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Transition of phase response properties and singularity in the circadian limit cycle of cultured cells

The circadian system has been regarded as a limit cycle oscillator constructed by the integrated interaction of clock genes and proteins. Here, we investigated a mammalian circadian oscillation geometrically before and after a perturbation. We detected the singular point and transition from a type 1...

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Autores principales: Koinuma, Satoshi, Kori, Hiroshi, Tokuda, Isao T., Yagita, Kazuhiro, Shigeyoshi, Yasufumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5513448/
https://www.ncbi.nlm.nih.gov/pubmed/28715496
http://dx.doi.org/10.1371/journal.pone.0181223
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author Koinuma, Satoshi
Kori, Hiroshi
Tokuda, Isao T.
Yagita, Kazuhiro
Shigeyoshi, Yasufumi
author_facet Koinuma, Satoshi
Kori, Hiroshi
Tokuda, Isao T.
Yagita, Kazuhiro
Shigeyoshi, Yasufumi
author_sort Koinuma, Satoshi
collection PubMed
description The circadian system has been regarded as a limit cycle oscillator constructed by the integrated interaction of clock genes and proteins. Here, we investigated a mammalian circadian oscillation geometrically before and after a perturbation. We detected the singular point and transition from a type 1 to type 0 phase response curve (PRC) and determined the embedding dimension to show how many variables are needed to describe the limit cycle oscillation and relaxation process after a perturbation. As a perturbation, forskolin (FK) was administered to Rat-1 cells expressing the Per2::luc gene. By broadly and finely changing the phase and strength of the perturbation, we detected the transition of the PRC from type 1 to type 0 and a possible singular transition point, the property of which agreed quite well with our numerical simulation of the noisy Goodwin model, a simple yet canonical model for the transcription-translation feedback loop of the core clock genes. Furthermore, we estimated the embedding dimension of the limit cycle before and after the perturbation. The trajectory of the limit cycle was embedded in two dimensions but with the perturbation of the state point moved out of the trajectory, the relaxation process was generally embedded in higher dimensions. The average number of embedding dimensions at each dose of FK increased as the FK dose increased but most of the relaxation process was generally embedded within four dimensions. These findings support the existence of a circadian limit cycle oscillator in mammalian cells and suggest that a small number of variables determine the relaxation process after a perturbation.
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spelling pubmed-55134482017-08-07 Transition of phase response properties and singularity in the circadian limit cycle of cultured cells Koinuma, Satoshi Kori, Hiroshi Tokuda, Isao T. Yagita, Kazuhiro Shigeyoshi, Yasufumi PLoS One Research Article The circadian system has been regarded as a limit cycle oscillator constructed by the integrated interaction of clock genes and proteins. Here, we investigated a mammalian circadian oscillation geometrically before and after a perturbation. We detected the singular point and transition from a type 1 to type 0 phase response curve (PRC) and determined the embedding dimension to show how many variables are needed to describe the limit cycle oscillation and relaxation process after a perturbation. As a perturbation, forskolin (FK) was administered to Rat-1 cells expressing the Per2::luc gene. By broadly and finely changing the phase and strength of the perturbation, we detected the transition of the PRC from type 1 to type 0 and a possible singular transition point, the property of which agreed quite well with our numerical simulation of the noisy Goodwin model, a simple yet canonical model for the transcription-translation feedback loop of the core clock genes. Furthermore, we estimated the embedding dimension of the limit cycle before and after the perturbation. The trajectory of the limit cycle was embedded in two dimensions but with the perturbation of the state point moved out of the trajectory, the relaxation process was generally embedded in higher dimensions. The average number of embedding dimensions at each dose of FK increased as the FK dose increased but most of the relaxation process was generally embedded within four dimensions. These findings support the existence of a circadian limit cycle oscillator in mammalian cells and suggest that a small number of variables determine the relaxation process after a perturbation. Public Library of Science 2017-07-17 /pmc/articles/PMC5513448/ /pubmed/28715496 http://dx.doi.org/10.1371/journal.pone.0181223 Text en © 2017 Koinuma 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Koinuma, Satoshi
Kori, Hiroshi
Tokuda, Isao T.
Yagita, Kazuhiro
Shigeyoshi, Yasufumi
Transition of phase response properties and singularity in the circadian limit cycle of cultured cells
title Transition of phase response properties and singularity in the circadian limit cycle of cultured cells
title_full Transition of phase response properties and singularity in the circadian limit cycle of cultured cells
title_fullStr Transition of phase response properties and singularity in the circadian limit cycle of cultured cells
title_full_unstemmed Transition of phase response properties and singularity in the circadian limit cycle of cultured cells
title_short Transition of phase response properties and singularity in the circadian limit cycle of cultured cells
title_sort transition of phase response properties and singularity in the circadian limit cycle of cultured cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5513448/
https://www.ncbi.nlm.nih.gov/pubmed/28715496
http://dx.doi.org/10.1371/journal.pone.0181223
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