文
共 58 条
[21]   CHARACTERIZATION OF RESPONSE ELEMENTS FOR ANDROGENS, GLUCOCORTICOIDS AND PROGESTINS IN MOUSE MAMMARY-TUMOR VIRUS [J].
HAM, J ;
THOMSON, A ;
NEEDHAM, M ;
WEBB, P ;
PARKER, M .
NUCLEIC ACIDS RESEARCH, 1988, 16 (12) :5263-5276
[22]  
HARD T, 1990, BIOCHEMISTRY-US, V29, P5358
[23]   MULTIPLE AND COOPERATIVE TRANS-ACTIVATION DOMAINS OF THE HUMAN GLUCOCORTICOID RECEPTOR [J].
HOLLENBERG, SM ;
EVANS, RM .
CELL, 1988, 55 (05) :899-906
[24]   SUBFRAGMENTS OF THE LARGE TERMINAL REPEAT CAUSE GLUCOCORTICOID-RESPONSIVE EXPRESSION OF MOUSE MAMMARY-TUMOR VIRUS AND OF AN ADJACENT GENE [J].
HYNES, N ;
VANOOYEN, AJJ ;
KENNEDY, N ;
HERRLICH, P ;
PONTA, H ;
GRONER, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (12) :3637-3641
[25]   COOPERATIVITY OF GLUCOCORTICOID RESPONSE ELEMENTS LOCATED FAR UPSTREAM OF THE TYROSINE AMINOTRANSFERASE GENE [J].
JANTZEN, HM ;
STRAHLE, U ;
GLOSS, B ;
STEWART, F ;
SCHMID, W ;
BOSHART, M ;
MIKSICEK, R ;
SCHUTZ, G .
CELL, 1987, 49 (01) :29-38
[26]   SEPARATION OF DNA-BINDING FROM THE TRANSCRIPTION-ACTIVATING FUNCTION OF A EUKARYOTIC REGULATORY PROTEIN [J].
KEEGAN, L ;
GILL, G ;
PTASHNE, M .
SCIENCE, 1986, 231 (4739) :699-704
[27]  
KLEINHITPASS L, 1988, J MOL BIOL, V201, P537
[28]   COMMITMENT AND ACTIVATION AT POL II PROMOTERS - A TAIL OF PROTEIN PROTEIN INTERACTIONS [J].
LEWIN, B .
CELL, 1990, 61 (07) :1161-1164
[29]   MUTUAL TRANSREPRESSION OF FOS AND THE GLUCOCORTICOID RECEPTOR - INVOLVEMENT OF A FUNCTIONAL DOMAIN IN FOS WHICH IS ABSENT IN FOSB [J].
LUCIBELLO, FC ;
SLATER, EP ;
JOOSS, KU ;
BEATO, M ;
MULLER, R .
EMBO JOURNAL, 1990, 9 (09) :2827-2834
[30]   A NEW CLASS OF YEAST TRANSCRIPTIONAL ACTIVATORS [J].
MA, J ;
PTASHNE, M .
CELL, 1987, 51 (01) :113-119