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Evolution of the repression mechanisms in circadian clocks
BACKGROUND: Circadian (daily) timekeeping is essential to the survival of many organisms. An integral part of all circadian timekeeping systems is negative feedback between an activator and repressor. However, the role of this feedback varies widely between lower and higher organisms. RESULTS: Here,...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8751359/ https://www.ncbi.nlm.nih.gov/pubmed/35012616 http://dx.doi.org/10.1186/s13059-021-02571-0 |
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author | Tyler, Jonathan Lu, Yining Dunlap, Jay Forger, Daniel B. |
author_facet | Tyler, Jonathan Lu, Yining Dunlap, Jay Forger, Daniel B. |
author_sort | Tyler, Jonathan |
collection | PubMed |
description | BACKGROUND: Circadian (daily) timekeeping is essential to the survival of many organisms. An integral part of all circadian timekeeping systems is negative feedback between an activator and repressor. However, the role of this feedback varies widely between lower and higher organisms. RESULTS: Here, we study repression mechanisms in the cyanobacterial and eukaryotic clocks through mathematical modeling and systems analysis. We find a common mathematical model that describes the mechanism by which organisms generate rhythms; however, transcription’s role in this has diverged. In cyanobacteria, protein sequestration and phosphorylation generate and regulate rhythms while transcription regulation keeps proteins in proper stoichiometric balance. Based on recent experimental work, we propose a repressor phospholock mechanism that models the negative feedback through transcription in clocks of higher organisms. Interestingly, this model, when coupled with activator phosphorylation, allows for oscillations over a wide range of protein stoichiometries, thereby reconciling the negative feedback mechanism in Neurospora with that in mammals and cyanobacteria. CONCLUSIONS: Taken together, these results paint a picture of how circadian timekeeping may have evolved. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at (10.1186/s13059-021-02571-0). |
format | Online Article Text |
id | pubmed-8751359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-87513592022-01-12 Evolution of the repression mechanisms in circadian clocks Tyler, Jonathan Lu, Yining Dunlap, Jay Forger, Daniel B. Genome Biol Research BACKGROUND: Circadian (daily) timekeeping is essential to the survival of many organisms. An integral part of all circadian timekeeping systems is negative feedback between an activator and repressor. However, the role of this feedback varies widely between lower and higher organisms. RESULTS: Here, we study repression mechanisms in the cyanobacterial and eukaryotic clocks through mathematical modeling and systems analysis. We find a common mathematical model that describes the mechanism by which organisms generate rhythms; however, transcription’s role in this has diverged. In cyanobacteria, protein sequestration and phosphorylation generate and regulate rhythms while transcription regulation keeps proteins in proper stoichiometric balance. Based on recent experimental work, we propose a repressor phospholock mechanism that models the negative feedback through transcription in clocks of higher organisms. Interestingly, this model, when coupled with activator phosphorylation, allows for oscillations over a wide range of protein stoichiometries, thereby reconciling the negative feedback mechanism in Neurospora with that in mammals and cyanobacteria. CONCLUSIONS: Taken together, these results paint a picture of how circadian timekeeping may have evolved. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at (10.1186/s13059-021-02571-0). BioMed Central 2022-01-10 /pmc/articles/PMC8751359/ /pubmed/35012616 http://dx.doi.org/10.1186/s13059-021-02571-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Tyler, Jonathan Lu, Yining Dunlap, Jay Forger, Daniel B. Evolution of the repression mechanisms in circadian clocks |
title | Evolution of the repression mechanisms in circadian clocks |
title_full | Evolution of the repression mechanisms in circadian clocks |
title_fullStr | Evolution of the repression mechanisms in circadian clocks |
title_full_unstemmed | Evolution of the repression mechanisms in circadian clocks |
title_short | Evolution of the repression mechanisms in circadian clocks |
title_sort | evolution of the repression mechanisms in circadian clocks |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8751359/ https://www.ncbi.nlm.nih.gov/pubmed/35012616 http://dx.doi.org/10.1186/s13059-021-02571-0 |
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