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Genome-wide effects of social status on DNA methylation in the brain of a cichlid fish, Astatotilapia burtoni
BACKGROUND: Successful social behavior requires real-time integration of information about the environment, internal physiology, and past experience. The molecular substrates of this integration are poorly understood, but likely modulate neural plasticity and gene regulation. In the cichlid fish spe...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6737626/ https://www.ncbi.nlm.nih.gov/pubmed/31506062 http://dx.doi.org/10.1186/s12864-019-6047-9 |
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author | Hilliard, Austin T. Xie, Dan Ma, Zhihai Snyder, Michael P. Fernald, Russell D. |
author_facet | Hilliard, Austin T. Xie, Dan Ma, Zhihai Snyder, Michael P. Fernald, Russell D. |
author_sort | Hilliard, Austin T. |
collection | PubMed |
description | BACKGROUND: Successful social behavior requires real-time integration of information about the environment, internal physiology, and past experience. The molecular substrates of this integration are poorly understood, but likely modulate neural plasticity and gene regulation. In the cichlid fish species Astatotilapia burtoni, male social status can shift rapidly depending on the environment, causing fast behavioral modifications and a cascade of changes in gene transcription, the brain, and the reproductive system. These changes can be permanent but are also reversible, implying the involvement of a robust but flexible mechanism that regulates plasticity based on internal and external conditions. One candidate mechanism is DNA methylation, which has been linked to social behavior in many species, including A. burtoni. But, the extent of its effects after A. burtoni social change were previously unknown. RESULTS: We performed the first genome-wide search for DNA methylation patterns associated with social status in the brains of male A. burtoni, identifying hundreds of Differentially Methylated genomic Regions (DMRs) in dominant versus non-dominant fish. Most DMRs were inside genes supporting neural development, synapse function, and other processes relevant to neural plasticity, and DMRs could affect gene expression in multiple ways. DMR genes were more likely to be transcription factors, have a duplicate elsewhere in the genome, have an anti-sense lncRNA, and have more splice variants than other genes. Dozens of genes had multiple DMRs that were often seemingly positioned to regulate specific splice variants. CONCLUSIONS: Our results revealed genome-wide effects of A. burtoni social status on DNA methylation in the brain and strongly suggest a role for methylation in modulating plasticity across multiple biological levels. They also suggest many novel hypotheses to address in mechanistic follow-up studies, and will be a rich resource for identifying the relationships between behavioral, neural, and transcriptional plasticity in the context of social status. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-019-6047-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6737626 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-67376262019-09-16 Genome-wide effects of social status on DNA methylation in the brain of a cichlid fish, Astatotilapia burtoni Hilliard, Austin T. Xie, Dan Ma, Zhihai Snyder, Michael P. Fernald, Russell D. BMC Genomics Research Article BACKGROUND: Successful social behavior requires real-time integration of information about the environment, internal physiology, and past experience. The molecular substrates of this integration are poorly understood, but likely modulate neural plasticity and gene regulation. In the cichlid fish species Astatotilapia burtoni, male social status can shift rapidly depending on the environment, causing fast behavioral modifications and a cascade of changes in gene transcription, the brain, and the reproductive system. These changes can be permanent but are also reversible, implying the involvement of a robust but flexible mechanism that regulates plasticity based on internal and external conditions. One candidate mechanism is DNA methylation, which has been linked to social behavior in many species, including A. burtoni. But, the extent of its effects after A. burtoni social change were previously unknown. RESULTS: We performed the first genome-wide search for DNA methylation patterns associated with social status in the brains of male A. burtoni, identifying hundreds of Differentially Methylated genomic Regions (DMRs) in dominant versus non-dominant fish. Most DMRs were inside genes supporting neural development, synapse function, and other processes relevant to neural plasticity, and DMRs could affect gene expression in multiple ways. DMR genes were more likely to be transcription factors, have a duplicate elsewhere in the genome, have an anti-sense lncRNA, and have more splice variants than other genes. Dozens of genes had multiple DMRs that were often seemingly positioned to regulate specific splice variants. CONCLUSIONS: Our results revealed genome-wide effects of A. burtoni social status on DNA methylation in the brain and strongly suggest a role for methylation in modulating plasticity across multiple biological levels. They also suggest many novel hypotheses to address in mechanistic follow-up studies, and will be a rich resource for identifying the relationships between behavioral, neural, and transcriptional plasticity in the context of social status. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-019-6047-9) contains supplementary material, which is available to authorized users. BioMed Central 2019-09-11 /pmc/articles/PMC6737626/ /pubmed/31506062 http://dx.doi.org/10.1186/s12864-019-6047-9 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Hilliard, Austin T. Xie, Dan Ma, Zhihai Snyder, Michael P. Fernald, Russell D. Genome-wide effects of social status on DNA methylation in the brain of a cichlid fish, Astatotilapia burtoni |
title | Genome-wide effects of social status on DNA methylation in the brain of a cichlid fish, Astatotilapia burtoni |
title_full | Genome-wide effects of social status on DNA methylation in the brain of a cichlid fish, Astatotilapia burtoni |
title_fullStr | Genome-wide effects of social status on DNA methylation in the brain of a cichlid fish, Astatotilapia burtoni |
title_full_unstemmed | Genome-wide effects of social status on DNA methylation in the brain of a cichlid fish, Astatotilapia burtoni |
title_short | Genome-wide effects of social status on DNA methylation in the brain of a cichlid fish, Astatotilapia burtoni |
title_sort | genome-wide effects of social status on dna methylation in the brain of a cichlid fish, astatotilapia burtoni |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6737626/ https://www.ncbi.nlm.nih.gov/pubmed/31506062 http://dx.doi.org/10.1186/s12864-019-6047-9 |
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