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Emergence of Noise-Induced Oscillations in the Central Circadian Pacemaker
Bmal1 is an essential transcriptional activator within the mammalian circadian clock. We report here that the suprachiasmatic nucleus (SCN) of Bmal1-null mutant mice, unexpectedly, generates stochastic oscillations with periods that overlap the circadian range. Dissociated SCN neurons expressed fluc...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2953532/ https://www.ncbi.nlm.nih.gov/pubmed/20967239 http://dx.doi.org/10.1371/journal.pbio.1000513 |
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author | Ko, Caroline H. Yamada, Yujiro R. Welsh, David K. Buhr, Ethan D. Liu, Andrew C. Zhang, Eric E. Ralph, Martin R. Kay, Steve A. Forger, Daniel B. Takahashi, Joseph S. |
author_facet | Ko, Caroline H. Yamada, Yujiro R. Welsh, David K. Buhr, Ethan D. Liu, Andrew C. Zhang, Eric E. Ralph, Martin R. Kay, Steve A. Forger, Daniel B. Takahashi, Joseph S. |
author_sort | Ko, Caroline H. |
collection | PubMed |
description | Bmal1 is an essential transcriptional activator within the mammalian circadian clock. We report here that the suprachiasmatic nucleus (SCN) of Bmal1-null mutant mice, unexpectedly, generates stochastic oscillations with periods that overlap the circadian range. Dissociated SCN neurons expressed fluctuating levels of PER2 detected by bioluminescence imaging but could not generate circadian oscillations intrinsically. Inhibition of intercellular communication or cyclic-AMP signaling in SCN slices, which provide a positive feed-forward signal to drive the intracellular negative feedback loop, abolished the stochastic oscillations. Propagation of this feed-forward signal between SCN neurons then promotes quasi-circadian oscillations that arise as an emergent property of the SCN network. Experimental analysis and mathematical modeling argue that both intercellular coupling and molecular noise are required for the stochastic rhythms, providing a novel biological example of noise-induced oscillations. The emergence of stochastic circadian oscillations from the SCN network in the absence of cell-autonomous circadian oscillatory function highlights a previously unrecognized level of circadian organization. |
format | Text |
id | pubmed-2953532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-29535322010-10-21 Emergence of Noise-Induced Oscillations in the Central Circadian Pacemaker Ko, Caroline H. Yamada, Yujiro R. Welsh, David K. Buhr, Ethan D. Liu, Andrew C. Zhang, Eric E. Ralph, Martin R. Kay, Steve A. Forger, Daniel B. Takahashi, Joseph S. PLoS Biol Research Article Bmal1 is an essential transcriptional activator within the mammalian circadian clock. We report here that the suprachiasmatic nucleus (SCN) of Bmal1-null mutant mice, unexpectedly, generates stochastic oscillations with periods that overlap the circadian range. Dissociated SCN neurons expressed fluctuating levels of PER2 detected by bioluminescence imaging but could not generate circadian oscillations intrinsically. Inhibition of intercellular communication or cyclic-AMP signaling in SCN slices, which provide a positive feed-forward signal to drive the intracellular negative feedback loop, abolished the stochastic oscillations. Propagation of this feed-forward signal between SCN neurons then promotes quasi-circadian oscillations that arise as an emergent property of the SCN network. Experimental analysis and mathematical modeling argue that both intercellular coupling and molecular noise are required for the stochastic rhythms, providing a novel biological example of noise-induced oscillations. The emergence of stochastic circadian oscillations from the SCN network in the absence of cell-autonomous circadian oscillatory function highlights a previously unrecognized level of circadian organization. Public Library of Science 2010-10-12 /pmc/articles/PMC2953532/ /pubmed/20967239 http://dx.doi.org/10.1371/journal.pbio.1000513 Text en Ko et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Ko, Caroline H. Yamada, Yujiro R. Welsh, David K. Buhr, Ethan D. Liu, Andrew C. Zhang, Eric E. Ralph, Martin R. Kay, Steve A. Forger, Daniel B. Takahashi, Joseph S. Emergence of Noise-Induced Oscillations in the Central Circadian Pacemaker |
title | Emergence of Noise-Induced Oscillations in the Central Circadian Pacemaker |
title_full | Emergence of Noise-Induced Oscillations in the Central Circadian Pacemaker |
title_fullStr | Emergence of Noise-Induced Oscillations in the Central Circadian Pacemaker |
title_full_unstemmed | Emergence of Noise-Induced Oscillations in the Central Circadian Pacemaker |
title_short | Emergence of Noise-Induced Oscillations in the Central Circadian Pacemaker |
title_sort | emergence of noise-induced oscillations in the central circadian pacemaker |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2953532/ https://www.ncbi.nlm.nih.gov/pubmed/20967239 http://dx.doi.org/10.1371/journal.pbio.1000513 |
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