Modulation of nuclear receptor function by cellular redox poise

被引:20
作者
Carter, Eric L. [1 ]
Ragsdale, Stephen W. [1 ]
机构
[1] Univ Michigan, Dept Biol Chem, Ann Arbor, MI 48109 USA
关键词
Redox; Oxidative stress; Nuclear receptor; Transcription; Hormone; Thiol-disulfide; REV-ERB-ALPHA; HORMONE-BINDING DOMAIN; HUMAN ESTROGEN-RECEPTOR; FREE-RADICAL GENERATION; CHICKEN PROGESTERONE-RECEPTOR; HUMAN GLUCOCORTICOID-RECEPTOR; FINGER TRANSCRIPTION FACTORS; INCREASED OXIDATIVE STRESS; MEDIATED GENE-EXPRESSION; DNA-BINDING;
D O I
10.1016/j.jinorgbio.2014.01.005
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 ligand-responsive transcription factors involved in diverse cellular processes ranging from metabolism to circadian rhythms. This review focuses on NRs that contain redox-active thiol groups, a common feature within the superfamily. We will begin by describing NRs, how they regulate various cellular processes and how binding ligands, corepressors and/or coactivators modulate their activity. We will then describe the general area of redox regulation, especially as it pertains to thiol-disulfide interconversion and the cellular systems that respond to and govern this redox equilibrium. Lastly, we will discuss specific examples of NRs whose activities are regulated by redox-active thiols. Glucocorticoid, estrogen, and the heme-responsive receptor, Rev-erb, will be described in the most detail as they exhibit archetypal redox regulatory mechanisms. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:92 / 103
页数:12
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