Cargando…

Evolution of H3K27me3-marked chromatin is linked to gene expression evolution and to patterns of gene duplication and diversification

Histone modifications are critical for the regulation of gene expression, cell type specification, and differentiation. However, evolutionary patterns of key modifications that regulate gene expression in differentiating organisms have not been examined. Here we mapped the genomic locations of the r...

Descripción completa

Detalles Bibliográficos
Autores principales: Arthur, Robert K., Ma, Lijia, Slattery, Matthew, Spokony, Rebecca F., Ostapenko, Alexander, Nègre, Nicolas, White, Kevin P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079967/
https://www.ncbi.nlm.nih.gov/pubmed/24985914
http://dx.doi.org/10.1101/gr.162008.113
_version_ 1782323920880271360
author Arthur, Robert K.
Ma, Lijia
Slattery, Matthew
Spokony, Rebecca F.
Ostapenko, Alexander
Nègre, Nicolas
White, Kevin P.
author_facet Arthur, Robert K.
Ma, Lijia
Slattery, Matthew
Spokony, Rebecca F.
Ostapenko, Alexander
Nègre, Nicolas
White, Kevin P.
author_sort Arthur, Robert K.
collection PubMed
description Histone modifications are critical for the regulation of gene expression, cell type specification, and differentiation. However, evolutionary patterns of key modifications that regulate gene expression in differentiating organisms have not been examined. Here we mapped the genomic locations of the repressive mark histone 3 lysine 27 trimethylation (H3K27me3) in four species of Drosophila, and compared these patterns to those in C. elegans. We found that patterns of H3K27me3 are highly conserved across species, but conservation is substantially weaker among duplicated genes. We further discovered that retropositions are associated with greater evolutionary changes in H3K27me3 and gene expression than tandem duplications, indicating that local chromatin constraints influence duplicated gene evolution. These changes are also associated with concomitant evolution of gene expression. Our findings reveal the strong conservation of genomic architecture governed by an epigenetic mark across distantly related species and the importance of gene duplication in generating novel H3K27me3 profiles.
format Online
Article
Text
id pubmed-4079967
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Cold Spring Harbor Laboratory Press
record_format MEDLINE/PubMed
spelling pubmed-40799672014-07-17 Evolution of H3K27me3-marked chromatin is linked to gene expression evolution and to patterns of gene duplication and diversification Arthur, Robert K. Ma, Lijia Slattery, Matthew Spokony, Rebecca F. Ostapenko, Alexander Nègre, Nicolas White, Kevin P. Genome Res Research Histone modifications are critical for the regulation of gene expression, cell type specification, and differentiation. However, evolutionary patterns of key modifications that regulate gene expression in differentiating organisms have not been examined. Here we mapped the genomic locations of the repressive mark histone 3 lysine 27 trimethylation (H3K27me3) in four species of Drosophila, and compared these patterns to those in C. elegans. We found that patterns of H3K27me3 are highly conserved across species, but conservation is substantially weaker among duplicated genes. We further discovered that retropositions are associated with greater evolutionary changes in H3K27me3 and gene expression than tandem duplications, indicating that local chromatin constraints influence duplicated gene evolution. These changes are also associated with concomitant evolution of gene expression. Our findings reveal the strong conservation of genomic architecture governed by an epigenetic mark across distantly related species and the importance of gene duplication in generating novel H3K27me3 profiles. Cold Spring Harbor Laboratory Press 2014-07 /pmc/articles/PMC4079967/ /pubmed/24985914 http://dx.doi.org/10.1101/gr.162008.113 Text en © 2014 Arthur et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by/4.0/ This article, published in Genome Research, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0.
spellingShingle Research
Arthur, Robert K.
Ma, Lijia
Slattery, Matthew
Spokony, Rebecca F.
Ostapenko, Alexander
Nègre, Nicolas
White, Kevin P.
Evolution of H3K27me3-marked chromatin is linked to gene expression evolution and to patterns of gene duplication and diversification
title Evolution of H3K27me3-marked chromatin is linked to gene expression evolution and to patterns of gene duplication and diversification
title_full Evolution of H3K27me3-marked chromatin is linked to gene expression evolution and to patterns of gene duplication and diversification
title_fullStr Evolution of H3K27me3-marked chromatin is linked to gene expression evolution and to patterns of gene duplication and diversification
title_full_unstemmed Evolution of H3K27me3-marked chromatin is linked to gene expression evolution and to patterns of gene duplication and diversification
title_short Evolution of H3K27me3-marked chromatin is linked to gene expression evolution and to patterns of gene duplication and diversification
title_sort evolution of h3k27me3-marked chromatin is linked to gene expression evolution and to patterns of gene duplication and diversification
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079967/
https://www.ncbi.nlm.nih.gov/pubmed/24985914
http://dx.doi.org/10.1101/gr.162008.113
work_keys_str_mv AT arthurrobertk evolutionofh3k27me3markedchromatinislinkedtogeneexpressionevolutionandtopatternsofgeneduplicationanddiversification
AT malijia evolutionofh3k27me3markedchromatinislinkedtogeneexpressionevolutionandtopatternsofgeneduplicationanddiversification
AT slatterymatthew evolutionofh3k27me3markedchromatinislinkedtogeneexpressionevolutionandtopatternsofgeneduplicationanddiversification
AT spokonyrebeccaf evolutionofh3k27me3markedchromatinislinkedtogeneexpressionevolutionandtopatternsofgeneduplicationanddiversification
AT ostapenkoalexander evolutionofh3k27me3markedchromatinislinkedtogeneexpressionevolutionandtopatternsofgeneduplicationanddiversification
AT negrenicolas evolutionofh3k27me3markedchromatinislinkedtogeneexpressionevolutionandtopatternsofgeneduplicationanddiversification
AT whitekevinp evolutionofh3k27me3markedchromatinislinkedtogeneexpressionevolutionandtopatternsofgeneduplicationanddiversification