Transcriptional and Epigenetic Regulation of Opioid Receptor Genes: Present and Future

被引:52
作者
Wei, Li-Na [1 ]
Loh, Horace H. [1 ]
机构
[1] Univ Minnesota, Sch Med, Dept Pharmacol, Minneapolis, MN 55455 USA
来源
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, VOL 51, 2011 | 2011年 / 51卷
关键词
gene regulation; transcription factor; chromatin remodeling; neuronal differentiation; retinoic acid; SILENCER FACTOR NRSF; MULTIPLE OPIATE RECEPTORS; FACTOR-KAPPA-B; NEURONAL CELLS; MESSENGER-RNA; FUNCTIONAL EXPRESSION; RETINOIC ACID; POSTTRANSCRIPTIONAL REGULATION; CHROMOSOMAL LOCALIZATION; PROXIMAL PROMOTER;
D O I
10.1146/annurev-pharmtox-010510-100605
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Three opioid receptors (ORs) are known: p. opioid receptors (MORs), delta opioid receptors (DORs), and K opioid receptors (KORs). Each is encoded by a distinct gene, and the three OR genes share a highly conserved genomic structure and promoter features, including an absence of TATA boxes and sensitivity to extracellular stimuli and epigenetic regulation. However, each of the genes is differentially expressed. Transcriptional regulation engages both basal and regulated transcriptional machineries and employs activating and silencing mechanisms. In retinoic acid-induced neuronal differentiation, the opioid receptor genes undergo drastically different chromatin remodeling processes and display varied patterns of epigenetic marks. Regulation of KOR expression is distinctly complex, and KOR exerts a unique function in neurite extension, indicating that KOR is not simply a pharmacological cousin of MOR and DOR. As the expression of OR proteins is ultimately controlled by extensive posttranscriptional processing, the pharmacological implication of OR gene regulation at the transcriptional level remains to be determined.
引用
收藏
页码:75 / 97
页数:23
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