Molecular circadian rhythms in central and peripheral clocks in mammals

被引:227
作者
Dardente, Hugues [1 ]
Cermakian, Nicolas [1 ]
机构
[1] McGill Univ, Douglas Hosp, Res Ctr, Dept Psychiat, Montreal, PQ H4H 1R3, Canada
基金
加拿大健康研究院;
关键词
circadian rhythm; clock gene; phosphorylation; transcription; translation; DROSOPHILA PERIOD PROTEIN; SLEEP PHASE SYNDROME; KINASE-I-EPSILON; GLYCOGEN-SYNTHASE KINASE-3-BETA; RECEPTOR ROR-ALPHA; SUPRACHIASMATIC NUCLEUS; GENE-EXPRESSION; MESSENGER-RNA; REV-ERB; POSTTRANSLATIONAL REGULATION;
D O I
10.1080/07420520701283693
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The last decade has seen tremendous progress in our understanding of the organization and function of the circadian clock. A number of so-called clock genes were discovered, and these genes and their protein products were shown to organize into feedback loops to give a near 24 h rhythmicity. However, the mechanism is much more complicated. First, many new clock components have been identified, increasing both our understanding and the overall complexity of the mechanism. Second, there is now evidence that transcription may not play a central role in determining the functioning of the clock: the identification of post-translational modifications of the clock proteins has revealed new levels of control. Finally, chromatin remodeling seems to be crucial in the regulation of the expression of major clock components. This review describes the recent advances in our knowledge of the molecular clockwork in mammals; in particular, the contribution of new clock components and of post-transcriptional and post-translational events to circadian timekeeping are discussed.
引用
收藏
页码:195 / 213
页数:19
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