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Social complexity, life-history and lineage influence the molecular basis of castes in vespid wasps

A key mechanistic hypothesis for the evolution of division of labour in social insects is that a shared set of genes co-opted from a common solitary ancestral ground plan (a genetic toolkit for sociality) regulates caste differentiation across levels of social complexity. Using brain transcriptome d...

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Autores principales: Wyatt, Christopher Douglas Robert, Bentley, Michael Andrew, Taylor, Daisy, Favreau, Emeline, Brock, Ryan Edward, Taylor, Benjamin Aaron, Bell, Emily, Leadbeater, Ellouise, Sumner, Seirian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9958023/
https://www.ncbi.nlm.nih.gov/pubmed/36828829
http://dx.doi.org/10.1038/s41467-023-36456-6
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author Wyatt, Christopher Douglas Robert
Bentley, Michael Andrew
Taylor, Daisy
Favreau, Emeline
Brock, Ryan Edward
Taylor, Benjamin Aaron
Bell, Emily
Leadbeater, Ellouise
Sumner, Seirian
author_facet Wyatt, Christopher Douglas Robert
Bentley, Michael Andrew
Taylor, Daisy
Favreau, Emeline
Brock, Ryan Edward
Taylor, Benjamin Aaron
Bell, Emily
Leadbeater, Ellouise
Sumner, Seirian
author_sort Wyatt, Christopher Douglas Robert
collection PubMed
description A key mechanistic hypothesis for the evolution of division of labour in social insects is that a shared set of genes co-opted from a common solitary ancestral ground plan (a genetic toolkit for sociality) regulates caste differentiation across levels of social complexity. Using brain transcriptome data from nine species of vespid wasps, we test for overlap in differentially expressed caste genes and use machine learning models to predict castes using different gene sets. We find evidence of a shared genetic toolkit across species representing different levels of social complexity. We also find evidence of additional fine-scale differences in predictive gene sets, functional enrichment and rates of gene evolution that are related to level of social complexity, lineage and of colony founding. These results suggest that the concept of a shared genetic toolkit for sociality may be too simplistic to fully describe the process of the major transition to sociality.
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spelling pubmed-99580232023-02-26 Social complexity, life-history and lineage influence the molecular basis of castes in vespid wasps Wyatt, Christopher Douglas Robert Bentley, Michael Andrew Taylor, Daisy Favreau, Emeline Brock, Ryan Edward Taylor, Benjamin Aaron Bell, Emily Leadbeater, Ellouise Sumner, Seirian Nat Commun Article A key mechanistic hypothesis for the evolution of division of labour in social insects is that a shared set of genes co-opted from a common solitary ancestral ground plan (a genetic toolkit for sociality) regulates caste differentiation across levels of social complexity. Using brain transcriptome data from nine species of vespid wasps, we test for overlap in differentially expressed caste genes and use machine learning models to predict castes using different gene sets. We find evidence of a shared genetic toolkit across species representing different levels of social complexity. We also find evidence of additional fine-scale differences in predictive gene sets, functional enrichment and rates of gene evolution that are related to level of social complexity, lineage and of colony founding. These results suggest that the concept of a shared genetic toolkit for sociality may be too simplistic to fully describe the process of the major transition to sociality. Nature Publishing Group UK 2023-02-24 /pmc/articles/PMC9958023/ /pubmed/36828829 http://dx.doi.org/10.1038/s41467-023-36456-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wyatt, Christopher Douglas Robert
Bentley, Michael Andrew
Taylor, Daisy
Favreau, Emeline
Brock, Ryan Edward
Taylor, Benjamin Aaron
Bell, Emily
Leadbeater, Ellouise
Sumner, Seirian
Social complexity, life-history and lineage influence the molecular basis of castes in vespid wasps
title Social complexity, life-history and lineage influence the molecular basis of castes in vespid wasps
title_full Social complexity, life-history and lineage influence the molecular basis of castes in vespid wasps
title_fullStr Social complexity, life-history and lineage influence the molecular basis of castes in vespid wasps
title_full_unstemmed Social complexity, life-history and lineage influence the molecular basis of castes in vespid wasps
title_short Social complexity, life-history and lineage influence the molecular basis of castes in vespid wasps
title_sort social complexity, life-history and lineage influence the molecular basis of castes in vespid wasps
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9958023/
https://www.ncbi.nlm.nih.gov/pubmed/36828829
http://dx.doi.org/10.1038/s41467-023-36456-6
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