Circadian Clock NAD + Cycle Drives Mitochondrial Oxidative Metabolism in Mice

Author:

Peek Clara Bien12,Affinati Alison H.12,Ramsey Kathryn Moynihan12,Kuo Hsin-Yu34,Yu Wei5,Sena Laura A.67,Ilkayeva Olga8,Marcheva Biliana12,Kobayashi Yumiko12,Omura Chiaki12,Levine Daniel C.12,Bacsik David J.12,Gius David9,Newgard Christopher B.8,Goetzman Eric10,Chandel Navdeep S.67,Denu John M.5,Mrksich Milan34,Bass Joseph12

Affiliation:

1. Department of Medicine, Division of Endocrinology, Metabolism and Molecular Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.

2. Department of Neurobiology, Northwestern University, Evanston, IL 60208, USA.

3. Department of Chemistry, Northwestern University, Evanston, IL 60208, USA.

4. Howard Hughes Medical Institute, Northwestern University, Evanston, IL 60208, USA.

5. Department of Biomolecular Chemistry and Wisconsin Institute for Discovery, University of Wisconsin, Madison, WI 53715, USA.

6. Deparment of Medicine, Division of Pulmonary and Critical Care Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.

7. Department of Cell and Molecular Biology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.

8. Sarah W. Stedman Nutrition and Metabolism Center, Departments of Pharmacology and Cancer Biology and Medicine, Duke University Medical Center, Durham, NC 27705, USA.

9. Department of Radiation Oncology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.

10. Department of Pediatrics, Children’s Hospital of Pittsburgh, University of Pittsburgh School of Medicine, Pittsburgh, PA 15224, USA.

Abstract

Dinner Time! Biological clocks allow organisms to anticipate cycles of feeding, activity, and rest so that metabolic enzymes in mitochondria are ready when needed. Peek et al. ( 10.1126/science.1243417 , published online 19 September; see the Perspective by Rey and Reddy ) describe a mechanism by which the biochemical elements of the circadian clock are linked to such control of mitochondrial metabolism. The clock controls rhythmic transcription of the gene encoding the rate-limiting enzyme required for synthesis of nicotinamide adenine dinucleotide (NAD + ). The concentration of NAD + in mitochondria determines the activity of the deacetylase SIRT3, which then controls acetylation and activity of key metabolic enzymes. NAD+ also influences clock function, and thus appears to be a versatile point at which regulation of oxidative metabolism is coordinated with the daily cycles of energy consumption.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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