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Australian black field crickets show changes in neural gene expression associated with socially-induced morphological, life-history, and behavioral plasticity
BACKGROUND: Ecological and evolutionary model organisms have provided extensive insight into the ecological triggers, adaptive benefits, and evolution of life-history driven developmental plasticity. Despite this, we still have a poor understanding of the underlying genetic changes that occur during...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5078956/ https://www.ncbi.nlm.nih.gov/pubmed/27776492 http://dx.doi.org/10.1186/s12864-016-3119-y |
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author | Kasumovic, Michael M. Chen, Zhiliang Wilkins, Marc R. |
author_facet | Kasumovic, Michael M. Chen, Zhiliang Wilkins, Marc R. |
author_sort | Kasumovic, Michael M. |
collection | PubMed |
description | BACKGROUND: Ecological and evolutionary model organisms have provided extensive insight into the ecological triggers, adaptive benefits, and evolution of life-history driven developmental plasticity. Despite this, we still have a poor understanding of the underlying genetic changes that occur during shifts towards different developmental trajectories. The goal of this study is to determine whether we can identify underlying gene expression patterns that can describe the different life-history trajectories individuals follow in response to social cues of competition. To do this, we use the Australian black field cricket (Teleogryllus commodus), a species with sex-specific developmental trajectories moderated by the density and quality of calls heard during immaturity. In this study, we manipulated the social information males and females could hear by rearing individuals in either calling or silent treatments. We next used RNA-Seq to develop a reference transcriptome to study changes in brain gene expression at two points prior to sexual maturation. RESULTS: We show accelerated development in both sexes when exposed to calling; changes were also seen in growth, lifespan, and reproductive effort. Functional relationships between genes and phenotypes were apparent from ontological enrichment analysis. We demonstrate that increased investment towards traits such as growth and reproductive effort were often associated with the expression of a greater number of genes with similar effect, thus providing a suite of candidate genes for future research in this and other invertebrate organisms. CONCLUSIONS: Our results provide interesting insight into the genomic underpinnings of developmental plasticity and highlight the potential of a genomic exploration of other evolutionary theories such as condition dependence and sex-specific developmental strategies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3119-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5078956 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50789562016-10-31 Australian black field crickets show changes in neural gene expression associated with socially-induced morphological, life-history, and behavioral plasticity Kasumovic, Michael M. Chen, Zhiliang Wilkins, Marc R. BMC Genomics Research Article BACKGROUND: Ecological and evolutionary model organisms have provided extensive insight into the ecological triggers, adaptive benefits, and evolution of life-history driven developmental plasticity. Despite this, we still have a poor understanding of the underlying genetic changes that occur during shifts towards different developmental trajectories. The goal of this study is to determine whether we can identify underlying gene expression patterns that can describe the different life-history trajectories individuals follow in response to social cues of competition. To do this, we use the Australian black field cricket (Teleogryllus commodus), a species with sex-specific developmental trajectories moderated by the density and quality of calls heard during immaturity. In this study, we manipulated the social information males and females could hear by rearing individuals in either calling or silent treatments. We next used RNA-Seq to develop a reference transcriptome to study changes in brain gene expression at two points prior to sexual maturation. RESULTS: We show accelerated development in both sexes when exposed to calling; changes were also seen in growth, lifespan, and reproductive effort. Functional relationships between genes and phenotypes were apparent from ontological enrichment analysis. We demonstrate that increased investment towards traits such as growth and reproductive effort were often associated with the expression of a greater number of genes with similar effect, thus providing a suite of candidate genes for future research in this and other invertebrate organisms. CONCLUSIONS: Our results provide interesting insight into the genomic underpinnings of developmental plasticity and highlight the potential of a genomic exploration of other evolutionary theories such as condition dependence and sex-specific developmental strategies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3119-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-10-24 /pmc/articles/PMC5078956/ /pubmed/27776492 http://dx.doi.org/10.1186/s12864-016-3119-y Text en © The Author(s). 2016 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 Kasumovic, Michael M. Chen, Zhiliang Wilkins, Marc R. Australian black field crickets show changes in neural gene expression associated with socially-induced morphological, life-history, and behavioral plasticity |
title | Australian black field crickets show changes in neural gene expression associated with socially-induced morphological, life-history, and behavioral plasticity |
title_full | Australian black field crickets show changes in neural gene expression associated with socially-induced morphological, life-history, and behavioral plasticity |
title_fullStr | Australian black field crickets show changes in neural gene expression associated with socially-induced morphological, life-history, and behavioral plasticity |
title_full_unstemmed | Australian black field crickets show changes in neural gene expression associated with socially-induced morphological, life-history, and behavioral plasticity |
title_short | Australian black field crickets show changes in neural gene expression associated with socially-induced morphological, life-history, and behavioral plasticity |
title_sort | australian black field crickets show changes in neural gene expression associated with socially-induced morphological, life-history, and behavioral plasticity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5078956/ https://www.ncbi.nlm.nih.gov/pubmed/27776492 http://dx.doi.org/10.1186/s12864-016-3119-y |
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