Center for Epigenetics and Metabolism, Department of Biological Chemistry, University of California, Irvine, Irvine, CA 92697, USA.
Institute for Genomics and Bioinformatics, School of Information and Computer Sciences, University of California, Irvine, Irvine, CA 92697, USA.
Cell. 2013 Dec 19;155(7):1464-78. doi: 10.1016/j.cell.2013.11.034.
Circadian rhythms and cellular metabolism are intimately linked. Here, we reveal that a high-fat diet (HFD) generates a profound reorganization of specific metabolic pathways, leading to widespread remodeling of the liver clock. Strikingly, in addition to disrupting the normal circadian cycle, HFD causes an unexpectedly large-scale genesis of de novo oscillating transcripts, resulting in reorganization of the coordinated oscillations between coherent transcripts and metabolites. The mechanisms underlying this reprogramming involve both the impairment of CLOCK:BMAL1 chromatin recruitment and a pronounced cyclic activation of surrogate pathways through the transcriptional regulator PPARγ. Finally, we demonstrate that it is specifically the nutritional challenge, and not the development of obesity, that causes the reprogramming of the clock and that the effects of the diet on the clock are reversible.
昼夜节律和细胞代谢密切相关。在这里,我们揭示了高脂肪饮食(HFD)会对特定代谢途径进行深刻的重新组织,从而导致肝脏时钟的广泛重塑。引人注目的是,除了扰乱正常的昼夜节律周期外,HFD 还会导致出乎意料的大规模新出现的振荡转录本的产生,从而导致相干转录本和代谢物之间协调振荡的重新组织。这种重编程的机制既涉及 CLOCK:BMAL1 染色质募集的损害,也涉及通过转录调节因子 PPARγ 对替代途径的明显周期性激活。最后,我们证明正是营养挑战,而不是肥胖的发展,导致了时钟的重新编程,而且饮食对时钟的影响是可逆的。