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Comparative analysis of genome-wide DNA methylation in Neurospora
DNA methylation is an epigenetic mark that plays an important role in genetic regulation in eukaryotes. Major progress has been made in dissecting the molecular pathways that regulate DNA methylation. Yet, little is known about DNA methylation variation over evolutionary time. Here we present an inv...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7518705/ https://www.ncbi.nlm.nih.gov/pubmed/32228351 http://dx.doi.org/10.1080/15592294.2020.1741758 |
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author | Hosseini, Sara Meunier, Cécile Nguyen, Diem Reimegård, Johan Johannesson, Hanna |
author_facet | Hosseini, Sara Meunier, Cécile Nguyen, Diem Reimegård, Johan Johannesson, Hanna |
author_sort | Hosseini, Sara |
collection | PubMed |
description | DNA methylation is an epigenetic mark that plays an important role in genetic regulation in eukaryotes. Major progress has been made in dissecting the molecular pathways that regulate DNA methylation. Yet, little is known about DNA methylation variation over evolutionary time. Here we present an investigation of the variation of DNA methylation and transposable element (TE) content in species of the filamentous ascomycetes Neurospora. We generated genome-wide DNA methylation data at single-base resolution, together with genomic TE content and gene expression data, of 10 individuals representing five closely related Neurospora species. We found that the methylation levels were low (ranging from 1.3% to 2.5%) and varied among the genomes in a species-specific way. Furthermore, we found that the TEs over 400 bp long were targeted by DNA methylation, and in all genomes, high methylation correlated with low GC, confirming a conserved link between DNA methylation and Repeat Induced Point (RIP) mutations in this group of fungi. Both TE content and DNA methylation pattern showed phylogenetic signal, and the species with the highest TE load (N. crassa) also exhibited the highest methylation level per TE. Our results suggest that DNA methylation is an evolvable trait and indicate that the genomes of Neurospora are shaped by an evolutionary arms race between TEs and host defence. |
format | Online Article Text |
id | pubmed-7518705 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-75187052020-10-01 Comparative analysis of genome-wide DNA methylation in Neurospora Hosseini, Sara Meunier, Cécile Nguyen, Diem Reimegård, Johan Johannesson, Hanna Epigenetics Research Paper DNA methylation is an epigenetic mark that plays an important role in genetic regulation in eukaryotes. Major progress has been made in dissecting the molecular pathways that regulate DNA methylation. Yet, little is known about DNA methylation variation over evolutionary time. Here we present an investigation of the variation of DNA methylation and transposable element (TE) content in species of the filamentous ascomycetes Neurospora. We generated genome-wide DNA methylation data at single-base resolution, together with genomic TE content and gene expression data, of 10 individuals representing five closely related Neurospora species. We found that the methylation levels were low (ranging from 1.3% to 2.5%) and varied among the genomes in a species-specific way. Furthermore, we found that the TEs over 400 bp long were targeted by DNA methylation, and in all genomes, high methylation correlated with low GC, confirming a conserved link between DNA methylation and Repeat Induced Point (RIP) mutations in this group of fungi. Both TE content and DNA methylation pattern showed phylogenetic signal, and the species with the highest TE load (N. crassa) also exhibited the highest methylation level per TE. Our results suggest that DNA methylation is an evolvable trait and indicate that the genomes of Neurospora are shaped by an evolutionary arms race between TEs and host defence. Taylor & Francis 2020-03-31 /pmc/articles/PMC7518705/ /pubmed/32228351 http://dx.doi.org/10.1080/15592294.2020.1741758 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
spellingShingle | Research Paper Hosseini, Sara Meunier, Cécile Nguyen, Diem Reimegård, Johan Johannesson, Hanna Comparative analysis of genome-wide DNA methylation in Neurospora |
title | Comparative analysis of genome-wide DNA methylation in Neurospora |
title_full | Comparative analysis of genome-wide DNA methylation in Neurospora |
title_fullStr | Comparative analysis of genome-wide DNA methylation in Neurospora |
title_full_unstemmed | Comparative analysis of genome-wide DNA methylation in Neurospora |
title_short | Comparative analysis of genome-wide DNA methylation in Neurospora |
title_sort | comparative analysis of genome-wide dna methylation in neurospora |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7518705/ https://www.ncbi.nlm.nih.gov/pubmed/32228351 http://dx.doi.org/10.1080/15592294.2020.1741758 |
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