Molecular basis for gene-specific transactivation by nuclear receptors

被引:66
作者
Aagaard, Mads M. [1 ]
Siersbaek, Rasmus [1 ]
Mandrup, Susanne [1 ]
机构
[1] Univ So Denmark, Dept Biochem & Mol Biol, DK-5230 Odense M, Denmark
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2011年 / 1812卷 / 08期
关键词
Nuclear receptor specificity; Nuclear receptor structure; DNA binding; Chromatin; Co-factor interaction; DNA looping; DNA-BINDING DOMAIN; HUMAN PROGESTERONE-RECEPTOR; N-TERMINAL DOMAIN; THYROID-HORMONE RECEPTORS; LIGAND-SPECIFIC DYNAMICS; HUMAN ESTROGEN-RECEPTOR; RETINOID-X-RECEPTOR; PPAR-GAMMA-RXR; GLUCOCORTICOID-RECEPTOR; ANDROGEN-RECEPTOR;
D O I
10.1016/j.bbadis.2010.12.018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Nuclear receptors (NRs) are key transcriptional regulators of metazoan physiology and metabolism. Different NRs bind to similar or even identical core response elements; however, they regulate transcription in a highly receptor- and gene-specific manner. These differences in gene activation can most likely be accounted for by mechanisms involving receptor-specific interactions with DNA as well as receptor-specific interactions with protein complexes binding to adjacent and distant DNA sequences. Here, we review key molecular aspects of transactivation by NRs with special emphasis on the recent advances in the molecular mechanisms responsible for receptor- and gene-specific transcriptional activation. This article is part of a Special Issue entitled: Translating nuclear receptors from health to disease. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:824 / 835
页数:12
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