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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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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. |
format | Online Article Text |
id | pubmed-5915941 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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