Cellular Timekeeping: It’s Redox o’Clock

  1. Akhilesh B. Reddy1,3
  1. 1The Francis Crick Institute, London NW1 1AT, United Kingdom
  2. 2Yonsei University College of Medicine, Seodaemun-gu, Seoul 120-752, Korea
  3. 3UCL Institute of Neurology, London WC1N 3BG, United Kingdom
  1. Correspondence: areddy{at}cantab.net

Abstract

Mounting evidence in recent years supports the extensive interaction between the circadian and redox systems. The existence of such a relationship is not surprising because most organisms, be they diurnal or nocturnal, display daily oscillations in energy intake, locomotor activity, and exposure to exogenous and internally generated oxidants. The transcriptional clock controls the levels of many antioxidant proteins and redox-active cofactors, and, conversely, the cellular redox poise has been shown to feed back to the transcriptional oscillator via redox-sensitive transcription factors and enzymes. However, the circadian cycles in the S-sulfinylation of the peroxiredoxin (PRDX) proteins constituted the first example of an autonomous circadian redox oscillation, which occurred independently of the transcriptional clock. Importantly, the high phylogenetic conservation of these rhythms suggests that they might predate the evolution of the transcriptional oscillator, and therefore could be a part of a primordial circadian redox/metabolic oscillator. This discovery forced the reappraisal of the dogmatic transcription-centered view of the clockwork and opened a new avenue of research. Indeed, the investigation into the links between the circadian and redox systems is still in its infancy, and many important questions remain to be addressed.



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      1. Cold Spring Harb. Perspect. Biol. 10: a027698 Copyright © 2018 Cold Spring Harbor Laboratory Press; all rights reserved

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