4.8 Article

Peroxiredoxins are conserved markers of circadian rhythms

期刊

NATURE
卷 485, 期 7399, 页码 459-U65

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/nature11088

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资金

  1. Wellcome Trust [083643/Z/07/Z, 093734/Z/10/Z]
  2. European Research Council (ERC) [281348]
  3. EMBO
  4. Medical Research Council Centre for Obesity and Related metabolic Disorders (MRC CORD)
  5. National Institute for Health Research (NIHR) Cambridge Biomedical Research Centre
  6. European Commission [018741]
  7. Biotechnology and Biological Sciences Research Council (BBSRC) [BB/C006941/1]
  8. Engineering and Physical Sciences Research Council (EPSRC) [BB/D019621]
  9. ENIGMA
  10. US Department of Energy [DE-AC02-05CH11231]
  11. National Institutes of Health (NIH) [P50GM076547, R01GM088595, R01GM067152, R21HL102492]
  12. Netherlands Organisation for Scientific Research (NWO)
  13. Dutch Science Foundation VICI
  14. University of Groningen
  15. Wellcome Trust [083643/Z/07/Z] Funding Source: Wellcome Trust
  16. Biotechnology and Biological Sciences Research Council [BB/D019621/1, BB/C006941/1] Funding Source: researchfish
  17. Medical Research Council [MC_U105170643, MC_UP_1201/4, G0600717B] Funding Source: researchfish
  18. BBSRC [BB/D019621/1] Funding Source: UKRI
  19. MRC [MC_UP_1201/4, MC_U105170643] Funding Source: UKRI

向作者/读者索取更多资源

Cellular life emerged similar to 3.7 billion years ago. With scant exception, terrestrial organisms have evolved under predictable daily cycles owing to the Earth's rotation. The advantage conferred on organisms that anticipate such environmental cycles has driven the evolution of endogenous circadian rhythms that tune internal physiology to external conditions. The molecular phylogeny of mechanisms driving these rhythms has been difficult to dissect because identified clock genes and proteins are not conserved across the domains of life: Bacteria, Archaea and Eukaryota. Here we show that oxidation-reduction cycles of peroxiredoxin proteins constitute a universal marker for circadian rhythms in all domains of life, by characterizing their oscillations in a variety of model organisms. Furthermore, we explore the interconnectivity between these metabolic cycles and transcription-translation feedback loops of the clockwork in each system. Our results suggest an intimate co-evolution of cellular timekeeping with redox homeostatic mechanisms after the Great Oxidation Event similar to 2.5 billion years ago.

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