Metabolic and chemical architecture of the mammalian circadian clock

被引:22
作者
Laothamatas, Isara [1 ]
Rasmussen, Emil Sjulstok [1 ]
Green, Carla B. [1 ]
Takahashi, Joseph S. [1 ,2 ]
机构
[1] Univ Texas Southwestern Med Ctr, Peter ODonnell Jr Brain Inst, Dept Neurosci, 5323 Harry Hines Blvd, Dallas, TX 75390 USA
[2] Univ Texas Southwestern Med Ctr Dallas, Howard Hughes Med Inst, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
REV-ERB-ALPHA; ROR-GAMMA-T; SMALL-MOLECULE MODULATORS; NUCLEAR RECEPTORS; CRYSTAL-STRUCTURE; RETINOIC ACID; SOCIAL JETLAG; TRANSCRIPTIONAL ARCHITECTURE; POSTTRANSCRIPTIONAL CONTROL; GENE-EXPRESSION;
D O I
10.1016/j.chembiol.2023.08.014
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
Circadian rhythms are endogenous periodic biological processes that occur on a daily timescale. These rhythms are generated by a transcriptional/translational feedback loop that consists of the CLOCKBMAL1 heterodimeric transcriptional activator complex and the PER1/2-CRY1/2-CK1d/epsilon repressive complex. The output pathways of this molecular feedback loop generate circadian rhythmicity in various biological processes. Among these, metabolism is a primary regulatory target of the circadian clock which can also feedback to modulate clock function. This intertwined relationship between circadian rhythms and metabolism makes circadian clock components promising therapeutic targets. Despite this, pharmacological therapeutics that target the circadian clock are relatively rare. In this review, we hope to stimulate interest in chemical chronobiology by providing a comprehensive background on the molecular mechanism of mammalian circadian rhythms and their connection to metabolism, highlighting important studies in the chemical approach to circadian research, and offering our perspectives on future developments in the field.
引用
收藏
页码:1033 / 1052
页数:20
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