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Pleiotropy alleviates the fitness costs associated with resource allocation trade-offs in immune signaling networks

Many genes and signaling pathways within plant and animal taxa drive the expression of multiple organismal traits. This form of genetic pleiotropy instigates trade-offs among life-history traits if a mutation in the pleiotropic gene improves the fitness contribution of one trait at the expense of an...

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Autores principales: Martin, Reese, Tate, Ann.T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10592669/
https://www.ncbi.nlm.nih.gov/pubmed/37873469
http://dx.doi.org/10.1101/2023.10.06.561276
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author Martin, Reese
Tate, Ann.T.
author_facet Martin, Reese
Tate, Ann.T.
author_sort Martin, Reese
collection PubMed
description Many genes and signaling pathways within plant and animal taxa drive the expression of multiple organismal traits. This form of genetic pleiotropy instigates trade-offs among life-history traits if a mutation in the pleiotropic gene improves the fitness contribution of one trait at the expense of another. Whether or not pleiotropy gives rise to conflict among traits, however, likely depends on the resource costs and timing of trait deployment during organismal development. To investigate factors that could influence the evolutionary maintenance of pleiotropy in gene networks, we developed an agent-based model of co-evolution between parasites and hosts. Hosts comprise signaling networks that must faithfully complete a developmental program while also defending against parasites, and trait signaling networks could be independent or share a pleiotropic component as they evolved to improve host fitness. We found that hosts with independent developmental and immune networks were significantly more fit than hosts with pleiotropic networks when traits were deployed asynchronously during development. When host genotypes directly competed against each other, however, pleiotropic hosts were victorious regardless of trait synchrony because the pleiotropic networks were more robust to parasite manipulation, potentially explaining the abundance of pleiotropy in immune systems despite its contribution to life history trade-offs.
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spelling pubmed-105926692023-10-24 Pleiotropy alleviates the fitness costs associated with resource allocation trade-offs in immune signaling networks Martin, Reese Tate, Ann.T. bioRxiv Article Many genes and signaling pathways within plant and animal taxa drive the expression of multiple organismal traits. This form of genetic pleiotropy instigates trade-offs among life-history traits if a mutation in the pleiotropic gene improves the fitness contribution of one trait at the expense of another. Whether or not pleiotropy gives rise to conflict among traits, however, likely depends on the resource costs and timing of trait deployment during organismal development. To investigate factors that could influence the evolutionary maintenance of pleiotropy in gene networks, we developed an agent-based model of co-evolution between parasites and hosts. Hosts comprise signaling networks that must faithfully complete a developmental program while also defending against parasites, and trait signaling networks could be independent or share a pleiotropic component as they evolved to improve host fitness. We found that hosts with independent developmental and immune networks were significantly more fit than hosts with pleiotropic networks when traits were deployed asynchronously during development. When host genotypes directly competed against each other, however, pleiotropic hosts were victorious regardless of trait synchrony because the pleiotropic networks were more robust to parasite manipulation, potentially explaining the abundance of pleiotropy in immune systems despite its contribution to life history trade-offs. Cold Spring Harbor Laboratory 2023-10-10 /pmc/articles/PMC10592669/ /pubmed/37873469 http://dx.doi.org/10.1101/2023.10.06.561276 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Martin, Reese
Tate, Ann.T.
Pleiotropy alleviates the fitness costs associated with resource allocation trade-offs in immune signaling networks
title Pleiotropy alleviates the fitness costs associated with resource allocation trade-offs in immune signaling networks
title_full Pleiotropy alleviates the fitness costs associated with resource allocation trade-offs in immune signaling networks
title_fullStr Pleiotropy alleviates the fitness costs associated with resource allocation trade-offs in immune signaling networks
title_full_unstemmed Pleiotropy alleviates the fitness costs associated with resource allocation trade-offs in immune signaling networks
title_short Pleiotropy alleviates the fitness costs associated with resource allocation trade-offs in immune signaling networks
title_sort pleiotropy alleviates the fitness costs associated with resource allocation trade-offs in immune signaling networks
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10592669/
https://www.ncbi.nlm.nih.gov/pubmed/37873469
http://dx.doi.org/10.1101/2023.10.06.561276
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