Cargando…

Evolution of DNA Methylation Across Ecdysozoa

DNA methylation is a crucial, abundant mechanism of gene regulation in vertebrates. It is less prevalent in many other metazoan organisms and completely absent in some key model species, such as Drosophila melanogaster and Caenorhabditis elegans. We report here a comprehensive study of the presence...

Descripción completa

Detalles Bibliográficos
Autores principales: Engelhardt, Jan, Scheer, Oliver, Stadler, Peter F., Prohaska, Sonja J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8821070/
https://www.ncbi.nlm.nih.gov/pubmed/35089376
http://dx.doi.org/10.1007/s00239-021-10042-0
_version_ 1784646343258537984
author Engelhardt, Jan
Scheer, Oliver
Stadler, Peter F.
Prohaska, Sonja J.
author_facet Engelhardt, Jan
Scheer, Oliver
Stadler, Peter F.
Prohaska, Sonja J.
author_sort Engelhardt, Jan
collection PubMed
description DNA methylation is a crucial, abundant mechanism of gene regulation in vertebrates. It is less prevalent in many other metazoan organisms and completely absent in some key model species, such as Drosophila melanogaster and Caenorhabditis elegans. We report here a comprehensive study of the presence and absence of DNA methyltransferases (DNMTs) in 138 Ecdysozoa, covering Arthropoda, Nematoda, Priapulida, Onychophora, and Tardigrada. Three of these phyla have not been investigated for the presence of DNA methylation before. We observe that the loss of individual DNMTs independently occurred multiple times across ecdysozoan phyla. We computationally predict the presence of DNA methylation based on CpG rates in coding sequences using an implementation of Gaussian Mixture Modeling, MethMod. Integrating both analysis we predict two previously unknown losses of DNA methylation in Ecdysozoa, one within Chelicerata (Mesostigmata) and one in Tardigrada. In the early-branching Ecdysozoa Priapulus caudatus, we predict the presence of a full set of DNMTs and the presence of DNA methylation. We are therefore showing a very diverse and independent evolution of DNA methylation in different ecdysozoan phyla spanning a phylogenetic range of more than 700 million years. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00239-021-10042-0.
format Online
Article
Text
id pubmed-8821070
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-88210702022-02-23 Evolution of DNA Methylation Across Ecdysozoa Engelhardt, Jan Scheer, Oliver Stadler, Peter F. Prohaska, Sonja J. J Mol Evol Original Article DNA methylation is a crucial, abundant mechanism of gene regulation in vertebrates. It is less prevalent in many other metazoan organisms and completely absent in some key model species, such as Drosophila melanogaster and Caenorhabditis elegans. We report here a comprehensive study of the presence and absence of DNA methyltransferases (DNMTs) in 138 Ecdysozoa, covering Arthropoda, Nematoda, Priapulida, Onychophora, and Tardigrada. Three of these phyla have not been investigated for the presence of DNA methylation before. We observe that the loss of individual DNMTs independently occurred multiple times across ecdysozoan phyla. We computationally predict the presence of DNA methylation based on CpG rates in coding sequences using an implementation of Gaussian Mixture Modeling, MethMod. Integrating both analysis we predict two previously unknown losses of DNA methylation in Ecdysozoa, one within Chelicerata (Mesostigmata) and one in Tardigrada. In the early-branching Ecdysozoa Priapulus caudatus, we predict the presence of a full set of DNMTs and the presence of DNA methylation. We are therefore showing a very diverse and independent evolution of DNA methylation in different ecdysozoan phyla spanning a phylogenetic range of more than 700 million years. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00239-021-10042-0. Springer US 2022-01-28 2022 /pmc/articles/PMC8821070/ /pubmed/35089376 http://dx.doi.org/10.1007/s00239-021-10042-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Engelhardt, Jan
Scheer, Oliver
Stadler, Peter F.
Prohaska, Sonja J.
Evolution of DNA Methylation Across Ecdysozoa
title Evolution of DNA Methylation Across Ecdysozoa
title_full Evolution of DNA Methylation Across Ecdysozoa
title_fullStr Evolution of DNA Methylation Across Ecdysozoa
title_full_unstemmed Evolution of DNA Methylation Across Ecdysozoa
title_short Evolution of DNA Methylation Across Ecdysozoa
title_sort evolution of dna methylation across ecdysozoa
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8821070/
https://www.ncbi.nlm.nih.gov/pubmed/35089376
http://dx.doi.org/10.1007/s00239-021-10042-0
work_keys_str_mv AT engelhardtjan evolutionofdnamethylationacrossecdysozoa
AT scheeroliver evolutionofdnamethylationacrossecdysozoa
AT stadlerpeterf evolutionofdnamethylationacrossecdysozoa
AT prohaskasonjaj evolutionofdnamethylationacrossecdysozoa