Circadian behavior is light-reprogrammed by plastic DNA methylation

被引:191
作者
Azzi, Abdelhalim [1 ]
Dallmann, Robert [1 ]
Casserly, Alison [1 ]
Rehrauer, Hubert [2 ]
Patrignani, Andrea [2 ]
Maier, Bert [3 ]
Kramer, Achim [3 ]
Brown, Steven A. [1 ]
机构
[1] Univ Zurich, Inst Pharmacol & Toxicol, Zurich, Switzerland
[2] Univ Zurich, Funct Genom Ctr, Zurich, Switzerland
[3] Charite, Inst Med Immunol, Lab Chronobiol, D-13353 Berlin, Germany
基金
瑞士国家科学基金会;
关键词
MEMORY FORMATION; HUMAN-CELLS; CLOCK; DEMETHYLATION; EXPRESSION; STABILITY; PROMOTER; GENES; ROLES; SLEEP;
D O I
10.1038/nn.3651
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The timing of daily circadian behavior can be highly variable among different individuals, and twin studies have suggested that about half of this variability is environmentally controlled. Similar plasticity can be seen in mice exposed to an altered lighting environment, for example, 22-h instead of 24-h, which stably alters the genetically determined period of circadian behavior for months. The mechanisms mediating these environmental influences are unknown. We found that transient exposure of mice to such lighting stably altered global transcription in the suprachiasmatic nucleus (SCN) of the hypothalamus (the master clock tissue regulating circadian behavior in mammals). In parallel, genome-wide methylation profiling revealed global alterations in promoter DNA methylation in the SCN that correlated with these changes. Behavioral, transcriptional and DNA methylation changes were reversible after prolonged re-entrainment to 24-h d. Notably, infusion of a methyltransferase inhibitor to the SCN suppressed period changes. We conclude that the SCN utilizes DNA methylation as a mechanism to drive circadian clock plasticity.
引用
收藏
页码:377 / 382
页数:6
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