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Stress affects the epigenetic marks added by natural transposable element insertions in Drosophila melanogaster

Transposable elements are emerging as an important source of cis-acting regulatory sequences and epigenetic marks that could influence gene expression. However, few studies have dissected the role of specific transposable element insertions on epigenetic gene regulation. Bari-Jheh is a natural trans...

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Autores principales: Guio, Lain, Vieira, Cristina, González, Josefa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6093896/
https://www.ncbi.nlm.nih.gov/pubmed/30111890
http://dx.doi.org/10.1038/s41598-018-30491-w
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author Guio, Lain
Vieira, Cristina
González, Josefa
author_facet Guio, Lain
Vieira, Cristina
González, Josefa
author_sort Guio, Lain
collection PubMed
description Transposable elements are emerging as an important source of cis-acting regulatory sequences and epigenetic marks that could influence gene expression. However, few studies have dissected the role of specific transposable element insertions on epigenetic gene regulation. Bari-Jheh is a natural transposon that mediates resistance to oxidative stress by adding cis-regulatory sequences that affect expression of nearby genes. In this work, we integrated publicly available ChIP-seq and piRNA data with chromatin immunoprecipitation experiments to get a more comprehensive picture of Bari-Jheh molecular effects. We showed that Bari-Jheh was enriched for H3K9me3 in nonstress conditions, and for H3K9me3, H3K4me3 and H3K27me3 in oxidative stress conditions, which is consistent with expression changes in adjacent genes. We further showed that under oxidative stress conditions, H3K4me3 and H3K9me3 spread to the promoter region of Jheh1 gene. Finally, another insertion of the Bari1 family was associated with increased H3K27me3 in oxidative stress conditions suggesting that Bari1 histone marks are copy-specific. We concluded that besides adding cis-regulatory sequences, Bari-Jheh influences gene expression by affecting the local chromatin state.
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spelling pubmed-60938962018-08-20 Stress affects the epigenetic marks added by natural transposable element insertions in Drosophila melanogaster Guio, Lain Vieira, Cristina González, Josefa Sci Rep Article Transposable elements are emerging as an important source of cis-acting regulatory sequences and epigenetic marks that could influence gene expression. However, few studies have dissected the role of specific transposable element insertions on epigenetic gene regulation. Bari-Jheh is a natural transposon that mediates resistance to oxidative stress by adding cis-regulatory sequences that affect expression of nearby genes. In this work, we integrated publicly available ChIP-seq and piRNA data with chromatin immunoprecipitation experiments to get a more comprehensive picture of Bari-Jheh molecular effects. We showed that Bari-Jheh was enriched for H3K9me3 in nonstress conditions, and for H3K9me3, H3K4me3 and H3K27me3 in oxidative stress conditions, which is consistent with expression changes in adjacent genes. We further showed that under oxidative stress conditions, H3K4me3 and H3K9me3 spread to the promoter region of Jheh1 gene. Finally, another insertion of the Bari1 family was associated with increased H3K27me3 in oxidative stress conditions suggesting that Bari1 histone marks are copy-specific. We concluded that besides adding cis-regulatory sequences, Bari-Jheh influences gene expression by affecting the local chromatin state. Nature Publishing Group UK 2018-08-15 /pmc/articles/PMC6093896/ /pubmed/30111890 http://dx.doi.org/10.1038/s41598-018-30491-w Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Guio, Lain
Vieira, Cristina
González, Josefa
Stress affects the epigenetic marks added by natural transposable element insertions in Drosophila melanogaster
title Stress affects the epigenetic marks added by natural transposable element insertions in Drosophila melanogaster
title_full Stress affects the epigenetic marks added by natural transposable element insertions in Drosophila melanogaster
title_fullStr Stress affects the epigenetic marks added by natural transposable element insertions in Drosophila melanogaster
title_full_unstemmed Stress affects the epigenetic marks added by natural transposable element insertions in Drosophila melanogaster
title_short Stress affects the epigenetic marks added by natural transposable element insertions in Drosophila melanogaster
title_sort stress affects the epigenetic marks added by natural transposable element insertions in drosophila melanogaster
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6093896/
https://www.ncbi.nlm.nih.gov/pubmed/30111890
http://dx.doi.org/10.1038/s41598-018-30491-w
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