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PMID: 21641546 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

The circadian clock interacts with metabolic physiology to influence reproductive fitness.

Cell metabolism ·Vol. 13 ·No. 6 ·2011-06-08 ·Pages 639-54

Xu K, DiAngelo JR, Hughes ME, Hogenesch JB, Sehgal A

Abstract

Circadian rhythms are regulated by a synchronized system of central and peripheral clocks. Here, we show that a clock in the Drosophila fat body drives rhythmic expression of genes involved in metabolism, detoxification, the immune response, and steroid hormone regulation. Some of these genes cycle even when the fat body clock is disrupted, indicating that they are regulated by exogenous factors. Food is an important stimulus, as limiting food availability to a 6 hr interval each day drives rhythmic expression of genes in the fat body. Restricting food to a time of day when consumption is typically low desynchronizes internal rhythms because it alters the phase of rhythmic gene expression in the fat body without affecting the brain clock. Flies maintained on this paradigm produce fewer eggs than those restricted to food at the normal time. These data suggest that desynchrony of endogenous rhythms, caused by aberrant feeding patterns, affects reproductive fitness.

MeSH Terms
Adaptive Immunity/genetics Animals Biotransformation/genetics Brain/metabolism CLOCK Proteins/genetics,metabolism Carbohydrate Metabolism/genetics Circadian Clocks/genetics Drosophila Proteins/genetics,metabolism Drosophila melanogaster/physiology Fat Body/physiology Female Food Deprivation Gene Expression Profiling Genes, Insect Genetic Fitness Lipid Metabolism/genetics Male Oligonucleotide Array Sequence Analysis Ovum/metabolism Reproduction/genetics Signal Transduction
Chemicals
Clk protein, Drosophila Drosophila Proteins CLOCK Proteins
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Xu Kanyan
Department of Neuroscience, Howard Hughes Medical Institute, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.
DiAngelo Justin R
Hughes Michael E
Hogenesch John B
Sehgal Amita
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Article Info
Journal
Cell metabolism
Abbr.
Cell Metab
ISSN
1932-7420
Published
2011-06-08
Pages
639-54
Language
English
Region
United States
NLM ID
101233170
PMCID
PMC3152999
Subset
IM
Grants
NINDS NIH HHS · R56 NS048471 · United States
NIA NIH HHS · P01 AG017628-08 · United States
NHLBI NIH HHS · 1R01HL097800 · United States
Howard Hughes Medical Institute · United States
NINDS NIH HHS · 1R56NS048471 · United States
NINDS NIH HHS · R01 NS054794 · United States
NHLBI NIH HHS · R01 HL097800 · United States
NIMH NIH HHS · P50 MH074924 · United States
NIA NIH HHS · P01 AG017628-09 · United States
NIA NIH HHS · P01 AG017628 · United States
NIA NIH HHS · T32 AG000255 · United States
NIA NIH HHS · T32-AG000255 · United States
NINDS NIH HHS · 1R01NS054794 · United States
NINDS NIH HHS · R56 NS048471-06 · United States
NINDS NIH HHS · R01 NS048471 · United States
NINDS NIH HHS · 1R01NS048471 · United States
NINDS NIH HHS · R01 NS048471-05 · United States
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