Cargando…
A Novel Mechanism Controlling Resetting Speed of the Circadian Clock to Environmental Stimuli
Many aspects of mammalian physiology are driven through the coordinated action of internal circadian clocks. Clock speed (period) and phase (temporal alignment) are fundamental to an organism’s ability to synchronize with its environment. In humans, lifestyles that disturb these clocks, such as shif...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3988889/ https://www.ncbi.nlm.nih.gov/pubmed/24656826 http://dx.doi.org/10.1016/j.cub.2014.02.027 |
_version_ | 1782312084075184128 |
---|---|
author | Pilorz, Violetta Cunningham, Peter S. Jackson, Anthony West, Alexander C. Wager, Travis T. Loudon, Andrew S.I. Bechtold, David A. |
author_facet | Pilorz, Violetta Cunningham, Peter S. Jackson, Anthony West, Alexander C. Wager, Travis T. Loudon, Andrew S.I. Bechtold, David A. |
author_sort | Pilorz, Violetta |
collection | PubMed |
description | Many aspects of mammalian physiology are driven through the coordinated action of internal circadian clocks. Clock speed (period) and phase (temporal alignment) are fundamental to an organism’s ability to synchronize with its environment. In humans, lifestyles that disturb these clocks, such as shift work, increase the incidence of diseases such as cancer and diabetes. Casein kinases 1δ and ε are closely related clock components implicated in period determination. However, CK1δ is so dominant in this regard that it remains unclear what function CK1ε normally serves. Here, we reveal that CK1ε dictates how rapidly the clock is reset by environmental stimuli. Genetic disruption of CK1ε in mice enhances phase resetting of behavioral rhythms to acute light pulses and shifts in light cycle. This impact of CK1ε targeting is recapitulated in isolated brain suprachiasmatic nucleus and peripheral (lung) clocks during NMDA- or temperature-induced phase shift in association with altered PERIOD (PER) protein dynamics. Importantly, accelerated re-entrainment of the circadian system in vivo and in vitro can be achieved in wild-type animals through pharmacological inhibition of CK1ε. These studies therefore reveal a role for CK1ε in stabilizing the circadian clock against phase shift and highlight it as a novel target for minimizing physiological disturbance in shift workers. |
format | Online Article Text |
id | pubmed-3988889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39888892014-04-17 A Novel Mechanism Controlling Resetting Speed of the Circadian Clock to Environmental Stimuli Pilorz, Violetta Cunningham, Peter S. Jackson, Anthony West, Alexander C. Wager, Travis T. Loudon, Andrew S.I. Bechtold, David A. Curr Biol Report Many aspects of mammalian physiology are driven through the coordinated action of internal circadian clocks. Clock speed (period) and phase (temporal alignment) are fundamental to an organism’s ability to synchronize with its environment. In humans, lifestyles that disturb these clocks, such as shift work, increase the incidence of diseases such as cancer and diabetes. Casein kinases 1δ and ε are closely related clock components implicated in period determination. However, CK1δ is so dominant in this regard that it remains unclear what function CK1ε normally serves. Here, we reveal that CK1ε dictates how rapidly the clock is reset by environmental stimuli. Genetic disruption of CK1ε in mice enhances phase resetting of behavioral rhythms to acute light pulses and shifts in light cycle. This impact of CK1ε targeting is recapitulated in isolated brain suprachiasmatic nucleus and peripheral (lung) clocks during NMDA- or temperature-induced phase shift in association with altered PERIOD (PER) protein dynamics. Importantly, accelerated re-entrainment of the circadian system in vivo and in vitro can be achieved in wild-type animals through pharmacological inhibition of CK1ε. These studies therefore reveal a role for CK1ε in stabilizing the circadian clock against phase shift and highlight it as a novel target for minimizing physiological disturbance in shift workers. Cell Press 2014-03-31 /pmc/articles/PMC3988889/ /pubmed/24656826 http://dx.doi.org/10.1016/j.cub.2014.02.027 Text en © 2014 The Authors http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Report Pilorz, Violetta Cunningham, Peter S. Jackson, Anthony West, Alexander C. Wager, Travis T. Loudon, Andrew S.I. Bechtold, David A. A Novel Mechanism Controlling Resetting Speed of the Circadian Clock to Environmental Stimuli |
title | A Novel Mechanism Controlling Resetting Speed of the Circadian Clock to Environmental Stimuli |
title_full | A Novel Mechanism Controlling Resetting Speed of the Circadian Clock to Environmental Stimuli |
title_fullStr | A Novel Mechanism Controlling Resetting Speed of the Circadian Clock to Environmental Stimuli |
title_full_unstemmed | A Novel Mechanism Controlling Resetting Speed of the Circadian Clock to Environmental Stimuli |
title_short | A Novel Mechanism Controlling Resetting Speed of the Circadian Clock to Environmental Stimuli |
title_sort | novel mechanism controlling resetting speed of the circadian clock to environmental stimuli |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3988889/ https://www.ncbi.nlm.nih.gov/pubmed/24656826 http://dx.doi.org/10.1016/j.cub.2014.02.027 |
work_keys_str_mv | AT pilorzvioletta anovelmechanismcontrollingresettingspeedofthecircadianclocktoenvironmentalstimuli AT cunninghampeters anovelmechanismcontrollingresettingspeedofthecircadianclocktoenvironmentalstimuli AT jacksonanthony anovelmechanismcontrollingresettingspeedofthecircadianclocktoenvironmentalstimuli AT westalexanderc anovelmechanismcontrollingresettingspeedofthecircadianclocktoenvironmentalstimuli AT wagertravist anovelmechanismcontrollingresettingspeedofthecircadianclocktoenvironmentalstimuli AT loudonandrewsi anovelmechanismcontrollingresettingspeedofthecircadianclocktoenvironmentalstimuli AT bechtolddavida anovelmechanismcontrollingresettingspeedofthecircadianclocktoenvironmentalstimuli AT pilorzvioletta novelmechanismcontrollingresettingspeedofthecircadianclocktoenvironmentalstimuli AT cunninghampeters novelmechanismcontrollingresettingspeedofthecircadianclocktoenvironmentalstimuli AT jacksonanthony novelmechanismcontrollingresettingspeedofthecircadianclocktoenvironmentalstimuli AT westalexanderc novelmechanismcontrollingresettingspeedofthecircadianclocktoenvironmentalstimuli AT wagertravist novelmechanismcontrollingresettingspeedofthecircadianclocktoenvironmentalstimuli AT loudonandrewsi novelmechanismcontrollingresettingspeedofthecircadianclocktoenvironmentalstimuli AT bechtolddavida novelmechanismcontrollingresettingspeedofthecircadianclocktoenvironmentalstimuli |