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Rhythmic Food Intake Drives Rhythmic Gene Expression More Potently than the Hepatic Circadian Clock in Mice.
- Source :
-
Cell reports [Cell Rep] 2019 Apr 16; Vol. 27 (3), pp. 649-657.e5. - Publication Year :
- 2019
-
Abstract
- Every mammalian tissue exhibits daily rhythms in gene expression to control the activation of tissue-specific processes at the most appropriate time of the day. Much of this rhythmic expression is thought to be driven cell autonomously by molecular circadian clocks present throughout the body. By manipulating the daily rhythm of food intake in the mouse, we here show that more than 70% of the cycling mouse liver transcriptome loses rhythmicity under arrhythmic feeding. Remarkably, core clock genes are not among the 70% of genes losing rhythmic expression, and their expression continues to exhibit normal oscillations in arrhythmically fed mice. Manipulation of rhythmic food intake also alters the timing of key signaling and metabolic pathways without altering the hepatic clock oscillations. Our findings thus demonstrate that systemic signals driven by rhythmic food intake significantly contribute to driving rhythms in liver gene expression and metabolic functions independently of the cell-autonomous hepatic clock.<br /> (Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- ARNTL Transcription Factors deficiency
ARNTL Transcription Factors genetics
ARNTL Transcription Factors metabolism
Animals
Behavior, Animal
Blood Glucose analysis
Gene Expression Regulation
Insulin administration & dosage
Lipogenesis
Male
Metabolic Networks and Pathways genetics
Mice
Mice, Inbred C57BL
Mice, Knockout
Mitogen-Activated Protein Kinase 1 metabolism
Mitogen-Activated Protein Kinase 3 metabolism
TOR Serine-Threonine Kinases metabolism
Circadian Clocks genetics
Eating
Liver metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2211-1247
- Volume :
- 27
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Cell reports
- Publication Type :
- Academic Journal
- Accession number :
- 30995463
- Full Text :
- https://doi.org/10.1016/j.celrep.2019.03.064