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A Simple Mechanism for Complex Social Behavior

The evolution of cooperation is a paradox because natural selection should favor exploitative individuals that avoid paying their fair share of any costs. Such conflict between the self-interests of cooperating individuals often results in the evolution of complex, opponent-specific, social strategi...

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Detalles Bibliográficos
Autores principales: Parkinson, Katie, Buttery, Neil J., Wolf, Jason B., Thompson, Christopher R. L.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3066132/
https://www.ncbi.nlm.nih.gov/pubmed/21468302
http://dx.doi.org/10.1371/journal.pbio.1001039
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author Parkinson, Katie
Buttery, Neil J.
Wolf, Jason B.
Thompson, Christopher R. L.
author_facet Parkinson, Katie
Buttery, Neil J.
Wolf, Jason B.
Thompson, Christopher R. L.
author_sort Parkinson, Katie
collection PubMed
description The evolution of cooperation is a paradox because natural selection should favor exploitative individuals that avoid paying their fair share of any costs. Such conflict between the self-interests of cooperating individuals often results in the evolution of complex, opponent-specific, social strategies and counterstrategies. However, the genetic and biological mechanisms underlying complex social strategies, and therefore the evolution of cooperative behavior, are largely unknown. To address this dearth of empirical data, we combine mathematical modeling, molecular genetic, and developmental approaches to test whether variation in the production of and response to social signals is sufficient to generate the complex partner-specific social success seen in the social amoeba Dictyostelium discoideum. Firstly, we find that the simple model of production of and response to social signals can generate the sort of apparent complex changes in social behavior seen in this system, without the need for partner recognition. Secondly, measurements of signal production and response in a mutant with a change in a single gene that leads to a shift in social behavior provide support for this model. Finally, these simple measurements of social signaling can also explain complex patterns of variation in social behavior generated by the natural genetic diversity found in isolates collected from the wild. Our studies therefore demonstrate a novel and elegantly simple underlying mechanistic basis for natural variation in complex social strategies in D. discoideum. More generally, they suggest that simple rules governing interactions between individuals can be sufficient to generate a diverse array of outcomes that appear complex and unpredictable when those rules are unknown.
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spelling pubmed-30661322011-04-05 A Simple Mechanism for Complex Social Behavior Parkinson, Katie Buttery, Neil J. Wolf, Jason B. Thompson, Christopher R. L. PLoS Biol Research Article The evolution of cooperation is a paradox because natural selection should favor exploitative individuals that avoid paying their fair share of any costs. Such conflict between the self-interests of cooperating individuals often results in the evolution of complex, opponent-specific, social strategies and counterstrategies. However, the genetic and biological mechanisms underlying complex social strategies, and therefore the evolution of cooperative behavior, are largely unknown. To address this dearth of empirical data, we combine mathematical modeling, molecular genetic, and developmental approaches to test whether variation in the production of and response to social signals is sufficient to generate the complex partner-specific social success seen in the social amoeba Dictyostelium discoideum. Firstly, we find that the simple model of production of and response to social signals can generate the sort of apparent complex changes in social behavior seen in this system, without the need for partner recognition. Secondly, measurements of signal production and response in a mutant with a change in a single gene that leads to a shift in social behavior provide support for this model. Finally, these simple measurements of social signaling can also explain complex patterns of variation in social behavior generated by the natural genetic diversity found in isolates collected from the wild. Our studies therefore demonstrate a novel and elegantly simple underlying mechanistic basis for natural variation in complex social strategies in D. discoideum. More generally, they suggest that simple rules governing interactions between individuals can be sufficient to generate a diverse array of outcomes that appear complex and unpredictable when those rules are unknown. Public Library of Science 2011-03-29 /pmc/articles/PMC3066132/ /pubmed/21468302 http://dx.doi.org/10.1371/journal.pbio.1001039 Text en Parkinson et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Parkinson, Katie
Buttery, Neil J.
Wolf, Jason B.
Thompson, Christopher R. L.
A Simple Mechanism for Complex Social Behavior
title A Simple Mechanism for Complex Social Behavior
title_full A Simple Mechanism for Complex Social Behavior
title_fullStr A Simple Mechanism for Complex Social Behavior
title_full_unstemmed A Simple Mechanism for Complex Social Behavior
title_short A Simple Mechanism for Complex Social Behavior
title_sort simple mechanism for complex social behavior
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3066132/
https://www.ncbi.nlm.nih.gov/pubmed/21468302
http://dx.doi.org/10.1371/journal.pbio.1001039
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