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  Circadian control of oscillations in mitochondrial rate-limiting enzymes and nutrient utilization by PERIOD proteins

Neufeld-Cohen, A., Robles, M. S., Aviram, R., Manella, G., Adamovich, Y., Ladeuix, B., et al. (2016). Circadian control of oscillations in mitochondrial rate-limiting enzymes and nutrient utilization by PERIOD proteins. Proceedings of the National Academy of Sciences of the United States of America, 113(12), E1673-E1682. doi:10.1073/pnas.1519650113.

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 Creators:
Neufeld-Cohen, Adi1, Author
Robles, Maria S.2, Author           
Aviram, Rona1, Author
Manella, Gal1, Author
Adamovich, Yaarit1, Author
Ladeuix, Benjamin1, Author
Nir, Dana1, Author
Rousso-Noori, Liat1, Author
Kuperman, Yael1, Author
Golik, Marina1, Author
Mann, Matthias2, Author           
Asher, Gad1, Author
Affiliations:
1external, ou_persistent22              
2Mann, Matthias / Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565159              

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Free keywords: INTERNAL BODY TIME; HIGH-FAT DIET; GENE-EXPRESSION; ENERGY-EXPENDITURE; METABOLIC SYNDROME; SKELETAL-MUSCLE; CLOCK; LIVER; MICE; MOUSEcircadian rhythm; proteomics; metabolism; mitochondria; PERIOD proteins;
 Abstract: Mitochondria are major suppliers of cellular energy through nutrients oxidation. Little is known about the mechanisms that enable mitochondria to cope with changes in nutrient supply and energy demand that naturally occur throughout the day. To address this question, we applied MS-based quantitative proteomics on isolated mitochondria from mice killed throughout the day and identified extensive oscillations in the mitochondrial proteome. Remarkably, the majority of cycling mitochondrial proteins peaked during the early light phase. We found that rate-limiting mitochondrial enzymes that process lipids and carbohydrates accumulate in a diurnal manner and are dependent on the clock proteins PER1/2. In this conjuncture, we uncovered daily oscillations in mitochondrial respiration that peak during different times of the day in response to different nutrients. Notably, the diurnal regulation of mitochondrial respiration was blunted in mice lacking PER1/2 or on a high-fat diet. We propose that PERIOD proteins optimize mitochondrial metabolism to daily changes in energy supply/demand and thereby, serve as a rheostat for mitochondrial nutrient utilization.

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Language(s): eng - English
 Dates: 2016
 Publication Status: Issued
 Pages: 10
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: ISI: 000372488200013
DOI: 10.1073/pnas.1519650113
 Degree: -

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Title: Proceedings of the National Academy of Sciences of the United States of America
  Other : Proc. Acad. Sci. USA
  Other : Proc. Acad. Sci. U.S.A.
  Abbreviation : PNAS
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: Washington, D.C. : National Academy of Sciences
Pages: - Volume / Issue: 113 (12) Sequence Number: - Start / End Page: E1673 - E1682 Identifier: ISSN: 0027-8424
CoNE: https://pure.mpg.de/cone/journals/resource/954925427230