4.8 Article

The Pentose Phosphate Pathway Regulates the Circadian Clock

Journal

CELL METABOLISM
Volume 24, Issue 3, Pages 462-473

Publisher

CELL PRESS
DOI: 10.1016/j.cmet.2016.07.024

Keywords

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Funding

  1. Wellcome Trust [100333/Z/12/Z, 100574/Z/12/Z, 093734/Z/10/Z]
  2. European Research Council (ERC) [281348]
  3. EMBO
  4. Lister Institute of Preventive Medicine
  5. Medical Research Council [MRC_MC_UU_12012/5, MC_UP_1201/4]
  6. SNSF
  7. Medical Research Council [MC_UP_1201/4, MC_UU_12012/5/B, MC_UU_12012/5] Funding Source: researchfish
  8. The Francis Crick Institute [10534] Funding Source: researchfish
  9. MRC [MC_UP_1201/4, MC_UU_12012/5] Funding Source: UKRI
  10. Wellcome Trust [100333/Z/12/Z] Funding Source: Wellcome Trust

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The circadian clock is a ubiquitous timekeeping system that organizes the behavior and physiology of organisms over the day and night. Current models rely on transcriptional networks that coordinate circadian gene expression of thousands of transcripts. However, recent studies have uncovered phylogenetically conserved redox rhythms that can occur independently of transcriptional cycles. Here we identify the pentose phosphate pathway (PPP), a critical source of the redox cofactor NADPH, as an important regulator of redox and transcriptional oscillations. Our results show that genetic and pharmacological inhibition of the PPP prolongs the period of circadian rhythms in human cells, mouse tissues, and fruit flies. These metabolic manipulations also cause a remodeling of circadian gene expression programs that involves the circadian transcription factors BMAL1 and CLOCK, and the redox-sensitive transcription factor NRF2. Thus, the PPP regulates circadian rhythms via NADPH metabolism, suggesting a pivotal role for NADPH availability in circadian timekeeping.

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