Comparative Analysis of Vertebrate Diurnal/Circadian Transcriptomes.

From photosynthetic bacteria to mammals, the circadian clock evolved to track diurnal rhythms and enable organisms to anticipate daily recurring changes such as temperature and light. It orchestrates a broad spectrum of physiology such as the sleep/wake and eating/fasting cycles. While we have made...

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Main Authors: Greg Boyle, Kerstin Richter, Henry D Priest, David Traver, Todd C Mockler, Jeffrey T Chang, Steve A Kay, Ghislain Breton
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5226840?pdf=render
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spelling doaj-bd05af7c1a4748e1a36955d10ba8dfb92020-11-25T00:08:00ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01121e016992310.1371/journal.pone.0169923Comparative Analysis of Vertebrate Diurnal/Circadian Transcriptomes.Greg BoyleKerstin RichterHenry D PriestDavid TraverTodd C MocklerJeffrey T ChangSteve A KayGhislain BretonFrom photosynthetic bacteria to mammals, the circadian clock evolved to track diurnal rhythms and enable organisms to anticipate daily recurring changes such as temperature and light. It orchestrates a broad spectrum of physiology such as the sleep/wake and eating/fasting cycles. While we have made tremendous advances in our understanding of the molecular details of the circadian clock mechanism and how it is synchronized with the environment, we still have rudimentary knowledge regarding its connection to help regulate diurnal physiology. One potential reason is the sheer size of the output network. Diurnal/circadian transcriptomic studies are reporting that around 10% of the expressed genome is rhythmically controlled. Zebrafish is an important model system for the study of the core circadian mechanism in vertebrate. As Zebrafish share more than 70% of its genes with human, it could also be an additional model in addition to rodent for exploring the diurnal/circadian output with potential for translational relevance. Here we performed comparative diurnal/circadian transcriptome analysis with established mouse liver and other tissue datasets. First, by combining liver tissue sampling in a 48h time series, transcription profiling using oligonucleotide arrays and bioinformatics analysis, we profiled rhythmic transcripts and identified 2609 rhythmic genes. The comparative analysis revealed interesting features of the output network regarding number of rhythmic genes, proportion of tissue specific genes and the extent of transcription factor family expression. Undoubtedly, the Zebrafish model system will help identify new vertebrate outputs and their regulators and provides leads for further characterization of the diurnal cis-regulatory network.http://europepmc.org/articles/PMC5226840?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Greg Boyle
Kerstin Richter
Henry D Priest
David Traver
Todd C Mockler
Jeffrey T Chang
Steve A Kay
Ghislain Breton
spellingShingle Greg Boyle
Kerstin Richter
Henry D Priest
David Traver
Todd C Mockler
Jeffrey T Chang
Steve A Kay
Ghislain Breton
Comparative Analysis of Vertebrate Diurnal/Circadian Transcriptomes.
PLoS ONE
author_facet Greg Boyle
Kerstin Richter
Henry D Priest
David Traver
Todd C Mockler
Jeffrey T Chang
Steve A Kay
Ghislain Breton
author_sort Greg Boyle
title Comparative Analysis of Vertebrate Diurnal/Circadian Transcriptomes.
title_short Comparative Analysis of Vertebrate Diurnal/Circadian Transcriptomes.
title_full Comparative Analysis of Vertebrate Diurnal/Circadian Transcriptomes.
title_fullStr Comparative Analysis of Vertebrate Diurnal/Circadian Transcriptomes.
title_full_unstemmed Comparative Analysis of Vertebrate Diurnal/Circadian Transcriptomes.
title_sort comparative analysis of vertebrate diurnal/circadian transcriptomes.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
description From photosynthetic bacteria to mammals, the circadian clock evolved to track diurnal rhythms and enable organisms to anticipate daily recurring changes such as temperature and light. It orchestrates a broad spectrum of physiology such as the sleep/wake and eating/fasting cycles. While we have made tremendous advances in our understanding of the molecular details of the circadian clock mechanism and how it is synchronized with the environment, we still have rudimentary knowledge regarding its connection to help regulate diurnal physiology. One potential reason is the sheer size of the output network. Diurnal/circadian transcriptomic studies are reporting that around 10% of the expressed genome is rhythmically controlled. Zebrafish is an important model system for the study of the core circadian mechanism in vertebrate. As Zebrafish share more than 70% of its genes with human, it could also be an additional model in addition to rodent for exploring the diurnal/circadian output with potential for translational relevance. Here we performed comparative diurnal/circadian transcriptome analysis with established mouse liver and other tissue datasets. First, by combining liver tissue sampling in a 48h time series, transcription profiling using oligonucleotide arrays and bioinformatics analysis, we profiled rhythmic transcripts and identified 2609 rhythmic genes. The comparative analysis revealed interesting features of the output network regarding number of rhythmic genes, proportion of tissue specific genes and the extent of transcription factor family expression. Undoubtedly, the Zebrafish model system will help identify new vertebrate outputs and their regulators and provides leads for further characterization of the diurnal cis-regulatory network.
url http://europepmc.org/articles/PMC5226840?pdf=render
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