A novel protein, CHRONO, functions as a core component of the mammalian circadian clock.

Circadian rhythms are controlled by a system of negative and positive genetic feedback loops composed of clock genes. Although many genes have been implicated in these feedback loops, it is unclear whether our current list of clock genes is exhaustive. We have recently identified Chrono as a robustl...

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Autores principales: Akihiro Goriki, Fumiyuki Hatanaka, Jihwan Myung, Jae Kyoung Kim, Takashi Yoritaka, Shintaro Tanoue, Takaya Abe, Hiroshi Kiyonari, Katsumi Fujimoto, Yukio Kato, Takashi Todo, Akio Matsubara, Daniel Forger, Toru Takumi
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Publicado: Public Library of Science (PLoS) 2014
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Acceso en línea:https://doaj.org/article/3fbbaabf77d64dd197bfbf0eb6df3720
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spelling oai:doaj.org-article:3fbbaabf77d64dd197bfbf0eb6df37202021-11-18T05:37:30ZA novel protein, CHRONO, functions as a core component of the mammalian circadian clock.1544-91731545-788510.1371/journal.pbio.1001839https://doaj.org/article/3fbbaabf77d64dd197bfbf0eb6df37202014-04-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24736997/?tool=EBIhttps://doaj.org/toc/1544-9173https://doaj.org/toc/1545-7885Circadian rhythms are controlled by a system of negative and positive genetic feedback loops composed of clock genes. Although many genes have been implicated in these feedback loops, it is unclear whether our current list of clock genes is exhaustive. We have recently identified Chrono as a robustly cycling transcript through genome-wide profiling of BMAL1 binding on the E-box. Here, we explore the role of Chrono in cellular timekeeping. Remarkably, endogenous CHRONO occupancy around E-boxes shows a circadian oscillation antiphasic to BMAL1. Overexpression of Chrono leads to suppression of BMAL1-CLOCK activity in a histone deacetylase (HDAC) -dependent manner. In vivo loss-of-function studies of Chrono including Avp neuron-specific knockout (KO) mice display a longer circadian period of locomotor activity. Chrono KO also alters the expression of core clock genes and impairs the response of the circadian clock to stress. CHRONO forms a complex with the glucocorticoid receptor and mediates glucocorticoid response. Our comprehensive study spotlights a previously unrecognized clock component of an unsuspected negative circadian feedback loop that is independent of another negative regulator, Cry2, and that integrates behavioral stress and epigenetic control for efficient metabolic integration of the clock.Akihiro GorikiFumiyuki HatanakaJihwan MyungJae Kyoung KimTakashi YoritakaShintaro TanoueTakaya AbeHiroshi KiyonariKatsumi FujimotoYukio KatoTakashi TodoAkio MatsubaraDaniel ForgerToru TakumiPublic Library of Science (PLoS)articleBiology (General)QH301-705.5ENPLoS Biology, Vol 12, Iss 4, p e1001839 (2014)
institution DOAJ
collection DOAJ
language EN
topic Biology (General)
QH301-705.5
spellingShingle Biology (General)
QH301-705.5
Akihiro Goriki
Fumiyuki Hatanaka
Jihwan Myung
Jae Kyoung Kim
Takashi Yoritaka
Shintaro Tanoue
Takaya Abe
Hiroshi Kiyonari
Katsumi Fujimoto
Yukio Kato
Takashi Todo
Akio Matsubara
Daniel Forger
Toru Takumi
A novel protein, CHRONO, functions as a core component of the mammalian circadian clock.
description Circadian rhythms are controlled by a system of negative and positive genetic feedback loops composed of clock genes. Although many genes have been implicated in these feedback loops, it is unclear whether our current list of clock genes is exhaustive. We have recently identified Chrono as a robustly cycling transcript through genome-wide profiling of BMAL1 binding on the E-box. Here, we explore the role of Chrono in cellular timekeeping. Remarkably, endogenous CHRONO occupancy around E-boxes shows a circadian oscillation antiphasic to BMAL1. Overexpression of Chrono leads to suppression of BMAL1-CLOCK activity in a histone deacetylase (HDAC) -dependent manner. In vivo loss-of-function studies of Chrono including Avp neuron-specific knockout (KO) mice display a longer circadian period of locomotor activity. Chrono KO also alters the expression of core clock genes and impairs the response of the circadian clock to stress. CHRONO forms a complex with the glucocorticoid receptor and mediates glucocorticoid response. Our comprehensive study spotlights a previously unrecognized clock component of an unsuspected negative circadian feedback loop that is independent of another negative regulator, Cry2, and that integrates behavioral stress and epigenetic control for efficient metabolic integration of the clock.
format article
author Akihiro Goriki
Fumiyuki Hatanaka
Jihwan Myung
Jae Kyoung Kim
Takashi Yoritaka
Shintaro Tanoue
Takaya Abe
Hiroshi Kiyonari
Katsumi Fujimoto
Yukio Kato
Takashi Todo
Akio Matsubara
Daniel Forger
Toru Takumi
author_facet Akihiro Goriki
Fumiyuki Hatanaka
Jihwan Myung
Jae Kyoung Kim
Takashi Yoritaka
Shintaro Tanoue
Takaya Abe
Hiroshi Kiyonari
Katsumi Fujimoto
Yukio Kato
Takashi Todo
Akio Matsubara
Daniel Forger
Toru Takumi
author_sort Akihiro Goriki
title A novel protein, CHRONO, functions as a core component of the mammalian circadian clock.
title_short A novel protein, CHRONO, functions as a core component of the mammalian circadian clock.
title_full A novel protein, CHRONO, functions as a core component of the mammalian circadian clock.
title_fullStr A novel protein, CHRONO, functions as a core component of the mammalian circadian clock.
title_full_unstemmed A novel protein, CHRONO, functions as a core component of the mammalian circadian clock.
title_sort novel protein, chrono, functions as a core component of the mammalian circadian clock.
publisher Public Library of Science (PLoS)
publishDate 2014
url https://doaj.org/article/3fbbaabf77d64dd197bfbf0eb6df3720
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