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Molecular evolution of DNMT1 in vertebrates: Duplications in marsupials followed by positive selection

DNA methylation is mediated by a conserved family of DNA methyltransferases (Dnmts). The human genome encodes three active Dnmts (Dnmt1, Dnmt3a and Dnmt3b), the tRNA methyltransferase Dnmt2, and the regulatory protein Dnmt3L. Despite their high degree of conservation among different species, genes e...

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Autores principales: Alvarez-Ponce, David, Torres-Sánchez, María, Feyertag, Felix, Kulkarni, Asmita, Nappi, Taylen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5886458/
https://www.ncbi.nlm.nih.gov/pubmed/29621315
http://dx.doi.org/10.1371/journal.pone.0195162
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author Alvarez-Ponce, David
Torres-Sánchez, María
Feyertag, Felix
Kulkarni, Asmita
Nappi, Taylen
author_facet Alvarez-Ponce, David
Torres-Sánchez, María
Feyertag, Felix
Kulkarni, Asmita
Nappi, Taylen
author_sort Alvarez-Ponce, David
collection PubMed
description DNA methylation is mediated by a conserved family of DNA methyltransferases (Dnmts). The human genome encodes three active Dnmts (Dnmt1, Dnmt3a and Dnmt3b), the tRNA methyltransferase Dnmt2, and the regulatory protein Dnmt3L. Despite their high degree of conservation among different species, genes encoding Dnmts have been duplicated and/or lost in multiple lineages throughout evolution, indicating that the DNA methylation machinery has some potential to undergo evolutionary change. However, little is known about the extent to which this machinery, or the methylome, varies among vertebrates. Here, we study the molecular evolution of Dnmt1, the enzyme responsible for maintenance of DNA methylation patterns after replication, in 79 vertebrate species. Our analyses show that all studied species exhibit a single copy of the DNMT1 gene, with the exception of tilapia and marsupials (tammar wallaby, koala, Tasmanian devil and opossum), each of which displays two apparently functional DNMT1 copies. Our phylogenetic analyses indicate that DNMT1 duplicated before the radiation of major marsupial groups (i.e., at least ~75 million years ago), thus giving rise to two DNMT1 copies in marsupials (copy 1 and copy 2). In the opossum lineage, copy 2 was lost, and copy 1 recently duplicated again, generating three DNMT1 copies: two putatively functional genes (copy 1a and 1b) and one pseudogene (copy 1ψ). Both marsupial copies (DNMT1 copies 1 and 2) are under purifying selection, and copy 2 exhibits elevated rates of evolution and signatures of positive selection, suggesting a scenario of neofunctionalization. This gene duplication might have resulted in modifications in marsupial methylomes and their dynamics.
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spelling pubmed-58864582018-04-20 Molecular evolution of DNMT1 in vertebrates: Duplications in marsupials followed by positive selection Alvarez-Ponce, David Torres-Sánchez, María Feyertag, Felix Kulkarni, Asmita Nappi, Taylen PLoS One Research Article DNA methylation is mediated by a conserved family of DNA methyltransferases (Dnmts). The human genome encodes three active Dnmts (Dnmt1, Dnmt3a and Dnmt3b), the tRNA methyltransferase Dnmt2, and the regulatory protein Dnmt3L. Despite their high degree of conservation among different species, genes encoding Dnmts have been duplicated and/or lost in multiple lineages throughout evolution, indicating that the DNA methylation machinery has some potential to undergo evolutionary change. However, little is known about the extent to which this machinery, or the methylome, varies among vertebrates. Here, we study the molecular evolution of Dnmt1, the enzyme responsible for maintenance of DNA methylation patterns after replication, in 79 vertebrate species. Our analyses show that all studied species exhibit a single copy of the DNMT1 gene, with the exception of tilapia and marsupials (tammar wallaby, koala, Tasmanian devil and opossum), each of which displays two apparently functional DNMT1 copies. Our phylogenetic analyses indicate that DNMT1 duplicated before the radiation of major marsupial groups (i.e., at least ~75 million years ago), thus giving rise to two DNMT1 copies in marsupials (copy 1 and copy 2). In the opossum lineage, copy 2 was lost, and copy 1 recently duplicated again, generating three DNMT1 copies: two putatively functional genes (copy 1a and 1b) and one pseudogene (copy 1ψ). Both marsupial copies (DNMT1 copies 1 and 2) are under purifying selection, and copy 2 exhibits elevated rates of evolution and signatures of positive selection, suggesting a scenario of neofunctionalization. This gene duplication might have resulted in modifications in marsupial methylomes and their dynamics. Public Library of Science 2018-04-05 /pmc/articles/PMC5886458/ /pubmed/29621315 http://dx.doi.org/10.1371/journal.pone.0195162 Text en © 2018 Alvarez-Ponce et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Alvarez-Ponce, David
Torres-Sánchez, María
Feyertag, Felix
Kulkarni, Asmita
Nappi, Taylen
Molecular evolution of DNMT1 in vertebrates: Duplications in marsupials followed by positive selection
title Molecular evolution of DNMT1 in vertebrates: Duplications in marsupials followed by positive selection
title_full Molecular evolution of DNMT1 in vertebrates: Duplications in marsupials followed by positive selection
title_fullStr Molecular evolution of DNMT1 in vertebrates: Duplications in marsupials followed by positive selection
title_full_unstemmed Molecular evolution of DNMT1 in vertebrates: Duplications in marsupials followed by positive selection
title_short Molecular evolution of DNMT1 in vertebrates: Duplications in marsupials followed by positive selection
title_sort molecular evolution of dnmt1 in vertebrates: duplications in marsupials followed by positive selection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5886458/
https://www.ncbi.nlm.nih.gov/pubmed/29621315
http://dx.doi.org/10.1371/journal.pone.0195162
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