Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.


Originally published in Science Express on 19 March 2009
Science 1 May 2009:
Vol. 324. no. 5927, pp. 651 - 654
DOI: 10.1126/science.1171641

Reports

Circadian Clock Feedback Cycle Through NAMPT-Mediated NAD+ Biosynthesis

Kathryn Moynihan Ramsey,1,2,3,* Jun Yoshino,6,* Cynthia S. Brace,6,* Dana Abrassart,1,2 Yumiko Kobayashi,1,2,3 Biliana Marcheva,1,2 Hee-Kyung Hong,2 Jason L. Chong,2 Ethan D. Buhr,2 Choogon Lee,4 Joseph S. Takahashi,2,5 Shin-ichiro Imai,6,{dagger} Joseph Bass1,2,3,{dagger}

The circadian clock is encoded by a transcription-translation feedback loop that synchronizes behavior and metabolism with the light-dark cycle. Here we report that both the rate-limiting enzyme in mammalian nicotinamide adenine dinucleotide (NAD+) biosynthesis, nicotinamide phosphoribosyltransferase (NAMPT), and levels of NAD+ display circadian oscillations that are regulated by the core clock machinery in mice. Inhibition of NAMPT promotes oscillation of the clock gene Per2 by releasing CLOCK:BMAL1 from suppression by SIRT1. In turn, the circadian transcription factor CLOCK binds to and up-regulates Nampt, thus completing a feedback loop involving NAMPT/NAD+ and SIRT1/CLOCK:BMAL1.

1 Department of Medicine, Northwestern University Feinberg School of Medicine, 2200 Campus Drive, Evanston, IL 60208–3500, USA.
2 Department of Neurobiology and Physiology, Northwestern University Feinberg School of Medicine, 2200 Campus Drive, Evanston, IL 60208–3500, USA.
3 NorthShore University Health System Research Institute and Department of Medicine, Evanston, IL 60201, USA.
4 Department of Biomedical Sciences, College of Medicine, Florida State University, Tallahassee, FL 32306, USA.
5 Howard Hughes Medical Institute, Northwestern University, Evanston, IL 60208, USA.
6 Department of Developmental Biology, Washington University School of Medicine, St. Louis, MO 63110, USA.

* These authors contributed equally to this work.

{dagger} To whom correspondence should be addressed. E-mail: imaishin{at}wustl.edu (S.I.); j-bass{at}northwestern.edu (J.B.)

Read the Full Text



THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Clock genes and metabolic disease.
B. Marcheva, K. M. Ramsey, A. Affinati, and J. Bass (2009)
J Appl Physiol 107, 1638-1646
   Abstract »    Full Text »    PDF »
Working around the clock: circadian rhythms and skeletal muscle.
X. Zhang, T. J. Dube, and K. A. Esser (2009)
J Appl Physiol 107, 1647-1654
   Abstract »    Full Text »    PDF »
Response to Comment on "The Arabidopsis Circadian Clock Incorporates a cADPR-Based Feedback Loop".
A. N. Dodd, M. J. Gardner, C. T. Hotta, K. E. Hubbard, N. Dalchau, F. C. Robertson, J. Love, D. Sanders, and A. A. R. Webb (2009)
Science 326, 230
   Abstract »    Full Text »    PDF »
SIRT1 controls circadian clock circuitry and promotes cell survival: a connection with age-related neoplasms.
B. Jung-Hynes and N. Ahmad (2009)
FASEB J 23, 2803-2809
   Abstract »    Full Text »    PDF »
Enzymes in the NAD+ Salvage Pathway Regulate SIRT1 Activity at Target Gene Promoters.
T. Zhang, J. G. Berrocal, K. M. Frizzell, M. J. Gamble, M. E. DuMond, R. Krishnakumar, T. Yang, A. A. Sauve, and W. L. Kraus (2009)
J. Biol. Chem. 284, 20408-20417
   Abstract »    Full Text »    PDF »
A Circadian Loop asSIRTs Itself.
H. Wijnen (2009)
Science 324, 598-599
   Abstract »    Full Text »    PDF »



To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)