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Functional Analysis of Casein Kinase 1 in a Minimal Circadian System
The Earth’s rotation has driven the evolution of cellular circadian clocks to facilitate anticipation of the solar cycle. Some evidence for timekeeping mechanism conserved from early unicellular life through to modern organisms was recently identified, but the components of this oscillator are curre...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3723912/ https://www.ncbi.nlm.nih.gov/pubmed/23936135 http://dx.doi.org/10.1371/journal.pone.0070021 |
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author | van Ooijen, Gerben Hindle, Matthew Martin, Sarah F. Barrios-Llerena, Martin Sanchez, Frédéric Bouget, François-Yves O’Neill, John S. Le Bihan, Thierry Millar, Andrew J. |
author_facet | van Ooijen, Gerben Hindle, Matthew Martin, Sarah F. Barrios-Llerena, Martin Sanchez, Frédéric Bouget, François-Yves O’Neill, John S. Le Bihan, Thierry Millar, Andrew J. |
author_sort | van Ooijen, Gerben |
collection | PubMed |
description | The Earth’s rotation has driven the evolution of cellular circadian clocks to facilitate anticipation of the solar cycle. Some evidence for timekeeping mechanism conserved from early unicellular life through to modern organisms was recently identified, but the components of this oscillator are currently unknown. Although very few clock components appear to be shared across higher species, Casein Kinase 1 (CK1) is known to affect timekeeping across metazoans and fungi, but has not previously been implicated in the circadian clock in the plant kingdom. We now show that modulation of CK1 function lengthens circadian rhythms in Ostreococcus tauri , a unicellular marine algal species at the base of the green lineage, separated from humans by ~1.5 billion years of evolution. CK1 contributes to timekeeping in a phase-dependent manner, indicating clock-mediated gating of CK1 activity. Label-free proteomic analyses upon overexpression as well as inhibition revealed CK1-responsive phosphorylation events on a set of target proteins, including highly conserved potentially clock-relevant cellular regulator proteins. These results have major implications for our understanding of cellular timekeeping and can inform future studies in any circadian organism. |
format | Online Article Text |
id | pubmed-3723912 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37239122013-08-09 Functional Analysis of Casein Kinase 1 in a Minimal Circadian System van Ooijen, Gerben Hindle, Matthew Martin, Sarah F. Barrios-Llerena, Martin Sanchez, Frédéric Bouget, François-Yves O’Neill, John S. Le Bihan, Thierry Millar, Andrew J. PLoS One Research Article The Earth’s rotation has driven the evolution of cellular circadian clocks to facilitate anticipation of the solar cycle. Some evidence for timekeeping mechanism conserved from early unicellular life through to modern organisms was recently identified, but the components of this oscillator are currently unknown. Although very few clock components appear to be shared across higher species, Casein Kinase 1 (CK1) is known to affect timekeeping across metazoans and fungi, but has not previously been implicated in the circadian clock in the plant kingdom. We now show that modulation of CK1 function lengthens circadian rhythms in Ostreococcus tauri , a unicellular marine algal species at the base of the green lineage, separated from humans by ~1.5 billion years of evolution. CK1 contributes to timekeeping in a phase-dependent manner, indicating clock-mediated gating of CK1 activity. Label-free proteomic analyses upon overexpression as well as inhibition revealed CK1-responsive phosphorylation events on a set of target proteins, including highly conserved potentially clock-relevant cellular regulator proteins. These results have major implications for our understanding of cellular timekeeping and can inform future studies in any circadian organism. Public Library of Science 2013-07-25 /pmc/articles/PMC3723912/ /pubmed/23936135 http://dx.doi.org/10.1371/journal.pone.0070021 Text en © 2013 van Ooijen 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 van Ooijen, Gerben Hindle, Matthew Martin, Sarah F. Barrios-Llerena, Martin Sanchez, Frédéric Bouget, François-Yves O’Neill, John S. Le Bihan, Thierry Millar, Andrew J. Functional Analysis of Casein Kinase 1 in a Minimal Circadian System |
title | Functional Analysis of Casein Kinase 1 in a Minimal Circadian System |
title_full | Functional Analysis of Casein Kinase 1 in a Minimal Circadian System |
title_fullStr | Functional Analysis of Casein Kinase 1 in a Minimal Circadian System |
title_full_unstemmed | Functional Analysis of Casein Kinase 1 in a Minimal Circadian System |
title_short | Functional Analysis of Casein Kinase 1 in a Minimal Circadian System |
title_sort | functional analysis of casein kinase 1 in a minimal circadian system |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3723912/ https://www.ncbi.nlm.nih.gov/pubmed/23936135 http://dx.doi.org/10.1371/journal.pone.0070021 |
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