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p53 Regulates Period2 Expression and the Circadian Clock

The mechanistic interconnectivity between circadian regulation and the genotoxic stress response remains poorly understood. Here we show that the expression of Period 2 (Per2), a circadian regulator, is directly regulated by p53 binding to a response element in the Per2 promoter. This p53 response e...

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Autores principales: Miki, Takao, Matsumoto, Tomoko, Zhao, Zhaoyang, Lee, Cheng Chi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3798035/
https://www.ncbi.nlm.nih.gov/pubmed/24051492
http://dx.doi.org/10.1038/ncomms3444
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author Miki, Takao
Matsumoto, Tomoko
Zhao, Zhaoyang
Lee, Cheng Chi
author_facet Miki, Takao
Matsumoto, Tomoko
Zhao, Zhaoyang
Lee, Cheng Chi
author_sort Miki, Takao
collection PubMed
description The mechanistic interconnectivity between circadian regulation and the genotoxic stress response remains poorly understood. Here we show that the expression of Period 2 (Per2), a circadian regulator, is directly regulated by p53 binding to a response element in the Per2 promoter. This p53 response element is evolutionarily conserved and overlaps with the E-Box element critical for BMAL1/CLOCK binding and its transcriptional activation of Per2 expression. Our studies reveal that p53 blocks BMAL1/CLOCK binding to the Per2 promoter leading to repression of Per2 expression. In the suprachiasmatic nucleus (SCN), p53 expression and its binding to the Per2 promoter are under circadian control. Per2 expression in the SCN is altered by p53 deficiency or stabilization of p53 by Nutlin-3. Behaviorally, p53(−/−) mice have a shorter period length that lacks stability and they exhibit impaired photo-entrainment to a light pulse under a free-running state. Our studies demonstrate that p53 modulates mouse circadian behavior.
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spelling pubmed-37980352014-03-20 p53 Regulates Period2 Expression and the Circadian Clock Miki, Takao Matsumoto, Tomoko Zhao, Zhaoyang Lee, Cheng Chi Nat Commun Article The mechanistic interconnectivity between circadian regulation and the genotoxic stress response remains poorly understood. Here we show that the expression of Period 2 (Per2), a circadian regulator, is directly regulated by p53 binding to a response element in the Per2 promoter. This p53 response element is evolutionarily conserved and overlaps with the E-Box element critical for BMAL1/CLOCK binding and its transcriptional activation of Per2 expression. Our studies reveal that p53 blocks BMAL1/CLOCK binding to the Per2 promoter leading to repression of Per2 expression. In the suprachiasmatic nucleus (SCN), p53 expression and its binding to the Per2 promoter are under circadian control. Per2 expression in the SCN is altered by p53 deficiency or stabilization of p53 by Nutlin-3. Behaviorally, p53(−/−) mice have a shorter period length that lacks stability and they exhibit impaired photo-entrainment to a light pulse under a free-running state. Our studies demonstrate that p53 modulates mouse circadian behavior. 2013 /pmc/articles/PMC3798035/ /pubmed/24051492 http://dx.doi.org/10.1038/ncomms3444 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Miki, Takao
Matsumoto, Tomoko
Zhao, Zhaoyang
Lee, Cheng Chi
p53 Regulates Period2 Expression and the Circadian Clock
title p53 Regulates Period2 Expression and the Circadian Clock
title_full p53 Regulates Period2 Expression and the Circadian Clock
title_fullStr p53 Regulates Period2 Expression and the Circadian Clock
title_full_unstemmed p53 Regulates Period2 Expression and the Circadian Clock
title_short p53 Regulates Period2 Expression and the Circadian Clock
title_sort p53 regulates period2 expression and the circadian clock
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3798035/
https://www.ncbi.nlm.nih.gov/pubmed/24051492
http://dx.doi.org/10.1038/ncomms3444
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