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The sleep-wake distribution contributes to the peripheral rhythms in PERIOD-2
In the mouse, Period-2 (Per2) expression in tissues peripheral to the suprachiasmatic nuclei (SCN) increases during sleep deprivation and at times of the day when animals are predominantly awake spontaneously, suggesting that the circadian sleep-wake distribution directly contributes to the daily rh...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798053/ https://www.ncbi.nlm.nih.gov/pubmed/34895464 http://dx.doi.org/10.7554/eLife.69773 |
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author | Hoekstra, Marieke MB Jan, Maxime Katsioudi, Georgia Emmenegger, Yann Franken, Paul |
author_facet | Hoekstra, Marieke MB Jan, Maxime Katsioudi, Georgia Emmenegger, Yann Franken, Paul |
author_sort | Hoekstra, Marieke MB |
collection | PubMed |
description | In the mouse, Period-2 (Per2) expression in tissues peripheral to the suprachiasmatic nuclei (SCN) increases during sleep deprivation and at times of the day when animals are predominantly awake spontaneously, suggesting that the circadian sleep-wake distribution directly contributes to the daily rhythms in Per2. We found support for this hypothesis by recording sleep-wake state alongside PER2 bioluminescence in freely behaving mice, demonstrating that PER2 bioluminescence increases during spontaneous waking and decreases during sleep. The temporary reinstatement of PER2-bioluminescence rhythmicity in behaviorally arrhythmic SCN-lesioned mice submitted to daily recurring sleep deprivations substantiates our hypothesis. Mathematical modeling revealed that PER2 dynamics can be described by a damped harmonic oscillator driven by two forces: a sleep-wake-dependent force and an SCN-independent circadian force. Our work underscores the notion that in peripheral tissues the clock gene circuitry integrates sleep-wake information and could thereby contribute to behavioral adaptability to respond to homeostatic requirements. |
format | Online Article Text |
id | pubmed-8798053 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-87980532022-01-31 The sleep-wake distribution contributes to the peripheral rhythms in PERIOD-2 Hoekstra, Marieke MB Jan, Maxime Katsioudi, Georgia Emmenegger, Yann Franken, Paul eLife Computational and Systems Biology In the mouse, Period-2 (Per2) expression in tissues peripheral to the suprachiasmatic nuclei (SCN) increases during sleep deprivation and at times of the day when animals are predominantly awake spontaneously, suggesting that the circadian sleep-wake distribution directly contributes to the daily rhythms in Per2. We found support for this hypothesis by recording sleep-wake state alongside PER2 bioluminescence in freely behaving mice, demonstrating that PER2 bioluminescence increases during spontaneous waking and decreases during sleep. The temporary reinstatement of PER2-bioluminescence rhythmicity in behaviorally arrhythmic SCN-lesioned mice submitted to daily recurring sleep deprivations substantiates our hypothesis. Mathematical modeling revealed that PER2 dynamics can be described by a damped harmonic oscillator driven by two forces: a sleep-wake-dependent force and an SCN-independent circadian force. Our work underscores the notion that in peripheral tissues the clock gene circuitry integrates sleep-wake information and could thereby contribute to behavioral adaptability to respond to homeostatic requirements. eLife Sciences Publications, Ltd 2021-12-13 /pmc/articles/PMC8798053/ /pubmed/34895464 http://dx.doi.org/10.7554/eLife.69773 Text en © 2021, Hoekstra et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Computational and Systems Biology Hoekstra, Marieke MB Jan, Maxime Katsioudi, Georgia Emmenegger, Yann Franken, Paul The sleep-wake distribution contributes to the peripheral rhythms in PERIOD-2 |
title | The sleep-wake distribution contributes to the peripheral rhythms in PERIOD-2 |
title_full | The sleep-wake distribution contributes to the peripheral rhythms in PERIOD-2 |
title_fullStr | The sleep-wake distribution contributes to the peripheral rhythms in PERIOD-2 |
title_full_unstemmed | The sleep-wake distribution contributes to the peripheral rhythms in PERIOD-2 |
title_short | The sleep-wake distribution contributes to the peripheral rhythms in PERIOD-2 |
title_sort | sleep-wake distribution contributes to the peripheral rhythms in period-2 |
topic | Computational and Systems Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798053/ https://www.ncbi.nlm.nih.gov/pubmed/34895464 http://dx.doi.org/10.7554/eLife.69773 |
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