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Evolution of DNMT2 in drosophilids: Evidence for positive and purifying selection and insights into new protein (pathways) interactions

The DNA methyltransferase 2 (DNMT2) protein is the most conserved member of the DNA methyltransferase family. Nevertheless, its substrate specificity is still controversial and elusive. The genomic role and determinants of DNA methylation are poorly understood in invertebrates, and several mechanism...

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Autores principales: Vieira, Gilberto Cavalheiro, D’Ávila, Marícia Fantinel, Zanini, Rebeca, Deprá, Maríndia, da Silva Valente, Vera Lúcia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Genética 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913717/
https://www.ncbi.nlm.nih.gov/pubmed/29668012
http://dx.doi.org/10.1590/1678-4685-GMB-2017-0056
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author Vieira, Gilberto Cavalheiro
D’Ávila, Marícia Fantinel
Zanini, Rebeca
Deprá, Maríndia
da Silva Valente, Vera Lúcia
author_facet Vieira, Gilberto Cavalheiro
D’Ávila, Marícia Fantinel
Zanini, Rebeca
Deprá, Maríndia
da Silva Valente, Vera Lúcia
author_sort Vieira, Gilberto Cavalheiro
collection PubMed
description The DNA methyltransferase 2 (DNMT2) protein is the most conserved member of the DNA methyltransferase family. Nevertheless, its substrate specificity is still controversial and elusive. The genomic role and determinants of DNA methylation are poorly understood in invertebrates, and several mechanisms and associations are suggested. In Drosophila, the only known DNMT gene is Dnmt2. Here we present our findings from a wide search for Dnmt2 homologs in 68 species of Drosophilidae. We investigated its molecular evolution, and in our phylogenetic analyses the main clades of Drosophilidae species were recovered. We tested whether the Dnmt2 has evolved neutrally or under positive selection along the subgenera Drosophila and Sophophora and investigated positive selection in relation to several physicochemical properties. Despite of a major selective constraint on Dnmt2, we detected six sites under positive selection. Regarding the DNMT2 protein, 12 sites under positive-destabilizing selection were found, which suggests a selection that favors structural and functional shifts in the protein. The search for new potential protein partners with DNMT2 revealed 15 proteins with high evolutionary rate covariation (ERC), indicating a plurality of DNMT2 functions in different pathways. These events might represent signs of molecular adaptation, with molecular peculiarities arising from the diversity of evolutionary histories experienced by drosophilids.
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spelling pubmed-59137172018-05-04 Evolution of DNMT2 in drosophilids: Evidence for positive and purifying selection and insights into new protein (pathways) interactions Vieira, Gilberto Cavalheiro D’Ávila, Marícia Fantinel Zanini, Rebeca Deprá, Maríndia da Silva Valente, Vera Lúcia Genet Mol Biol Research Articles The DNA methyltransferase 2 (DNMT2) protein is the most conserved member of the DNA methyltransferase family. Nevertheless, its substrate specificity is still controversial and elusive. The genomic role and determinants of DNA methylation are poorly understood in invertebrates, and several mechanisms and associations are suggested. In Drosophila, the only known DNMT gene is Dnmt2. Here we present our findings from a wide search for Dnmt2 homologs in 68 species of Drosophilidae. We investigated its molecular evolution, and in our phylogenetic analyses the main clades of Drosophilidae species were recovered. We tested whether the Dnmt2 has evolved neutrally or under positive selection along the subgenera Drosophila and Sophophora and investigated positive selection in relation to several physicochemical properties. Despite of a major selective constraint on Dnmt2, we detected six sites under positive selection. Regarding the DNMT2 protein, 12 sites under positive-destabilizing selection were found, which suggests a selection that favors structural and functional shifts in the protein. The search for new potential protein partners with DNMT2 revealed 15 proteins with high evolutionary rate covariation (ERC), indicating a plurality of DNMT2 functions in different pathways. These events might represent signs of molecular adaptation, with molecular peculiarities arising from the diversity of evolutionary histories experienced by drosophilids. Sociedade Brasileira de Genética 2018-03-26 2018 /pmc/articles/PMC5913717/ /pubmed/29668012 http://dx.doi.org/10.1590/1678-4685-GMB-2017-0056 Text en Copyright © 2018, Sociedade Brasileira de Genética. https://creativecommons.org/licenses/by/4.0/ License information: This is an open-access article distributed under the terms of the Creative Commons Attribution License (type CC-BY), which permits unrestricted use, distribution and reproduction in any medium, provided the original article is properly cited.
spellingShingle Research Articles
Vieira, Gilberto Cavalheiro
D’Ávila, Marícia Fantinel
Zanini, Rebeca
Deprá, Maríndia
da Silva Valente, Vera Lúcia
Evolution of DNMT2 in drosophilids: Evidence for positive and purifying selection and insights into new protein (pathways) interactions
title Evolution of DNMT2 in drosophilids: Evidence for positive and purifying selection and insights into new protein (pathways) interactions
title_full Evolution of DNMT2 in drosophilids: Evidence for positive and purifying selection and insights into new protein (pathways) interactions
title_fullStr Evolution of DNMT2 in drosophilids: Evidence for positive and purifying selection and insights into new protein (pathways) interactions
title_full_unstemmed Evolution of DNMT2 in drosophilids: Evidence for positive and purifying selection and insights into new protein (pathways) interactions
title_short Evolution of DNMT2 in drosophilids: Evidence for positive and purifying selection and insights into new protein (pathways) interactions
title_sort evolution of dnmt2 in drosophilids: evidence for positive and purifying selection and insights into new protein (pathways) interactions
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913717/
https://www.ncbi.nlm.nih.gov/pubmed/29668012
http://dx.doi.org/10.1590/1678-4685-GMB-2017-0056
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