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Diet-Induced Circadian Enhancer Remodeling Synchronizes Opposing Hepatic Lipid Metabolic Processes
Author(s) -
Dongyin Guan,
Ying Xiong,
Patrícia Cristine Borck,
Cholsoon Jang,
PaschalisThomas Doulias,
Romeo Papazyan,
Bin Fang,
Chunjie Jiang,
Yuxiang Zhang,
Erika R. Briggs,
Wenxiang Hu,
David J. Steger,
Harry Ischiropoulos,
Joshua D. Rabinowitz,
Mitchell A. Lazar
Publication year - 2018
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2018.06.031
Subject(s) - circadian rhythm , biology , overnutrition , endocrinology , medicine , circadian clock , lipogenesis , sterol regulatory element binding protein , lipid metabolism , peroxisome , endogeny , activator (genetics) , peroxisome proliferator activated receptor , microbiology and biotechnology , biochemistry , receptor , cholesterol , obesity , sterol
Overnutrition disrupts circadian metabolic rhythms by mechanisms that are not well understood. Here, we show that diet-induced obesity (DIO) causes massive remodeling of circadian enhancer activity in mouse liver, triggering synchronous high-amplitude circadian rhythms of both fatty acid (FA) synthesis and oxidation. SREBP expression was rhythmically induced by DIO, leading to circadian FA synthesis and, surprisingly, FA oxidation (FAO). DIO similarly caused a high-amplitude circadian rhythm of PPARα, which was also required for FAO. Provision of a pharmacological activator of PPARα abrogated the requirement of SREBP for FAO (but not FA synthesis), suggesting that SREBP indirectly controls FAO via production of endogenous PPARα ligands. The high-amplitude rhythm of PPARα imparted time-of-day-dependent responsiveness to lipid-lowering drugs. Thus, acquisition of rhythmicity for non-core clock components PPARα and SREBP1 remodels metabolic gene transcription in response to overnutrition and enables a chronopharmacological approach to metabolic disorders.

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