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Comprehensive DNA methylation analysis of the Aedes aegypti genome

Aedes aegypti mosquitoes are important vectors of viral diseases. Mosquito host factors play key roles in virus control and it has been suggested that dengue virus replication is regulated by Dnmt2-mediated DNA methylation. However, recent studies have shown that Dnmt2 is a tRNA methyltransferase an...

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Autores principales: Falckenhayn, Cassandra, Carneiro, Vitor Coutinho, de Mendonça Amarante, Anderson, Schmid, Katharina, Hanna, Katharina, Kang, Seokyoung, Helm, Mark, Dimopoulos, George, Fantappié, Marcelo Rosado, Lyko, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5090363/
https://www.ncbi.nlm.nih.gov/pubmed/27805064
http://dx.doi.org/10.1038/srep36444
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author Falckenhayn, Cassandra
Carneiro, Vitor Coutinho
de Mendonça Amarante, Anderson
Schmid, Katharina
Hanna, Katharina
Kang, Seokyoung
Helm, Mark
Dimopoulos, George
Fantappié, Marcelo Rosado
Lyko, Frank
author_facet Falckenhayn, Cassandra
Carneiro, Vitor Coutinho
de Mendonça Amarante, Anderson
Schmid, Katharina
Hanna, Katharina
Kang, Seokyoung
Helm, Mark
Dimopoulos, George
Fantappié, Marcelo Rosado
Lyko, Frank
author_sort Falckenhayn, Cassandra
collection PubMed
description Aedes aegypti mosquitoes are important vectors of viral diseases. Mosquito host factors play key roles in virus control and it has been suggested that dengue virus replication is regulated by Dnmt2-mediated DNA methylation. However, recent studies have shown that Dnmt2 is a tRNA methyltransferase and that Dnmt2-dependent methylomes lack defined DNA methylation patterns, thus necessitating a systematic re-evaluation of the mosquito genome methylation status. We have now searched the Ae. aegypti genome for candidate DNA modification enzymes. This failed to reveal any known (cytosine-5) DNA methyltransferases, but identified homologues for the Dnmt2 tRNA methyltransferase, the Mettl4 (adenine-6) DNA methyltransferase, and the Tet DNA demethylase. All genes were expressed at variable levels throughout mosquito development. Mass spectrometry demonstrated that DNA methylation levels were several orders of magnitude below the levels that are usually detected in organisms with DNA methylation-dependent epigenetic regulation. Furthermore, whole-genome bisulfite sequencing failed to reveal any evidence of defined DNA methylation patterns. These results suggest that the Ae. aegypti genome is unmethylated. Interestingly, additional RNA bisulfite sequencing provided first evidence for Dnmt2-mediated tRNA methylation in mosquitoes. These findings have important implications for understanding the mechanism of Dnmt2-dependent virus regulation.
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spelling pubmed-50903632016-11-08 Comprehensive DNA methylation analysis of the Aedes aegypti genome Falckenhayn, Cassandra Carneiro, Vitor Coutinho de Mendonça Amarante, Anderson Schmid, Katharina Hanna, Katharina Kang, Seokyoung Helm, Mark Dimopoulos, George Fantappié, Marcelo Rosado Lyko, Frank Sci Rep Article Aedes aegypti mosquitoes are important vectors of viral diseases. Mosquito host factors play key roles in virus control and it has been suggested that dengue virus replication is regulated by Dnmt2-mediated DNA methylation. However, recent studies have shown that Dnmt2 is a tRNA methyltransferase and that Dnmt2-dependent methylomes lack defined DNA methylation patterns, thus necessitating a systematic re-evaluation of the mosquito genome methylation status. We have now searched the Ae. aegypti genome for candidate DNA modification enzymes. This failed to reveal any known (cytosine-5) DNA methyltransferases, but identified homologues for the Dnmt2 tRNA methyltransferase, the Mettl4 (adenine-6) DNA methyltransferase, and the Tet DNA demethylase. All genes were expressed at variable levels throughout mosquito development. Mass spectrometry demonstrated that DNA methylation levels were several orders of magnitude below the levels that are usually detected in organisms with DNA methylation-dependent epigenetic regulation. Furthermore, whole-genome bisulfite sequencing failed to reveal any evidence of defined DNA methylation patterns. These results suggest that the Ae. aegypti genome is unmethylated. Interestingly, additional RNA bisulfite sequencing provided first evidence for Dnmt2-mediated tRNA methylation in mosquitoes. These findings have important implications for understanding the mechanism of Dnmt2-dependent virus regulation. Nature Publishing Group 2016-11-02 /pmc/articles/PMC5090363/ /pubmed/27805064 http://dx.doi.org/10.1038/srep36444 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Falckenhayn, Cassandra
Carneiro, Vitor Coutinho
de Mendonça Amarante, Anderson
Schmid, Katharina
Hanna, Katharina
Kang, Seokyoung
Helm, Mark
Dimopoulos, George
Fantappié, Marcelo Rosado
Lyko, Frank
Comprehensive DNA methylation analysis of the Aedes aegypti genome
title Comprehensive DNA methylation analysis of the Aedes aegypti genome
title_full Comprehensive DNA methylation analysis of the Aedes aegypti genome
title_fullStr Comprehensive DNA methylation analysis of the Aedes aegypti genome
title_full_unstemmed Comprehensive DNA methylation analysis of the Aedes aegypti genome
title_short Comprehensive DNA methylation analysis of the Aedes aegypti genome
title_sort comprehensive dna methylation analysis of the aedes aegypti genome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5090363/
https://www.ncbi.nlm.nih.gov/pubmed/27805064
http://dx.doi.org/10.1038/srep36444
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