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Sociality sculpts similar patterns of molecular evolution in two independently evolved lineages of eusocial bees
While it is well known that the genome can affect social behavior, recent models posit that social lifestyles can, in turn, influence genome evolution. Here, we perform the most phylogenetically comprehensive comparative analysis of 16 bee genomes to date: incorporating two published and four new ca...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7977082/ https://www.ncbi.nlm.nih.gov/pubmed/33637860 http://dx.doi.org/10.1038/s42003-021-01770-6 |
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author | Shell, Wyatt A. Steffen, Michael A. Pare, Hannah K. Seetharam, Arun S. Severin, Andrew J. Toth, Amy L. Rehan, Sandra M. |
author_facet | Shell, Wyatt A. Steffen, Michael A. Pare, Hannah K. Seetharam, Arun S. Severin, Andrew J. Toth, Amy L. Rehan, Sandra M. |
author_sort | Shell, Wyatt A. |
collection | PubMed |
description | While it is well known that the genome can affect social behavior, recent models posit that social lifestyles can, in turn, influence genome evolution. Here, we perform the most phylogenetically comprehensive comparative analysis of 16 bee genomes to date: incorporating two published and four new carpenter bee genomes (Apidae: Xylocopinae) for a first-ever genomic comparison with a monophyletic clade containing solitary through advanced eusocial taxa. We find that eusocial lineages have undergone more gene family expansions, feature more signatures of positive selection, and have higher counts of taxonomically restricted genes than solitary and weakly social lineages. Transcriptomic data reveal that caste-affiliated genes are deeply-conserved; gene regulatory and functional elements are more closely tied to social phenotype than phylogenetic lineage; and regulatory complexity increases steadily with social complexity. Overall, our study provides robust empirical evidence that social evolution can act as a major and surprisingly consistent driver of macroevolutionary genomic change. |
format | Online Article Text |
id | pubmed-7977082 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79770822021-04-12 Sociality sculpts similar patterns of molecular evolution in two independently evolved lineages of eusocial bees Shell, Wyatt A. Steffen, Michael A. Pare, Hannah K. Seetharam, Arun S. Severin, Andrew J. Toth, Amy L. Rehan, Sandra M. Commun Biol Article While it is well known that the genome can affect social behavior, recent models posit that social lifestyles can, in turn, influence genome evolution. Here, we perform the most phylogenetically comprehensive comparative analysis of 16 bee genomes to date: incorporating two published and four new carpenter bee genomes (Apidae: Xylocopinae) for a first-ever genomic comparison with a monophyletic clade containing solitary through advanced eusocial taxa. We find that eusocial lineages have undergone more gene family expansions, feature more signatures of positive selection, and have higher counts of taxonomically restricted genes than solitary and weakly social lineages. Transcriptomic data reveal that caste-affiliated genes are deeply-conserved; gene regulatory and functional elements are more closely tied to social phenotype than phylogenetic lineage; and regulatory complexity increases steadily with social complexity. Overall, our study provides robust empirical evidence that social evolution can act as a major and surprisingly consistent driver of macroevolutionary genomic change. Nature Publishing Group UK 2021-02-26 /pmc/articles/PMC7977082/ /pubmed/33637860 http://dx.doi.org/10.1038/s42003-021-01770-6 Text en © The Author(s) 2021 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 Shell, Wyatt A. Steffen, Michael A. Pare, Hannah K. Seetharam, Arun S. Severin, Andrew J. Toth, Amy L. Rehan, Sandra M. Sociality sculpts similar patterns of molecular evolution in two independently evolved lineages of eusocial bees |
title | Sociality sculpts similar patterns of molecular evolution in two independently evolved lineages of eusocial bees |
title_full | Sociality sculpts similar patterns of molecular evolution in two independently evolved lineages of eusocial bees |
title_fullStr | Sociality sculpts similar patterns of molecular evolution in two independently evolved lineages of eusocial bees |
title_full_unstemmed | Sociality sculpts similar patterns of molecular evolution in two independently evolved lineages of eusocial bees |
title_short | Sociality sculpts similar patterns of molecular evolution in two independently evolved lineages of eusocial bees |
title_sort | sociality sculpts similar patterns of molecular evolution in two independently evolved lineages of eusocial bees |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7977082/ https://www.ncbi.nlm.nih.gov/pubmed/33637860 http://dx.doi.org/10.1038/s42003-021-01770-6 |
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