Perfect timing: Epigenetic regulation of the circadian clock

被引:41
|
作者
Ripperger, Juergen A. [1 ]
Merrow, Martha [2 ]
机构
[1] Univ Fribourg, Dept Biol, Biochem Unit, Fac Sci, CH-1700 Fribourg, Switzerland
[2] Univ Groningen, Fac Math & Nat Sci, Dept Mol & Genet Chronobiol, Groningen, Netherlands
关键词
Chromatin; Methylation; Demethylation; Hysteresis; Histone; HISTONE H3; GENE-EXPRESSION; PROMOTER METHYLATION; CELL-DIVISION; DNA-BINDING; LYSINE; 9; TRANSCRIPTION; REPRESSION; ACETYLATION; PROTEINS;
D O I
10.1016/j.febslet.2011.04.047
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
In mammals, higher order chromatin structures are critical for downsizing the genome (packaging) so that the nucleus can be small. The adjustable density of chromatin also regulates gene expression, thus this post-genetic molecular mechanism is one of the routes by which phenotype is shaped. Phenotypes that arise without a concomitant mutation of the underlying genome are termed epigenetic phenomena. Here we discuss epigenetic phenomena from histone and DNA modification as it pertains to the dynamic regulatory processes of the circadian clock. Epigenetic phenomena certainly explain some regulatory aspects of the mammalian circadian oscillator. (C) 2011 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:1406 / 1411
页数:6
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