Cargando…

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,...

Descripción completa

Detalles Bibliográficos
Autores principales: Schrader, Lukas, Pan, Hailin, Bollazzi, Martin, Schiøtt, Morten, Larabee, Fredrick J., Bi, Xupeng, Deng, Yuan, Zhang, Guojie, Boomsma, Jacobus J., Rabeling, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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
_version_ 1783694744402001920
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
work_keys_str_mv AT schraderlukas relaxedselectionunderliesgenomeerosioninsociallyparasiticantspecies
AT panhailin relaxedselectionunderliesgenomeerosioninsociallyparasiticantspecies
AT bollazzimartin relaxedselectionunderliesgenomeerosioninsociallyparasiticantspecies
AT schiøttmorten relaxedselectionunderliesgenomeerosioninsociallyparasiticantspecies
AT larabeefredrickj relaxedselectionunderliesgenomeerosioninsociallyparasiticantspecies
AT bixupeng relaxedselectionunderliesgenomeerosioninsociallyparasiticantspecies
AT dengyuan relaxedselectionunderliesgenomeerosioninsociallyparasiticantspecies
AT zhangguojie relaxedselectionunderliesgenomeerosioninsociallyparasiticantspecies
AT boomsmajacobusj relaxedselectionunderliesgenomeerosioninsociallyparasiticantspecies
AT rabelingchristian relaxedselectionunderliesgenomeerosioninsociallyparasiticantspecies