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A scaling law of multilevel evolution: how the balance between within- and among-collective evolution is determined

Numerous living systems are hierarchically organized, whereby replicating components are grouped into reproducing collectives—e.g., organelles are grouped into cells, and cells are grouped into multicellular organisms. In such systems, evolution can operate at two levels: evolution among collectives...

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Autores principales: Takeuchi, Nobuto, Mitarai, Namiko, Kaneko, Kunihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9208640/
https://www.ncbi.nlm.nih.gov/pubmed/34849893
http://dx.doi.org/10.1093/genetics/iyab182
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author Takeuchi, Nobuto
Mitarai, Namiko
Kaneko, Kunihiko
author_facet Takeuchi, Nobuto
Mitarai, Namiko
Kaneko, Kunihiko
author_sort Takeuchi, Nobuto
collection PubMed
description Numerous living systems are hierarchically organized, whereby replicating components are grouped into reproducing collectives—e.g., organelles are grouped into cells, and cells are grouped into multicellular organisms. In such systems, evolution can operate at two levels: evolution among collectives, which tends to promote selfless cooperation among components within collectives (called altruism), and evolution within collectives, which tends to promote cheating among components within collectives. The balance between within- and among-collective evolution thus exerts profound impacts on the fitness of these systems. Here, we investigate how this balance depends on the size of a collective (denoted by N) and the mutation rate of components (m) through mathematical analyses and computer simulations of multiple population genetics models. We first confirm a previous result that increasing N or m accelerates within-collective evolution relative to among-collective evolution, thus promoting the evolution of cheating. Moreover, we show that when within- and among-collective evolution exactly balance each other out, the following scaling relation generally holds: [Formula: see text] is a constant, where scaling exponent α depends on multiple parameters, such as the strength of selection and whether altruism is a binary or quantitative trait. This relation indicates that although N and m have quantitatively distinct impacts on the balance between within- and among-collective evolution, their impacts become identical if m is scaled with a proper exponent. Our results thus provide a novel insight into conditions under which cheating or altruism evolves in hierarchically organized replicating systems.
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spelling pubmed-92086402022-06-21 A scaling law of multilevel evolution: how the balance between within- and among-collective evolution is determined Takeuchi, Nobuto Mitarai, Namiko Kaneko, Kunihiko Genetics Investigation Numerous living systems are hierarchically organized, whereby replicating components are grouped into reproducing collectives—e.g., organelles are grouped into cells, and cells are grouped into multicellular organisms. In such systems, evolution can operate at two levels: evolution among collectives, which tends to promote selfless cooperation among components within collectives (called altruism), and evolution within collectives, which tends to promote cheating among components within collectives. The balance between within- and among-collective evolution thus exerts profound impacts on the fitness of these systems. Here, we investigate how this balance depends on the size of a collective (denoted by N) and the mutation rate of components (m) through mathematical analyses and computer simulations of multiple population genetics models. We first confirm a previous result that increasing N or m accelerates within-collective evolution relative to among-collective evolution, thus promoting the evolution of cheating. Moreover, we show that when within- and among-collective evolution exactly balance each other out, the following scaling relation generally holds: [Formula: see text] is a constant, where scaling exponent α depends on multiple parameters, such as the strength of selection and whether altruism is a binary or quantitative trait. This relation indicates that although N and m have quantitatively distinct impacts on the balance between within- and among-collective evolution, their impacts become identical if m is scaled with a proper exponent. Our results thus provide a novel insight into conditions under which cheating or altruism evolves in hierarchically organized replicating systems. Oxford University Press 2021-10-23 /pmc/articles/PMC9208640/ /pubmed/34849893 http://dx.doi.org/10.1093/genetics/iyab182 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Genetics Society of America. 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 Investigation
Takeuchi, Nobuto
Mitarai, Namiko
Kaneko, Kunihiko
A scaling law of multilevel evolution: how the balance between within- and among-collective evolution is determined
title A scaling law of multilevel evolution: how the balance between within- and among-collective evolution is determined
title_full A scaling law of multilevel evolution: how the balance between within- and among-collective evolution is determined
title_fullStr A scaling law of multilevel evolution: how the balance between within- and among-collective evolution is determined
title_full_unstemmed A scaling law of multilevel evolution: how the balance between within- and among-collective evolution is determined
title_short A scaling law of multilevel evolution: how the balance between within- and among-collective evolution is determined
title_sort scaling law of multilevel evolution: how the balance between within- and among-collective evolution is determined
topic Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9208640/
https://www.ncbi.nlm.nih.gov/pubmed/34849893
http://dx.doi.org/10.1093/genetics/iyab182
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