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Signatures of DNA Methylation across Insects Suggest Reduced DNA Methylation Levels in Holometabola

It has been experimentally shown that DNA methylation is involved in the regulation of gene expression and the silencing of transposable element activity in eukaryotes. The variable levels of DNA methylation among different insect species indicate an evolutionarily flexible role of DNA methylation i...

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Autores principales: Provataris, Panagiotis, Meusemann, Karen, Niehuis, Oliver, Grath, Sonja, Misof, Bernhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915941/
https://www.ncbi.nlm.nih.gov/pubmed/29697817
http://dx.doi.org/10.1093/gbe/evy066
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author Provataris, Panagiotis
Meusemann, Karen
Niehuis, Oliver
Grath, Sonja
Misof, Bernhard
author_facet Provataris, Panagiotis
Meusemann, Karen
Niehuis, Oliver
Grath, Sonja
Misof, Bernhard
author_sort Provataris, Panagiotis
collection PubMed
description It has been experimentally shown that DNA methylation is involved in the regulation of gene expression and the silencing of transposable element activity in eukaryotes. The variable levels of DNA methylation among different insect species indicate an evolutionarily flexible role of DNA methylation in insects, which due to a lack of comparative data is not yet well-substantiated. Here, we use computational methods to trace signatures of DNA methylation across insects by analyzing transcriptomic and genomic sequence data from all currently recognized insect orders. We conclude that: 1) a functional methylation system relying exclusively on DNA methyltransferase 1 is widespread across insects. 2) DNA methylation has potentially been lost or extremely reduced in species belonging to springtails (Collembola), flies and relatives (Diptera), and twisted-winged parasites (Strepsiptera). 3) Holometabolous insects display signs of reduced DNA methylation levels in protein-coding sequences compared with hemimetabolous insects. 4) Evolutionarily conserved insect genes associated with housekeeping functions tend to display signs of heavier DNA methylation in comparison to the genomic/transcriptomic background. With this comparative study, we provide the much needed basis for experimental and detailed comparative analyses required to gain a deeper understanding on the evolution and function of DNA methylation in insects.
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spelling pubmed-59159412018-04-30 Signatures of DNA Methylation across Insects Suggest Reduced DNA Methylation Levels in Holometabola Provataris, Panagiotis Meusemann, Karen Niehuis, Oliver Grath, Sonja Misof, Bernhard Genome Biol Evol Research Article It has been experimentally shown that DNA methylation is involved in the regulation of gene expression and the silencing of transposable element activity in eukaryotes. The variable levels of DNA methylation among different insect species indicate an evolutionarily flexible role of DNA methylation in insects, which due to a lack of comparative data is not yet well-substantiated. Here, we use computational methods to trace signatures of DNA methylation across insects by analyzing transcriptomic and genomic sequence data from all currently recognized insect orders. We conclude that: 1) a functional methylation system relying exclusively on DNA methyltransferase 1 is widespread across insects. 2) DNA methylation has potentially been lost or extremely reduced in species belonging to springtails (Collembola), flies and relatives (Diptera), and twisted-winged parasites (Strepsiptera). 3) Holometabolous insects display signs of reduced DNA methylation levels in protein-coding sequences compared with hemimetabolous insects. 4) Evolutionarily conserved insect genes associated with housekeeping functions tend to display signs of heavier DNA methylation in comparison to the genomic/transcriptomic background. With this comparative study, we provide the much needed basis for experimental and detailed comparative analyses required to gain a deeper understanding on the evolution and function of DNA methylation in insects. Oxford University Press 2018-03-19 /pmc/articles/PMC5915941/ /pubmed/29697817 http://dx.doi.org/10.1093/gbe/evy066 Text en © The Author(s) 2018. 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 Research Article
Provataris, Panagiotis
Meusemann, Karen
Niehuis, Oliver
Grath, Sonja
Misof, Bernhard
Signatures of DNA Methylation across Insects Suggest Reduced DNA Methylation Levels in Holometabola
title Signatures of DNA Methylation across Insects Suggest Reduced DNA Methylation Levels in Holometabola
title_full Signatures of DNA Methylation across Insects Suggest Reduced DNA Methylation Levels in Holometabola
title_fullStr Signatures of DNA Methylation across Insects Suggest Reduced DNA Methylation Levels in Holometabola
title_full_unstemmed Signatures of DNA Methylation across Insects Suggest Reduced DNA Methylation Levels in Holometabola
title_short Signatures of DNA Methylation across Insects Suggest Reduced DNA Methylation Levels in Holometabola
title_sort signatures of dna methylation across insects suggest reduced dna methylation levels in holometabola
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915941/
https://www.ncbi.nlm.nih.gov/pubmed/29697817
http://dx.doi.org/10.1093/gbe/evy066
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