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A unified framework for measuring selection on cellular lineages and traits

Intracellular states probed by gene expression profiles and metabolic activities are intrinsically noisy, causing phenotypic variations among cellular lineages. Understanding the adaptive and evolutionary roles of such variations requires clarifying their linkage to population growth rates. Extendin...

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Autores principales: Yamauchi, Shunpei, Nozoe, Takashi, Okura, Reiko, Kussell, Edo, Wakamoto, Yuichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9725751/
https://www.ncbi.nlm.nih.gov/pubmed/36472074
http://dx.doi.org/10.7554/eLife.72299
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author Yamauchi, Shunpei
Nozoe, Takashi
Okura, Reiko
Kussell, Edo
Wakamoto, Yuichi
author_facet Yamauchi, Shunpei
Nozoe, Takashi
Okura, Reiko
Kussell, Edo
Wakamoto, Yuichi
author_sort Yamauchi, Shunpei
collection PubMed
description Intracellular states probed by gene expression profiles and metabolic activities are intrinsically noisy, causing phenotypic variations among cellular lineages. Understanding the adaptive and evolutionary roles of such variations requires clarifying their linkage to population growth rates. Extending a cell lineage statistics framework, here we show that a population’s growth rate can be expanded by the cumulants of a fitness landscape that characterize how fitness distributes in a population. The expansion enables quantifying the contribution of each cumulant, such as variance and skewness, to population growth. We introduce a function that contains all the essential information of cell lineage statistics, including mean lineage fitness and selection strength. We reveal a relation between fitness heterogeneity and population growth rate response to perturbation. We apply the framework to experimental cell lineage data from bacteria to mammalian cells, revealing distinct levels of growth rate gain from fitness heterogeneity across environments and organisms. Furthermore, third or higher order cumulants’ contributions are negligible under constant growth conditions but could be significant in regrowing processes from growth-arrested conditions. We identify cellular populations in which selection leads to an increase of fitness variance among lineages in retrospective statistics compared to chronological statistics. The framework assumes no particular growth models or environmental conditions, and is thus applicable to various biological phenomena for which phenotypic heterogeneity and cellular proliferation are important.
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spelling pubmed-97257512022-12-07 A unified framework for measuring selection on cellular lineages and traits Yamauchi, Shunpei Nozoe, Takashi Okura, Reiko Kussell, Edo Wakamoto, Yuichi eLife Computational and Systems Biology Intracellular states probed by gene expression profiles and metabolic activities are intrinsically noisy, causing phenotypic variations among cellular lineages. Understanding the adaptive and evolutionary roles of such variations requires clarifying their linkage to population growth rates. Extending a cell lineage statistics framework, here we show that a population’s growth rate can be expanded by the cumulants of a fitness landscape that characterize how fitness distributes in a population. The expansion enables quantifying the contribution of each cumulant, such as variance and skewness, to population growth. We introduce a function that contains all the essential information of cell lineage statistics, including mean lineage fitness and selection strength. We reveal a relation between fitness heterogeneity and population growth rate response to perturbation. We apply the framework to experimental cell lineage data from bacteria to mammalian cells, revealing distinct levels of growth rate gain from fitness heterogeneity across environments and organisms. Furthermore, third or higher order cumulants’ contributions are negligible under constant growth conditions but could be significant in regrowing processes from growth-arrested conditions. We identify cellular populations in which selection leads to an increase of fitness variance among lineages in retrospective statistics compared to chronological statistics. The framework assumes no particular growth models or environmental conditions, and is thus applicable to various biological phenomena for which phenotypic heterogeneity and cellular proliferation are important. eLife Sciences Publications, Ltd 2022-12-06 /pmc/articles/PMC9725751/ /pubmed/36472074 http://dx.doi.org/10.7554/eLife.72299 Text en © 2022, Yamauchi et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Computational and Systems Biology
Yamauchi, Shunpei
Nozoe, Takashi
Okura, Reiko
Kussell, Edo
Wakamoto, Yuichi
A unified framework for measuring selection on cellular lineages and traits
title A unified framework for measuring selection on cellular lineages and traits
title_full A unified framework for measuring selection on cellular lineages and traits
title_fullStr A unified framework for measuring selection on cellular lineages and traits
title_full_unstemmed A unified framework for measuring selection on cellular lineages and traits
title_short A unified framework for measuring selection on cellular lineages and traits
title_sort unified framework for measuring selection on cellular lineages and traits
topic Computational and Systems Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9725751/
https://www.ncbi.nlm.nih.gov/pubmed/36472074
http://dx.doi.org/10.7554/eLife.72299
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