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The Proteomic Landscape of the Suprachiasmatic Nucleus Clock Reveals Large-Scale Coordination of Key Biological Processes

The suprachiasmatic nucleus (SCN) acts as the central clock to coordinate circadian oscillations in mammalian behavior, physiology and gene expression. Despite our knowledge of the circadian transcriptome of the SCN, how it impacts genome-wide protein expression is not well understood. Here, we inte...

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Autores principales: Chiang, Cheng-Kang, Mehta, Neel, Patel, Abhilasha, Zhang, Peng, Ning, Zhibin, Mayne, Janice, Sun, Warren Y. L., Cheng, Hai-Ying M., Figeys, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4199512/
https://www.ncbi.nlm.nih.gov/pubmed/25330117
http://dx.doi.org/10.1371/journal.pgen.1004695
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author Chiang, Cheng-Kang
Mehta, Neel
Patel, Abhilasha
Zhang, Peng
Ning, Zhibin
Mayne, Janice
Sun, Warren Y. L.
Cheng, Hai-Ying M.
Figeys, Daniel
author_facet Chiang, Cheng-Kang
Mehta, Neel
Patel, Abhilasha
Zhang, Peng
Ning, Zhibin
Mayne, Janice
Sun, Warren Y. L.
Cheng, Hai-Ying M.
Figeys, Daniel
author_sort Chiang, Cheng-Kang
collection PubMed
description The suprachiasmatic nucleus (SCN) acts as the central clock to coordinate circadian oscillations in mammalian behavior, physiology and gene expression. Despite our knowledge of the circadian transcriptome of the SCN, how it impacts genome-wide protein expression is not well understood. Here, we interrogated the murine SCN proteome across the circadian cycle using SILAC-based quantitative mass spectrometry. Of the 2112 proteins that were accurately quantified, 20% (421 proteins) displayed a time-of-day-dependent expression profile. Within this time-of-day proteome, 11% (48 proteins) were further defined as circadian based on a sinusoidal expression pattern with a ∼24 h period. Nine circadianly expressed proteins exhibited 24 h rhythms at the transcript level, with an average time lag that exceeded 8 h. A substantial proportion of the time-of-day proteome exhibited abrupt fluctuations at the anticipated light-to-dark and dark-to-light transitions, and was enriched for proteins involved in several key biological pathways, most notably, mitochondrial oxidative phosphorylation. Additionally, predicted targets of miR-133ab were enriched in specific hierarchical clusters and were inversely correlated with miR133ab expression in the SCN. These insights into the proteomic landscape of the SCN will facilitate a more integrative understanding of cellular control within the SCN clock.
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spelling pubmed-41995122014-10-21 The Proteomic Landscape of the Suprachiasmatic Nucleus Clock Reveals Large-Scale Coordination of Key Biological Processes Chiang, Cheng-Kang Mehta, Neel Patel, Abhilasha Zhang, Peng Ning, Zhibin Mayne, Janice Sun, Warren Y. L. Cheng, Hai-Ying M. Figeys, Daniel PLoS Genet Research Article The suprachiasmatic nucleus (SCN) acts as the central clock to coordinate circadian oscillations in mammalian behavior, physiology and gene expression. Despite our knowledge of the circadian transcriptome of the SCN, how it impacts genome-wide protein expression is not well understood. Here, we interrogated the murine SCN proteome across the circadian cycle using SILAC-based quantitative mass spectrometry. Of the 2112 proteins that were accurately quantified, 20% (421 proteins) displayed a time-of-day-dependent expression profile. Within this time-of-day proteome, 11% (48 proteins) were further defined as circadian based on a sinusoidal expression pattern with a ∼24 h period. Nine circadianly expressed proteins exhibited 24 h rhythms at the transcript level, with an average time lag that exceeded 8 h. A substantial proportion of the time-of-day proteome exhibited abrupt fluctuations at the anticipated light-to-dark and dark-to-light transitions, and was enriched for proteins involved in several key biological pathways, most notably, mitochondrial oxidative phosphorylation. Additionally, predicted targets of miR-133ab were enriched in specific hierarchical clusters and were inversely correlated with miR133ab expression in the SCN. These insights into the proteomic landscape of the SCN will facilitate a more integrative understanding of cellular control within the SCN clock. Public Library of Science 2014-10-16 /pmc/articles/PMC4199512/ /pubmed/25330117 http://dx.doi.org/10.1371/journal.pgen.1004695 Text en © 2014 Chiang 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
Chiang, Cheng-Kang
Mehta, Neel
Patel, Abhilasha
Zhang, Peng
Ning, Zhibin
Mayne, Janice
Sun, Warren Y. L.
Cheng, Hai-Ying M.
Figeys, Daniel
The Proteomic Landscape of the Suprachiasmatic Nucleus Clock Reveals Large-Scale Coordination of Key Biological Processes
title The Proteomic Landscape of the Suprachiasmatic Nucleus Clock Reveals Large-Scale Coordination of Key Biological Processes
title_full The Proteomic Landscape of the Suprachiasmatic Nucleus Clock Reveals Large-Scale Coordination of Key Biological Processes
title_fullStr The Proteomic Landscape of the Suprachiasmatic Nucleus Clock Reveals Large-Scale Coordination of Key Biological Processes
title_full_unstemmed The Proteomic Landscape of the Suprachiasmatic Nucleus Clock Reveals Large-Scale Coordination of Key Biological Processes
title_short The Proteomic Landscape of the Suprachiasmatic Nucleus Clock Reveals Large-Scale Coordination of Key Biological Processes
title_sort proteomic landscape of the suprachiasmatic nucleus clock reveals large-scale coordination of key biological processes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4199512/
https://www.ncbi.nlm.nih.gov/pubmed/25330117
http://dx.doi.org/10.1371/journal.pgen.1004695
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