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Quantifying polymorphism and divergence from epigenetic data: a framework for inferring the action of selection

Epigenetic modifications are alterations that regulate gene expression without modifying the underlying DNA sequence. DNA methylation and histone modifications, for example, are capable of spatial and temporal regulation of expression—with several studies demonstrating that these epigenetic marks ar...

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Autores principales: Mahajan, Shivani, Crisci, Jessica, Wong, Alex, Akbarian, Schahram, Foll, Matthieu, Jensen, Jeffrey D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4446996/
https://www.ncbi.nlm.nih.gov/pubmed/26074949
http://dx.doi.org/10.3389/fgene.2015.00190
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author Mahajan, Shivani
Crisci, Jessica
Wong, Alex
Akbarian, Schahram
Foll, Matthieu
Jensen, Jeffrey D.
author_facet Mahajan, Shivani
Crisci, Jessica
Wong, Alex
Akbarian, Schahram
Foll, Matthieu
Jensen, Jeffrey D.
author_sort Mahajan, Shivani
collection PubMed
description Epigenetic modifications are alterations that regulate gene expression without modifying the underlying DNA sequence. DNA methylation and histone modifications, for example, are capable of spatial and temporal regulation of expression—with several studies demonstrating that these epigenetic marks are heritable. Thus, like DNA sequence, epigenetic marks are capable of storing information and passing it from one generation to the next. Because the epigenome is dynamic and epigenetic modifications can respond to external environmental stimuli, such changes may play an important role in adaptive evolution. While recent studies provide strong evidence for species-specific signatures of epigenetic marks, little is known about the mechanisms by which such modifications evolve. In order to address this question, we analyze the genome wide distribution of an epigenetic histone mark (H3K4me3) in prefrontal cortex neurons of humans, chimps and rhesus macaques. We develop a novel statistical framework to quantify within- and between-species variation in histone methylation patterns, using an ANOVA-based method and defining an F(ST) -like measure for epigenetics (termed epi- F(ST)), in order to develop a deeper understanding of the evolutionary pressures acting on epigenetic variation. Results demonstrate that genes with high epigenetic F(ST) values are indeed significantly overrepresented among genes that are differentially expressed between species, and we observe only a weak correlation with SNP density.
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spelling pubmed-44469962015-06-12 Quantifying polymorphism and divergence from epigenetic data: a framework for inferring the action of selection Mahajan, Shivani Crisci, Jessica Wong, Alex Akbarian, Schahram Foll, Matthieu Jensen, Jeffrey D. Front Genet Genetics Epigenetic modifications are alterations that regulate gene expression without modifying the underlying DNA sequence. DNA methylation and histone modifications, for example, are capable of spatial and temporal regulation of expression—with several studies demonstrating that these epigenetic marks are heritable. Thus, like DNA sequence, epigenetic marks are capable of storing information and passing it from one generation to the next. Because the epigenome is dynamic and epigenetic modifications can respond to external environmental stimuli, such changes may play an important role in adaptive evolution. While recent studies provide strong evidence for species-specific signatures of epigenetic marks, little is known about the mechanisms by which such modifications evolve. In order to address this question, we analyze the genome wide distribution of an epigenetic histone mark (H3K4me3) in prefrontal cortex neurons of humans, chimps and rhesus macaques. We develop a novel statistical framework to quantify within- and between-species variation in histone methylation patterns, using an ANOVA-based method and defining an F(ST) -like measure for epigenetics (termed epi- F(ST)), in order to develop a deeper understanding of the evolutionary pressures acting on epigenetic variation. Results demonstrate that genes with high epigenetic F(ST) values are indeed significantly overrepresented among genes that are differentially expressed between species, and we observe only a weak correlation with SNP density. Frontiers Media S.A. 2015-05-28 /pmc/articles/PMC4446996/ /pubmed/26074949 http://dx.doi.org/10.3389/fgene.2015.00190 Text en Copyright © 2015 Mahajan, Crisci, Wong, Akbarian, Foll and Jensen. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Mahajan, Shivani
Crisci, Jessica
Wong, Alex
Akbarian, Schahram
Foll, Matthieu
Jensen, Jeffrey D.
Quantifying polymorphism and divergence from epigenetic data: a framework for inferring the action of selection
title Quantifying polymorphism and divergence from epigenetic data: a framework for inferring the action of selection
title_full Quantifying polymorphism and divergence from epigenetic data: a framework for inferring the action of selection
title_fullStr Quantifying polymorphism and divergence from epigenetic data: a framework for inferring the action of selection
title_full_unstemmed Quantifying polymorphism and divergence from epigenetic data: a framework for inferring the action of selection
title_short Quantifying polymorphism and divergence from epigenetic data: a framework for inferring the action of selection
title_sort quantifying polymorphism and divergence from epigenetic data: a framework for inferring the action of selection
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4446996/
https://www.ncbi.nlm.nih.gov/pubmed/26074949
http://dx.doi.org/10.3389/fgene.2015.00190
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