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Assessing the Impact of Transgenerational Epigenetic Variation on Complex Traits

Loss or gain of DNA methylation can affect gene expression and is sometimes transmitted across generations. Such epigenetic alterations are thus a possible source of heritable phenotypic variation in the absence of DNA sequence change. However, attempts to assess the prevalence of stable epigenetic...

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Autores principales: Johannes, Frank, Porcher, Emmanuelle, Teixeira, Felipe K., Saliba-Colombani, Vera, Simon, Matthieu, Agier, Nicolas, Bulski, Agnès, Albuisson, Juliette, Heredia, Fabiana, Audigier, Pascal, Bouchez, David, Dillmann, Christine, Guerche, Philippe, Hospital, Frédéric, Colot, Vincent
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2696037/
https://www.ncbi.nlm.nih.gov/pubmed/19557164
http://dx.doi.org/10.1371/journal.pgen.1000530
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author Johannes, Frank
Porcher, Emmanuelle
Teixeira, Felipe K.
Saliba-Colombani, Vera
Simon, Matthieu
Agier, Nicolas
Bulski, Agnès
Albuisson, Juliette
Heredia, Fabiana
Audigier, Pascal
Bouchez, David
Dillmann, Christine
Guerche, Philippe
Hospital, Frédéric
Colot, Vincent
author_facet Johannes, Frank
Porcher, Emmanuelle
Teixeira, Felipe K.
Saliba-Colombani, Vera
Simon, Matthieu
Agier, Nicolas
Bulski, Agnès
Albuisson, Juliette
Heredia, Fabiana
Audigier, Pascal
Bouchez, David
Dillmann, Christine
Guerche, Philippe
Hospital, Frédéric
Colot, Vincent
author_sort Johannes, Frank
collection PubMed
description Loss or gain of DNA methylation can affect gene expression and is sometimes transmitted across generations. Such epigenetic alterations are thus a possible source of heritable phenotypic variation in the absence of DNA sequence change. However, attempts to assess the prevalence of stable epigenetic variation in natural and experimental populations and to quantify its impact on complex traits have been hampered by the confounding effects of DNA sequence polymorphisms. To overcome this problem as much as possible, two parents with little DNA sequence differences, but contrasting DNA methylation profiles, were used to derive a panel of epigenetic Recombinant Inbred Lines (epiRILs) in the reference plant Arabidopsis thaliana. The epiRILs showed variation and high heritability for flowering time and plant height (∼30%), as well as stable inheritance of multiple parental DNA methylation variants (epialleles) over at least eight generations. These findings provide a first rationale to identify epiallelic variants that contribute to heritable variation in complex traits using linkage or association studies. More generally, the demonstration that numerous epialleles across the genome can be stable over many generations in the absence of selection or extensive DNA sequence variation highlights the need to integrate epigenetic information into population genetics studies.
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spelling pubmed-26960372009-06-26 Assessing the Impact of Transgenerational Epigenetic Variation on Complex Traits Johannes, Frank Porcher, Emmanuelle Teixeira, Felipe K. Saliba-Colombani, Vera Simon, Matthieu Agier, Nicolas Bulski, Agnès Albuisson, Juliette Heredia, Fabiana Audigier, Pascal Bouchez, David Dillmann, Christine Guerche, Philippe Hospital, Frédéric Colot, Vincent PLoS Genet Research Article Loss or gain of DNA methylation can affect gene expression and is sometimes transmitted across generations. Such epigenetic alterations are thus a possible source of heritable phenotypic variation in the absence of DNA sequence change. However, attempts to assess the prevalence of stable epigenetic variation in natural and experimental populations and to quantify its impact on complex traits have been hampered by the confounding effects of DNA sequence polymorphisms. To overcome this problem as much as possible, two parents with little DNA sequence differences, but contrasting DNA methylation profiles, were used to derive a panel of epigenetic Recombinant Inbred Lines (epiRILs) in the reference plant Arabidopsis thaliana. The epiRILs showed variation and high heritability for flowering time and plant height (∼30%), as well as stable inheritance of multiple parental DNA methylation variants (epialleles) over at least eight generations. These findings provide a first rationale to identify epiallelic variants that contribute to heritable variation in complex traits using linkage or association studies. More generally, the demonstration that numerous epialleles across the genome can be stable over many generations in the absence of selection or extensive DNA sequence variation highlights the need to integrate epigenetic information into population genetics studies. Public Library of Science 2009-06-26 /pmc/articles/PMC2696037/ /pubmed/19557164 http://dx.doi.org/10.1371/journal.pgen.1000530 Text en Johannes 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
Johannes, Frank
Porcher, Emmanuelle
Teixeira, Felipe K.
Saliba-Colombani, Vera
Simon, Matthieu
Agier, Nicolas
Bulski, Agnès
Albuisson, Juliette
Heredia, Fabiana
Audigier, Pascal
Bouchez, David
Dillmann, Christine
Guerche, Philippe
Hospital, Frédéric
Colot, Vincent
Assessing the Impact of Transgenerational Epigenetic Variation on Complex Traits
title Assessing the Impact of Transgenerational Epigenetic Variation on Complex Traits
title_full Assessing the Impact of Transgenerational Epigenetic Variation on Complex Traits
title_fullStr Assessing the Impact of Transgenerational Epigenetic Variation on Complex Traits
title_full_unstemmed Assessing the Impact of Transgenerational Epigenetic Variation on Complex Traits
title_short Assessing the Impact of Transgenerational Epigenetic Variation on Complex Traits
title_sort assessing the impact of transgenerational epigenetic variation on complex traits
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2696037/
https://www.ncbi.nlm.nih.gov/pubmed/19557164
http://dx.doi.org/10.1371/journal.pgen.1000530
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