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Convergent Loss of Chemoreceptors across Independent Origins of Slave-Making in Ants
The evolution of an obligate parasitic lifestyle often leads to the reduction of morphological and physiological traits, which may be accompanied by loss of genes and functions. Slave-making ants are social parasites that exploit the work force of closely related ant species for social behaviors suc...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8760941/ https://www.ncbi.nlm.nih.gov/pubmed/34668533 http://dx.doi.org/10.1093/molbev/msab305 |
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author | Jongepier, Evelien Séguret, Alice Labutin, Anton Feldmeyer, Barbara Gstöttl, Claudia Foitzik, Susanne Heinze, Jürgen Bornberg-Bauer, Erich |
author_facet | Jongepier, Evelien Séguret, Alice Labutin, Anton Feldmeyer, Barbara Gstöttl, Claudia Foitzik, Susanne Heinze, Jürgen Bornberg-Bauer, Erich |
author_sort | Jongepier, Evelien |
collection | PubMed |
description | The evolution of an obligate parasitic lifestyle often leads to the reduction of morphological and physiological traits, which may be accompanied by loss of genes and functions. Slave-making ants are social parasites that exploit the work force of closely related ant species for social behaviors such as brood care and foraging. Recent divergence between these social parasites and their hosts enables comparative studies of gene family evolution. We sequenced the genomes of eight ant species, representing three independent origins of ant slavery. During the evolution of eusociality, chemoreceptor genes multiplied due to the importance of chemical communication in insect societies. We investigated the evolutionary fate of these chemoreceptors and found that slave-making ant genomes harbored only half as many gustatory receptors as their hosts’, potentially mirroring the outsourcing of foraging tasks to host workers. In addition, parasites had fewer odorant receptors and their loss shows striking patterns of convergence across independent origins of parasitism, in particular in orthologs often implicated in sociality like the 9-exon odorant receptors. These convergent losses represent a rare case of convergent molecular evolution at the level of individual genes. Thus, evolution can operate in a way that is both repeatable and reversible when independent ant lineages lose important social traits during the transition to a parasitic lifestyle. |
format | Online Article Text |
id | pubmed-8760941 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-87609412022-01-18 Convergent Loss of Chemoreceptors across Independent Origins of Slave-Making in Ants Jongepier, Evelien Séguret, Alice Labutin, Anton Feldmeyer, Barbara Gstöttl, Claudia Foitzik, Susanne Heinze, Jürgen Bornberg-Bauer, Erich Mol Biol Evol Discoveries The evolution of an obligate parasitic lifestyle often leads to the reduction of morphological and physiological traits, which may be accompanied by loss of genes and functions. Slave-making ants are social parasites that exploit the work force of closely related ant species for social behaviors such as brood care and foraging. Recent divergence between these social parasites and their hosts enables comparative studies of gene family evolution. We sequenced the genomes of eight ant species, representing three independent origins of ant slavery. During the evolution of eusociality, chemoreceptor genes multiplied due to the importance of chemical communication in insect societies. We investigated the evolutionary fate of these chemoreceptors and found that slave-making ant genomes harbored only half as many gustatory receptors as their hosts’, potentially mirroring the outsourcing of foraging tasks to host workers. In addition, parasites had fewer odorant receptors and their loss shows striking patterns of convergence across independent origins of parasitism, in particular in orthologs often implicated in sociality like the 9-exon odorant receptors. These convergent losses represent a rare case of convergent molecular evolution at the level of individual genes. Thus, evolution can operate in a way that is both repeatable and reversible when independent ant lineages lose important social traits during the transition to a parasitic lifestyle. Oxford University Press 2021-10-20 /pmc/articles/PMC8760941/ /pubmed/34668533 http://dx.doi.org/10.1093/molbev/msab305 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Discoveries Jongepier, Evelien Séguret, Alice Labutin, Anton Feldmeyer, Barbara Gstöttl, Claudia Foitzik, Susanne Heinze, Jürgen Bornberg-Bauer, Erich Convergent Loss of Chemoreceptors across Independent Origins of Slave-Making in Ants |
title | Convergent Loss of Chemoreceptors across Independent Origins of Slave-Making in Ants |
title_full | Convergent Loss of Chemoreceptors across Independent Origins of Slave-Making in Ants |
title_fullStr | Convergent Loss of Chemoreceptors across Independent Origins of Slave-Making in Ants |
title_full_unstemmed | Convergent Loss of Chemoreceptors across Independent Origins of Slave-Making in Ants |
title_short | Convergent Loss of Chemoreceptors across Independent Origins of Slave-Making in Ants |
title_sort | convergent loss of chemoreceptors across independent origins of slave-making in ants |
topic | Discoveries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8760941/ https://www.ncbi.nlm.nih.gov/pubmed/34668533 http://dx.doi.org/10.1093/molbev/msab305 |
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