Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Wyler, Michele, Stritt, Christoph, Walser, Jean-Claude, Baroux, Célia, Roulin, Anne C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
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
_version_ 1783606310350094336
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
work_keys_str_mv AT wylermichele impactoftransposableelementsonmethylationandgeneexpressionacrossnaturalaccessionsofbrachypodiumdistachyon
AT strittchristoph impactoftransposableelementsonmethylationandgeneexpressionacrossnaturalaccessionsofbrachypodiumdistachyon
AT walserjeanclaude impactoftransposableelementsonmethylationandgeneexpressionacrossnaturalaccessionsofbrachypodiumdistachyon
AT barouxcelia impactoftransposableelementsonmethylationandgeneexpressionacrossnaturalaccessionsofbrachypodiumdistachyon
AT roulinannec impactoftransposableelementsonmethylationandgeneexpressionacrossnaturalaccessionsofbrachypodiumdistachyon