Cargando…
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...
Autores principales: | , , , , |
---|---|
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 |
_version_ | 1784844634465239040 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9725751 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT yamauchishunpei aunifiedframeworkformeasuringselectiononcellularlineagesandtraits AT nozoetakashi aunifiedframeworkformeasuringselectiononcellularlineagesandtraits AT okurareiko aunifiedframeworkformeasuringselectiononcellularlineagesandtraits AT kusselledo aunifiedframeworkformeasuringselectiononcellularlineagesandtraits AT wakamotoyuichi aunifiedframeworkformeasuringselectiononcellularlineagesandtraits AT yamauchishunpei unifiedframeworkformeasuringselectiononcellularlineagesandtraits AT nozoetakashi unifiedframeworkformeasuringselectiononcellularlineagesandtraits AT okurareiko unifiedframeworkformeasuringselectiononcellularlineagesandtraits AT kusselledo unifiedframeworkformeasuringselectiononcellularlineagesandtraits AT wakamotoyuichi unifiedframeworkformeasuringselectiononcellularlineagesandtraits |