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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2014
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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 |
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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 |
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