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Impact of Transposable Elements on Methylation and Gene Expression across Natural Accessions of Brachypodium distachyon
Transposable elements (TEs) constitute a large fraction of plant genomes and are mostly present in a transcriptionally silent state through repressive epigenetic modifications, such as DNA methylation. TE silencing is believed to influence the regulation of adjacent genes, possibly as DNA methylatio...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643609/ https://www.ncbi.nlm.nih.gov/pubmed/32853352 http://dx.doi.org/10.1093/gbe/evaa180 |
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author | Wyler, Michele Stritt, Christoph Walser, Jean-Claude Baroux, Célia Roulin, Anne C |
author_facet | Wyler, Michele Stritt, Christoph Walser, Jean-Claude Baroux, Célia Roulin, Anne C |
author_sort | Wyler, Michele |
collection | PubMed |
description | Transposable elements (TEs) constitute a large fraction of plant genomes and are mostly present in a transcriptionally silent state through repressive epigenetic modifications, such as DNA methylation. TE silencing is believed to influence the regulation of adjacent genes, possibly as DNA methylation spreads away from the TE. Whether this is a general principle or a context-dependent phenomenon is still under debate, pressing for studying the relationship between TEs, DNA methylation, and nearby gene expression in additional plant species. Here, we used the grass Brachypodium distachyon as a model and produced DNA methylation and transcriptome profiles for 11 natural accessions. In contrast to what is observed in Arabidopsis thaliana, we found that TEs have a limited impact on methylation spreading and that only few TE families are associated with a low expression of their adjacent genes. Interestingly, we found that a subset of TE insertion polymorphisms is associated with differential gene expression across accessions. Thus, although not having a global impact on gene expression, distinct TE insertions may contribute to specific gene expression patterns in B. distachyon. |
format | Online Article Text |
id | pubmed-7643609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-76436092020-11-12 Impact of Transposable Elements on Methylation and Gene Expression across Natural Accessions of Brachypodium distachyon Wyler, Michele Stritt, Christoph Walser, Jean-Claude Baroux, Célia Roulin, Anne C Genome Biol Evol Letter Transposable elements (TEs) constitute a large fraction of plant genomes and are mostly present in a transcriptionally silent state through repressive epigenetic modifications, such as DNA methylation. TE silencing is believed to influence the regulation of adjacent genes, possibly as DNA methylation spreads away from the TE. Whether this is a general principle or a context-dependent phenomenon is still under debate, pressing for studying the relationship between TEs, DNA methylation, and nearby gene expression in additional plant species. Here, we used the grass Brachypodium distachyon as a model and produced DNA methylation and transcriptome profiles for 11 natural accessions. In contrast to what is observed in Arabidopsis thaliana, we found that TEs have a limited impact on methylation spreading and that only few TE families are associated with a low expression of their adjacent genes. Interestingly, we found that a subset of TE insertion polymorphisms is associated with differential gene expression across accessions. Thus, although not having a global impact on gene expression, distinct TE insertions may contribute to specific gene expression patterns in B. distachyon. Oxford University Press 2020-08-27 /pmc/articles/PMC7643609/ /pubmed/32853352 http://dx.doi.org/10.1093/gbe/evaa180 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Letter Wyler, Michele Stritt, Christoph Walser, Jean-Claude Baroux, Célia Roulin, Anne C Impact of Transposable Elements on Methylation and Gene Expression across Natural Accessions of Brachypodium distachyon |
title | Impact of Transposable Elements on Methylation and Gene Expression across Natural Accessions of Brachypodium distachyon |
title_full | Impact of Transposable Elements on Methylation and Gene Expression across Natural Accessions of Brachypodium distachyon |
title_fullStr | Impact of Transposable Elements on Methylation and Gene Expression across Natural Accessions of Brachypodium distachyon |
title_full_unstemmed | Impact of Transposable Elements on Methylation and Gene Expression across Natural Accessions of Brachypodium distachyon |
title_short | Impact of Transposable Elements on Methylation and Gene Expression across Natural Accessions of Brachypodium distachyon |
title_sort | impact of transposable elements on methylation and gene expression across natural accessions of brachypodium distachyon |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643609/ https://www.ncbi.nlm.nih.gov/pubmed/32853352 http://dx.doi.org/10.1093/gbe/evaa180 |
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