BINDING OF GLUCOCORTICOID RECEPTORS TO MODEL DNA RESPONSE ELEMENTS

被引:3
作者
BENOREPARSONS, M
LIEBMAN, J
WENNOGLE, LP
机构
[1] CIBA GEIGY CORP, DIV RES, 556 MORRIS AVE, SUMMIT, NJ 07901 USA
[2] UNIV MICHIGAN, DEPT NAT SCI, DEARBORN, MI 48128 USA
关键词
GLUCOCORTICOIDS; STEROID-RECEPTOR FAMILY; STEROID-HORMONE; GENE REGULATION; TRANSACTING-FACTORS; MOUSE MAMMARY TUMOR VIRUS; DNA-BINDING;
D O I
10.1002/jcb.240470407
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
DNA sequences were synthesized that contained the consensus 15-base pair glucocorticoid receptor binding site linked to flanking sequences of various lengths. Binding of these synthetic oligomers to glucocorticoid receptor, employing a reconstituted binding system with purified components, indicated that a minimal size of approximately 45 base pairs was necessary to bind the receptor optimally. Sequences containing multiple receptor binding sites competed more effectively for binding. These findings are consistent with recent demonstrations that multiple control elements act synergistically to affect transcriptional control by glucocorticoids and confirm that regions flanking the consensus GRE binding site are instrumental in optimizing binding interactions.
引用
收藏
页码:330 / 336
页数:7
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