Nuclear Receptors, RXR, and the Big Bang

被引:1052
作者
Evans, Ronald M. [1 ,2 ]
Mangelsdorf, David J. [1 ,3 ]
机构
[1] Salk Inst Biol Studies, Howard Hughes Med Inst, La Jolla, CA 92037 USA
[2] Salk Inst Biol Studies, La Jolla, CA 92037 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Pharmacol, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
RETINOID-X-RECEPTOR; HUMAN GLUCOCORTICOID-RECEPTOR; THYROID-HORMONE RECEPTORS; BREAST-CANCER CELLS; REV-ERB-ALPHA; TRANSCRIPTIONAL CONTROL; HETERODIMER FORMATION; SIGNALING PATHWAYS; ENERGY-METABOLISM; RESPONSE ELEMENTS;
D O I
10.1016/j.cell.2014.03.012
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
Isolation of genes encoding the receptors for steroids, retinoids, vitamin D, and thyroid hormone and their structural and functional analysis revealed an evolutionarily conserved template for nuclear hormone receptors. This discovery sparked identification of numerous genes encoding related proteins, termed orphan receptors. Characterization of these orphan receptors and, in particular, of the retinoid X receptor (RXR) positioned nuclear receptors at the epicenter of the "Big Bang'' of molecular endocrinology. This Review provides a personal perspective on nuclear receptors and explores their integrated and coordinated signaling networks that are essential for multicellular life, highlighting the RXR heterodimer and its associated ligands and transcriptional mechanism.
引用
收藏
页码:255 / 266
页数:12
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