The nuclear receptor superfamily: A structural perspective

被引:290
作者
Weikum, Emily R. [1 ]
Liu, Xu [1 ]
Ortlund, Eric A. [1 ]
机构
[1] Emory Sch Med, Dept Biochem, Atlanta, GA 30322 USA
基金
美国国家卫生研究院;
关键词
nuclear receptor; ligand binding domain; DNA binding domain; co-regulator; transactivation; transrepression; LIGAND-BINDING DOMAIN; PROLIFERATOR-ACTIVATED RECEPTOR; SINGLE-MOLECULE ANALYSIS; RETINOIC ACID RECEPTORS; COREPRESSOR N-COR; DNA-BINDING; GLUCOCORTICOID-RECEPTOR; CRYSTAL-STRUCTURE; STEROID-RECEPTOR; PPAR-GAMMA;
D O I
10.1002/pro.3496
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
Nuclear receptors (NRs) are a family of transcription factors that regulate numerous physiological processes such as metabolism, reproduction, inflammation, as well as the circadian rhythm. NRs sense changes in lipid metabolite levels to drive differential gene expression, producing distinct physiologic effects. This is an allosteric process whereby binding a cognate ligand and specific DNA sequences drives the recruitment of diverse transcriptional co-regulators at chromatin and ultimately transactivation or transrepression of target genes. Dysregulation of NR signaling leads to various malignances, metabolic disorders, and inflammatory disease. Given their important role in physiology and ability to respond to small lipophilic ligands, NRs have emerged as valuable therapeutic targets. Here, we summarize and discuss the recent progress on understanding the complex mechanism of action of NRs, primarily from a structural perspective. Finally, we suggest future studies to improve our understanding of NR signaling and better design drugs by integrating multiple structural and biophysical approaches.
引用
收藏
页码:1876 / 1892
页数:17
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