Cargando…
Comparative transcriptomics reveals the conserved building blocks involved in parallel evolution of diverse phenotypic traits in ants
BACKGROUND: Reproductive division of labor in eusocial insects is a striking example of a shared genetic background giving rise to alternative phenotypes, namely queen and worker castes. Queen and worker phenotypes play major roles in the evolution of eusocial insects. Their behavior, morphology and...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4780134/ https://www.ncbi.nlm.nih.gov/pubmed/26951146 http://dx.doi.org/10.1186/s13059-016-0902-7 |
_version_ | 1782419723069161472 |
---|---|
author | Morandin, Claire Tin, Mandy M. Y. Abril, Sílvia Gómez, Crisanto Pontieri, Luigi Schiøtt, Morten Sundström, Liselotte Tsuji, Kazuki Pedersen, Jes Søe Helanterä, Heikki Mikheyev, Alexander S. |
author_facet | Morandin, Claire Tin, Mandy M. Y. Abril, Sílvia Gómez, Crisanto Pontieri, Luigi Schiøtt, Morten Sundström, Liselotte Tsuji, Kazuki Pedersen, Jes Søe Helanterä, Heikki Mikheyev, Alexander S. |
author_sort | Morandin, Claire |
collection | PubMed |
description | BACKGROUND: Reproductive division of labor in eusocial insects is a striking example of a shared genetic background giving rise to alternative phenotypes, namely queen and worker castes. Queen and worker phenotypes play major roles in the evolution of eusocial insects. Their behavior, morphology and physiology underpin many ecologically relevant colony-level traits, which evolved in parallel in multiple species. RESULTS: Using queen and worker transcriptomic data from 16 ant species we tested the hypothesis that conserved sets of genes are involved in ant reproductive division of labor. We further hypothesized that such sets of genes should also be involved in the parallel evolution of other key traits. We applied weighted gene co-expression network analysis, which clusters co-expressed genes into modules, whose expression levels can be summarized by their ‘eigengenes’. Eigengenes of most modules were correlated with phenotypic differentiation between queens and workers. Furthermore, eigengenes of some modules were correlated with repeated evolution of key phenotypes such as complete worker sterility, the number of queens per colony, and even invasiveness. Finally, connectivity and expression levels of genes within the co-expressed network were strongly associated with the strength of selection. Although caste-associated sets of genes evolve faster than non-caste-associated, we found no evidence for queen- or worker-associated co-expressed genes evolving faster than one another. CONCLUSIONS: These results identify conserved functionally important genomic units that likely serve as building blocks of phenotypic innovation, and allow the remarkable breadth of parallel evolution seen in ants, and possibly other eusocial insects as well. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-016-0902-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4780134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47801342016-03-08 Comparative transcriptomics reveals the conserved building blocks involved in parallel evolution of diverse phenotypic traits in ants Morandin, Claire Tin, Mandy M. Y. Abril, Sílvia Gómez, Crisanto Pontieri, Luigi Schiøtt, Morten Sundström, Liselotte Tsuji, Kazuki Pedersen, Jes Søe Helanterä, Heikki Mikheyev, Alexander S. Genome Biol Research BACKGROUND: Reproductive division of labor in eusocial insects is a striking example of a shared genetic background giving rise to alternative phenotypes, namely queen and worker castes. Queen and worker phenotypes play major roles in the evolution of eusocial insects. Their behavior, morphology and physiology underpin many ecologically relevant colony-level traits, which evolved in parallel in multiple species. RESULTS: Using queen and worker transcriptomic data from 16 ant species we tested the hypothesis that conserved sets of genes are involved in ant reproductive division of labor. We further hypothesized that such sets of genes should also be involved in the parallel evolution of other key traits. We applied weighted gene co-expression network analysis, which clusters co-expressed genes into modules, whose expression levels can be summarized by their ‘eigengenes’. Eigengenes of most modules were correlated with phenotypic differentiation between queens and workers. Furthermore, eigengenes of some modules were correlated with repeated evolution of key phenotypes such as complete worker sterility, the number of queens per colony, and even invasiveness. Finally, connectivity and expression levels of genes within the co-expressed network were strongly associated with the strength of selection. Although caste-associated sets of genes evolve faster than non-caste-associated, we found no evidence for queen- or worker-associated co-expressed genes evolving faster than one another. CONCLUSIONS: These results identify conserved functionally important genomic units that likely serve as building blocks of phenotypic innovation, and allow the remarkable breadth of parallel evolution seen in ants, and possibly other eusocial insects as well. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-016-0902-7) contains supplementary material, which is available to authorized users. BioMed Central 2016-03-07 /pmc/articles/PMC4780134/ /pubmed/26951146 http://dx.doi.org/10.1186/s13059-016-0902-7 Text en © Morandin et al. 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 Morandin, Claire Tin, Mandy M. Y. Abril, Sílvia Gómez, Crisanto Pontieri, Luigi Schiøtt, Morten Sundström, Liselotte Tsuji, Kazuki Pedersen, Jes Søe Helanterä, Heikki Mikheyev, Alexander S. Comparative transcriptomics reveals the conserved building blocks involved in parallel evolution of diverse phenotypic traits in ants |
title | Comparative transcriptomics reveals the conserved building blocks involved in parallel evolution of diverse phenotypic traits in ants |
title_full | Comparative transcriptomics reveals the conserved building blocks involved in parallel evolution of diverse phenotypic traits in ants |
title_fullStr | Comparative transcriptomics reveals the conserved building blocks involved in parallel evolution of diverse phenotypic traits in ants |
title_full_unstemmed | Comparative transcriptomics reveals the conserved building blocks involved in parallel evolution of diverse phenotypic traits in ants |
title_short | Comparative transcriptomics reveals the conserved building blocks involved in parallel evolution of diverse phenotypic traits in ants |
title_sort | comparative transcriptomics reveals the conserved building blocks involved in parallel evolution of diverse phenotypic traits in ants |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4780134/ https://www.ncbi.nlm.nih.gov/pubmed/26951146 http://dx.doi.org/10.1186/s13059-016-0902-7 |
work_keys_str_mv | AT morandinclaire comparativetranscriptomicsrevealstheconservedbuildingblocksinvolvedinparallelevolutionofdiversephenotypictraitsinants AT tinmandymy comparativetranscriptomicsrevealstheconservedbuildingblocksinvolvedinparallelevolutionofdiversephenotypictraitsinants AT abrilsilvia comparativetranscriptomicsrevealstheconservedbuildingblocksinvolvedinparallelevolutionofdiversephenotypictraitsinants AT gomezcrisanto comparativetranscriptomicsrevealstheconservedbuildingblocksinvolvedinparallelevolutionofdiversephenotypictraitsinants AT pontieriluigi comparativetranscriptomicsrevealstheconservedbuildingblocksinvolvedinparallelevolutionofdiversephenotypictraitsinants AT schiøttmorten comparativetranscriptomicsrevealstheconservedbuildingblocksinvolvedinparallelevolutionofdiversephenotypictraitsinants AT sundstromliselotte comparativetranscriptomicsrevealstheconservedbuildingblocksinvolvedinparallelevolutionofdiversephenotypictraitsinants AT tsujikazuki comparativetranscriptomicsrevealstheconservedbuildingblocksinvolvedinparallelevolutionofdiversephenotypictraitsinants AT pedersenjessøe comparativetranscriptomicsrevealstheconservedbuildingblocksinvolvedinparallelevolutionofdiversephenotypictraitsinants AT helanteraheikki comparativetranscriptomicsrevealstheconservedbuildingblocksinvolvedinparallelevolutionofdiversephenotypictraitsinants AT mikheyevalexanders comparativetranscriptomicsrevealstheconservedbuildingblocksinvolvedinparallelevolutionofdiversephenotypictraitsinants |