Abstract |
In mammals, 24 hours rhythms are organized as a biochemical network of molecular clocks that are operative in all tissues, with the master clock residing in the hypothalamic suprachiasmatic nucleus (SCN). The core pacemakers of these clocks consist of auto-regulatory transcriptional/post-transcriptional feedback loops. Several lines of evidence suggest the existence of a crosstalk between molecules that are responsible for the generation of circadian rhythms and molecules that control the cell cycle progression. In addition, highly specialized cell cycle checkpoints involved in DNA repair after damage seem also, at least in part, mediated by clock proteins. Recent studies have also highlighted a putative connection between clock protein dysfunction and cancer progression. This review discusses the intimate relation that exists between cell cycle progression and components of the circadian machinery.
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Authors | Laurence Borgs, Pierre Beukelaers, Renaud Vandenbosch, Shibeshih Belachew, Laurent Nguyen, Brigitte Malgrange |
Journal | Cell cycle (Georgetown, Tex.)
(Cell Cycle)
Vol. 8
Issue 6
Pg. 832-7
(Mar 15 2009)
ISSN: 1551-4005 [Electronic] United States |
PMID | 19221497
(Publication Type: Journal Article, Review)
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Chemical References |
- Cell Cycle Proteins
- Trans-Activators
- Transcription Factors
- CLOCK Proteins
- CLOCK protein, human
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Topics |
- Animals
- Biological Clocks
(genetics, physiology)
- CLOCK Proteins
- Cell Cycle
(genetics, physiology)
- Cell Cycle Proteins
(genetics, metabolism)
- Circadian Rhythm
(genetics, physiology)
- DNA Damage
(genetics, physiology)
- Humans
- Signal Transduction
(genetics, physiology)
- Trans-Activators
(genetics, metabolism)
- Transcription Factors
(genetics, metabolism)
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