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DNA sequence properties that predict susceptibility to epiallelic switching
Transgenerationally heritable epialleles are defined by the stable propagation of alternative transcriptional states through mitotic and meiotic cell cycles. Given that the propagation of DNA methylation at CpG sites, mediated in Arabidopsis by MET1, plays a central role in epigenetic inheritance, w...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331756/ https://www.ncbi.nlm.nih.gov/pubmed/28069706 http://dx.doi.org/10.15252/embj.201695602 |
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author | Catoni, Marco Griffiths, Jayne Becker, Claude Zabet, Nicolae Radu Bayon, Carlos Dapp, Mélanie Lieberman‐Lazarovich, Michal Weigel, Detlef Paszkowski, Jerzy |
author_facet | Catoni, Marco Griffiths, Jayne Becker, Claude Zabet, Nicolae Radu Bayon, Carlos Dapp, Mélanie Lieberman‐Lazarovich, Michal Weigel, Detlef Paszkowski, Jerzy |
author_sort | Catoni, Marco |
collection | PubMed |
description | Transgenerationally heritable epialleles are defined by the stable propagation of alternative transcriptional states through mitotic and meiotic cell cycles. Given that the propagation of DNA methylation at CpG sites, mediated in Arabidopsis by MET1, plays a central role in epigenetic inheritance, we examined genomewide DNA methylation in partial and complete loss‐of‐function met1 mutants. We interpreted the data in relation to transgenerational epiallelic stability, which allowed us to classify chromosomal targets of epigenetic regulation into (i) single copy and methylated exclusively at CpGs, readily forming epialleles, and (ii) transposon‐derived, methylated at all cytosines, which may or may not form epialleles. We provide evidence that DNA sequence features such as density of CpGs and genomic repetitiveness of the loci predispose their susceptibility to epiallelic switching. The importance and predictive power of these genetic features were confirmed by analyses of common epialleles in natural Arabidopsis accessions, epigenetic recombinant inbred lines (epiRILs) and also verified in rice. |
format | Online Article Text |
id | pubmed-5331756 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53317562017-03-06 DNA sequence properties that predict susceptibility to epiallelic switching Catoni, Marco Griffiths, Jayne Becker, Claude Zabet, Nicolae Radu Bayon, Carlos Dapp, Mélanie Lieberman‐Lazarovich, Michal Weigel, Detlef Paszkowski, Jerzy EMBO J Articles Transgenerationally heritable epialleles are defined by the stable propagation of alternative transcriptional states through mitotic and meiotic cell cycles. Given that the propagation of DNA methylation at CpG sites, mediated in Arabidopsis by MET1, plays a central role in epigenetic inheritance, we examined genomewide DNA methylation in partial and complete loss‐of‐function met1 mutants. We interpreted the data in relation to transgenerational epiallelic stability, which allowed us to classify chromosomal targets of epigenetic regulation into (i) single copy and methylated exclusively at CpGs, readily forming epialleles, and (ii) transposon‐derived, methylated at all cytosines, which may or may not form epialleles. We provide evidence that DNA sequence features such as density of CpGs and genomic repetitiveness of the loci predispose their susceptibility to epiallelic switching. The importance and predictive power of these genetic features were confirmed by analyses of common epialleles in natural Arabidopsis accessions, epigenetic recombinant inbred lines (epiRILs) and also verified in rice. John Wiley and Sons Inc. 2017-01-09 2017-03-01 /pmc/articles/PMC5331756/ /pubmed/28069706 http://dx.doi.org/10.15252/embj.201695602 Text en © 2017 The Authors. Published under the terms of the CC BY NC ND 4.0 license This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs 4.0 (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Articles Catoni, Marco Griffiths, Jayne Becker, Claude Zabet, Nicolae Radu Bayon, Carlos Dapp, Mélanie Lieberman‐Lazarovich, Michal Weigel, Detlef Paszkowski, Jerzy DNA sequence properties that predict susceptibility to epiallelic switching |
title |
DNA sequence properties that predict susceptibility to epiallelic switching |
title_full |
DNA sequence properties that predict susceptibility to epiallelic switching |
title_fullStr |
DNA sequence properties that predict susceptibility to epiallelic switching |
title_full_unstemmed |
DNA sequence properties that predict susceptibility to epiallelic switching |
title_short |
DNA sequence properties that predict susceptibility to epiallelic switching |
title_sort | dna sequence properties that predict susceptibility to epiallelic switching |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331756/ https://www.ncbi.nlm.nih.gov/pubmed/28069706 http://dx.doi.org/10.15252/embj.201695602 |
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