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Relaxed selection underlies genome erosion in socially parasitic ant species
Inquiline ants are highly specialized and obligate social parasites that infiltrate and exploit colonies of closely related species. They have evolved many times convergently, are often evolutionarily young lineages, and are almost invariably rare. Focusing on the leaf-cutting ant genus Acromyrmex,...
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/PMC8131649/ https://www.ncbi.nlm.nih.gov/pubmed/34006882 http://dx.doi.org/10.1038/s41467-021-23178-w |
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author | Schrader, Lukas Pan, Hailin Bollazzi, Martin Schiøtt, Morten Larabee, Fredrick J. Bi, Xupeng Deng, Yuan Zhang, Guojie Boomsma, Jacobus J. Rabeling, Christian |
author_facet | Schrader, Lukas Pan, Hailin Bollazzi, Martin Schiøtt, Morten Larabee, Fredrick J. Bi, Xupeng Deng, Yuan Zhang, Guojie Boomsma, Jacobus J. Rabeling, Christian |
author_sort | Schrader, Lukas |
collection | PubMed |
description | Inquiline ants are highly specialized and obligate social parasites that infiltrate and exploit colonies of closely related species. They have evolved many times convergently, are often evolutionarily young lineages, and are almost invariably rare. Focusing on the leaf-cutting ant genus Acromyrmex, we compared genomes of three inquiline social parasites with their free-living, closely-related hosts. The social parasite genomes show distinct signatures of erosion compared to the host lineages, as a consequence of relaxed selective constraints on traits associated with cooperative ant colony life and of inquilines having very small effective population sizes. We find parallel gene losses, particularly in olfactory receptors, consistent with inquiline species having highly reduced social behavioral repertoires. Many of the genomic changes that we uncover resemble those observed in the genomes of obligate non-social parasites and intracellular endosymbionts that branched off into highly specialized, host-dependent niches. |
format | Online Article Text |
id | pubmed-8131649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81316492021-05-24 Relaxed selection underlies genome erosion in socially parasitic ant species Schrader, Lukas Pan, Hailin Bollazzi, Martin Schiøtt, Morten Larabee, Fredrick J. Bi, Xupeng Deng, Yuan Zhang, Guojie Boomsma, Jacobus J. Rabeling, Christian Nat Commun Article Inquiline ants are highly specialized and obligate social parasites that infiltrate and exploit colonies of closely related species. They have evolved many times convergently, are often evolutionarily young lineages, and are almost invariably rare. Focusing on the leaf-cutting ant genus Acromyrmex, we compared genomes of three inquiline social parasites with their free-living, closely-related hosts. The social parasite genomes show distinct signatures of erosion compared to the host lineages, as a consequence of relaxed selective constraints on traits associated with cooperative ant colony life and of inquilines having very small effective population sizes. We find parallel gene losses, particularly in olfactory receptors, consistent with inquiline species having highly reduced social behavioral repertoires. Many of the genomic changes that we uncover resemble those observed in the genomes of obligate non-social parasites and intracellular endosymbionts that branched off into highly specialized, host-dependent niches. Nature Publishing Group UK 2021-05-18 /pmc/articles/PMC8131649/ /pubmed/34006882 http://dx.doi.org/10.1038/s41467-021-23178-w Text en © The Author(s) 2021, corrected publication 2021 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 Schrader, Lukas Pan, Hailin Bollazzi, Martin Schiøtt, Morten Larabee, Fredrick J. Bi, Xupeng Deng, Yuan Zhang, Guojie Boomsma, Jacobus J. Rabeling, Christian Relaxed selection underlies genome erosion in socially parasitic ant species |
title | Relaxed selection underlies genome erosion in socially parasitic ant species |
title_full | Relaxed selection underlies genome erosion in socially parasitic ant species |
title_fullStr | Relaxed selection underlies genome erosion in socially parasitic ant species |
title_full_unstemmed | Relaxed selection underlies genome erosion in socially parasitic ant species |
title_short | Relaxed selection underlies genome erosion in socially parasitic ant species |
title_sort | relaxed selection underlies genome erosion in socially parasitic ant species |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8131649/ https://www.ncbi.nlm.nih.gov/pubmed/34006882 http://dx.doi.org/10.1038/s41467-021-23178-w |
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