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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
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.
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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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