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Clonality and non-linearity drive facultative-cooperation allele diversity
Kin discrimination describes the differential interaction of organisms with kin versus non-kin. In microorganisms, many genetic loci act as effective kin-discrimination systems, such as kin-directed help and non-kin-directed harm. Another important example is facultative cooperation, where cooperato...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6461992/ https://www.ncbi.nlm.nih.gov/pubmed/30464316 http://dx.doi.org/10.1038/s41396-018-0310-y |
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author | Ben-Zion, Ishay Pollak, Shaul Eldar, Avigdor |
author_facet | Ben-Zion, Ishay Pollak, Shaul Eldar, Avigdor |
author_sort | Ben-Zion, Ishay |
collection | PubMed |
description | Kin discrimination describes the differential interaction of organisms with kin versus non-kin. In microorganisms, many genetic loci act as effective kin-discrimination systems, such as kin-directed help and non-kin-directed harm. Another important example is facultative cooperation, where cooperators increase their investment in group-directed cooperation with the abundance of their kin in the group. Many of these kin-discrimination loci are highly diversified, yet it remains unclear what evolutionary mechanisms maintain this diversity, and how it is affected by population structure. Here, we demonstrate the unique dependence of kin-discriminative interactions on population structure, and how this could explain facultative-cooperation allele-diversity. We show mathematically that low relatedness between microbes in non-clonal social groups is needed to maintain the diversity of facultative-cooperation alleles, while high clonality is needed to stabilize this diversity against cheating. Interestingly, we demonstrate with simulations that such population structure occurs naturally in expanding microbial colonies. Finally, analysis of experimental data of quorum-sensing mediated facultative cooperation, in Bacillus subtilis, demonstrates the relevance of our results to realistic microbial interactions, due to their intrinsic non-linear frequency dependence. Our analysis therefore stresses the impact of clonality on the interplay between exploitation and kin discrimination and portrays a way for the evolution of facultative cooperation. |
format | Online Article Text |
id | pubmed-6461992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64619922019-10-04 Clonality and non-linearity drive facultative-cooperation allele diversity Ben-Zion, Ishay Pollak, Shaul Eldar, Avigdor ISME J Article Kin discrimination describes the differential interaction of organisms with kin versus non-kin. In microorganisms, many genetic loci act as effective kin-discrimination systems, such as kin-directed help and non-kin-directed harm. Another important example is facultative cooperation, where cooperators increase their investment in group-directed cooperation with the abundance of their kin in the group. Many of these kin-discrimination loci are highly diversified, yet it remains unclear what evolutionary mechanisms maintain this diversity, and how it is affected by population structure. Here, we demonstrate the unique dependence of kin-discriminative interactions on population structure, and how this could explain facultative-cooperation allele-diversity. We show mathematically that low relatedness between microbes in non-clonal social groups is needed to maintain the diversity of facultative-cooperation alleles, while high clonality is needed to stabilize this diversity against cheating. Interestingly, we demonstrate with simulations that such population structure occurs naturally in expanding microbial colonies. Finally, analysis of experimental data of quorum-sensing mediated facultative cooperation, in Bacillus subtilis, demonstrates the relevance of our results to realistic microbial interactions, due to their intrinsic non-linear frequency dependence. Our analysis therefore stresses the impact of clonality on the interplay between exploitation and kin discrimination and portrays a way for the evolution of facultative cooperation. Nature Publishing Group UK 2018-11-21 2019-03 /pmc/articles/PMC6461992/ /pubmed/30464316 http://dx.doi.org/10.1038/s41396-018-0310-y Text en © The Author(s) 2018 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 Ben-Zion, Ishay Pollak, Shaul Eldar, Avigdor Clonality and non-linearity drive facultative-cooperation allele diversity |
title | Clonality and non-linearity drive facultative-cooperation allele diversity |
title_full | Clonality and non-linearity drive facultative-cooperation allele diversity |
title_fullStr | Clonality and non-linearity drive facultative-cooperation allele diversity |
title_full_unstemmed | Clonality and non-linearity drive facultative-cooperation allele diversity |
title_short | Clonality and non-linearity drive facultative-cooperation allele diversity |
title_sort | clonality and non-linearity drive facultative-cooperation allele diversity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6461992/ https://www.ncbi.nlm.nih.gov/pubmed/30464316 http://dx.doi.org/10.1038/s41396-018-0310-y |
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