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Methyl-CpG binding domain proteins inhibit interspecies courtship and promote aggression in Drosophila
Reproductive isolation and speciation are driven by the convergence of environmental and genetic variation. The integration of these variation sources is thought to occur through epigenetic marks including DNA methylation. Proteins containing a methyl-CpG-binding domain (MBD) bind methylated DNA and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511146/ https://www.ncbi.nlm.nih.gov/pubmed/28710457 http://dx.doi.org/10.1038/s41598-017-05844-6 |
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author | Gupta, Tarun Morgan, Hannah R. Andrews, Jonathan C. Brewer, Edmond R. Certel, Sarah J. |
author_facet | Gupta, Tarun Morgan, Hannah R. Andrews, Jonathan C. Brewer, Edmond R. Certel, Sarah J. |
author_sort | Gupta, Tarun |
collection | PubMed |
description | Reproductive isolation and speciation are driven by the convergence of environmental and genetic variation. The integration of these variation sources is thought to occur through epigenetic marks including DNA methylation. Proteins containing a methyl-CpG-binding domain (MBD) bind methylated DNA and interpret epigenetic marks, providing a dynamic yet evolutionarily adapted cellular output. Here, we report the Drosophila MBD-containing proteins, dMBD-R2 and dMBD2/3, contribute to reproductive isolation and survival behavioral strategies. Drosophila melanogaster males with a reduction in dMBD-R2 specifically in octopamine (OA) neurons exhibit courtship toward divergent interspecies D. virilis and D. yakuba females and a decrease in conspecific mating success. Conspecific male-male courtship is increased between dMBD-R2-deficient males while aggression is reduced. These changes in adaptive behavior are separable as males with a hypermethylated OA neuronal genome exhibited a decrease in aggression without altering male-male courtship. These results suggest Drosophila MBD-containing proteins are required within the OA neural circuitry to inhibit interspecies and conspecific male-male courtship and indicate that the genetically hard-wired neural mechanisms enforcing behavioral reproductive isolation include the interpretation of the epigenome. |
format | Online Article Text |
id | pubmed-5511146 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55111462017-07-17 Methyl-CpG binding domain proteins inhibit interspecies courtship and promote aggression in Drosophila Gupta, Tarun Morgan, Hannah R. Andrews, Jonathan C. Brewer, Edmond R. Certel, Sarah J. Sci Rep Article Reproductive isolation and speciation are driven by the convergence of environmental and genetic variation. The integration of these variation sources is thought to occur through epigenetic marks including DNA methylation. Proteins containing a methyl-CpG-binding domain (MBD) bind methylated DNA and interpret epigenetic marks, providing a dynamic yet evolutionarily adapted cellular output. Here, we report the Drosophila MBD-containing proteins, dMBD-R2 and dMBD2/3, contribute to reproductive isolation and survival behavioral strategies. Drosophila melanogaster males with a reduction in dMBD-R2 specifically in octopamine (OA) neurons exhibit courtship toward divergent interspecies D. virilis and D. yakuba females and a decrease in conspecific mating success. Conspecific male-male courtship is increased between dMBD-R2-deficient males while aggression is reduced. These changes in adaptive behavior are separable as males with a hypermethylated OA neuronal genome exhibited a decrease in aggression without altering male-male courtship. These results suggest Drosophila MBD-containing proteins are required within the OA neural circuitry to inhibit interspecies and conspecific male-male courtship and indicate that the genetically hard-wired neural mechanisms enforcing behavioral reproductive isolation include the interpretation of the epigenome. Nature Publishing Group UK 2017-07-14 /pmc/articles/PMC5511146/ /pubmed/28710457 http://dx.doi.org/10.1038/s41598-017-05844-6 Text en © The Author(s) 2017 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Gupta, Tarun Morgan, Hannah R. Andrews, Jonathan C. Brewer, Edmond R. Certel, Sarah J. Methyl-CpG binding domain proteins inhibit interspecies courtship and promote aggression in Drosophila |
title | Methyl-CpG binding domain proteins inhibit interspecies courtship and promote aggression in Drosophila |
title_full | Methyl-CpG binding domain proteins inhibit interspecies courtship and promote aggression in Drosophila |
title_fullStr | Methyl-CpG binding domain proteins inhibit interspecies courtship and promote aggression in Drosophila |
title_full_unstemmed | Methyl-CpG binding domain proteins inhibit interspecies courtship and promote aggression in Drosophila |
title_short | Methyl-CpG binding domain proteins inhibit interspecies courtship and promote aggression in Drosophila |
title_sort | methyl-cpg binding domain proteins inhibit interspecies courtship and promote aggression in drosophila |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511146/ https://www.ncbi.nlm.nih.gov/pubmed/28710457 http://dx.doi.org/10.1038/s41598-017-05844-6 |
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