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A stochastic oscillator model simulates the entrainment of vertebrate cellular clocks by light

The circadian clock is a cellular mechanism that synchronizes various biological processes with respect to the time of the day. While much progress has been made characterizing the molecular mechanisms underlying this clock, it is less clear how external light cues influence the dynamics of the core...

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Autores principales: Kumpošt, Vojtěch, Vallone, Daniela, Gondi, Srinivas Babu, Foulkes, Nicholas S., Mikut, Ralf, Hilbert, Lennart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8280200/
https://www.ncbi.nlm.nih.gov/pubmed/34262086
http://dx.doi.org/10.1038/s41598-021-93913-2
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author Kumpošt, Vojtěch
Vallone, Daniela
Gondi, Srinivas Babu
Foulkes, Nicholas S.
Mikut, Ralf
Hilbert, Lennart
author_facet Kumpošt, Vojtěch
Vallone, Daniela
Gondi, Srinivas Babu
Foulkes, Nicholas S.
Mikut, Ralf
Hilbert, Lennart
author_sort Kumpošt, Vojtěch
collection PubMed
description The circadian clock is a cellular mechanism that synchronizes various biological processes with respect to the time of the day. While much progress has been made characterizing the molecular mechanisms underlying this clock, it is less clear how external light cues influence the dynamics of the core clock mechanism and thereby entrain it with the light–dark cycle. Zebrafish-derived cell cultures possess clocks that are directly light-entrainable, thus providing an attractive laboratory model for circadian entrainment. Here, we have developed a stochastic oscillator model of the zebrafish circadian clock, which accounts for the core clock negative feedback loop, light input, and the proliferation of single-cell oscillator noise into population-level luminescence recordings. The model accurately predicts the entrainment dynamics observed in bioluminescent clock reporter assays upon exposure to a wide range of lighting conditions. Furthermore, we have applied the model to obtain refitted parameter sets for cell cultures exposed to a variety of pharmacological treatments and predict changes in single-cell oscillator parameters. Our work paves the way for model-based, large-scale screens for genetic or pharmacologically-induced modifications to the entrainment of circadian clock function.
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spelling pubmed-82802002021-07-15 A stochastic oscillator model simulates the entrainment of vertebrate cellular clocks by light Kumpošt, Vojtěch Vallone, Daniela Gondi, Srinivas Babu Foulkes, Nicholas S. Mikut, Ralf Hilbert, Lennart Sci Rep Article The circadian clock is a cellular mechanism that synchronizes various biological processes with respect to the time of the day. While much progress has been made characterizing the molecular mechanisms underlying this clock, it is less clear how external light cues influence the dynamics of the core clock mechanism and thereby entrain it with the light–dark cycle. Zebrafish-derived cell cultures possess clocks that are directly light-entrainable, thus providing an attractive laboratory model for circadian entrainment. Here, we have developed a stochastic oscillator model of the zebrafish circadian clock, which accounts for the core clock negative feedback loop, light input, and the proliferation of single-cell oscillator noise into population-level luminescence recordings. The model accurately predicts the entrainment dynamics observed in bioluminescent clock reporter assays upon exposure to a wide range of lighting conditions. Furthermore, we have applied the model to obtain refitted parameter sets for cell cultures exposed to a variety of pharmacological treatments and predict changes in single-cell oscillator parameters. Our work paves the way for model-based, large-scale screens for genetic or pharmacologically-induced modifications to the entrainment of circadian clock function. Nature Publishing Group UK 2021-07-14 /pmc/articles/PMC8280200/ /pubmed/34262086 http://dx.doi.org/10.1038/s41598-021-93913-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kumpošt, Vojtěch
Vallone, Daniela
Gondi, Srinivas Babu
Foulkes, Nicholas S.
Mikut, Ralf
Hilbert, Lennart
A stochastic oscillator model simulates the entrainment of vertebrate cellular clocks by light
title A stochastic oscillator model simulates the entrainment of vertebrate cellular clocks by light
title_full A stochastic oscillator model simulates the entrainment of vertebrate cellular clocks by light
title_fullStr A stochastic oscillator model simulates the entrainment of vertebrate cellular clocks by light
title_full_unstemmed A stochastic oscillator model simulates the entrainment of vertebrate cellular clocks by light
title_short A stochastic oscillator model simulates the entrainment of vertebrate cellular clocks by light
title_sort stochastic oscillator model simulates the entrainment of vertebrate cellular clocks by light
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8280200/
https://www.ncbi.nlm.nih.gov/pubmed/34262086
http://dx.doi.org/10.1038/s41598-021-93913-2
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