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The effect of mutational robustness on the evolvability of multicellular organisms and eukaryotic cells
Canalization involves mutational robustness, the lack of phenotypic change as a result of genetic mutations. Given the large divergence in phenotype across species, understanding the relationship between high robustness and evolvability has been of interest to both theorists and experimentalists. Al...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315174/ https://www.ncbi.nlm.nih.gov/pubmed/37256290 http://dx.doi.org/10.1111/jeb.14180 |
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author | Jiang, Pengyao Kreitman, Martin Reinitz, John |
author_facet | Jiang, Pengyao Kreitman, Martin Reinitz, John |
author_sort | Jiang, Pengyao |
collection | PubMed |
description | Canalization involves mutational robustness, the lack of phenotypic change as a result of genetic mutations. Given the large divergence in phenotype across species, understanding the relationship between high robustness and evolvability has been of interest to both theorists and experimentalists. Although canalization was originally proposed in the context of multicellular organisms, the effect of multicellularity and other classes of hierarchical organization on evolvability has not been considered by theoreticians. We address this issue using a Boolean population model with explicit representation of an environment in which individuals with explicit genotype and a hierarchical phenotype representing multicellularity evolve. Robustness is described by a single real number between zero and one which emerges from the genotype–phenotype map. We find that high robustness is favoured in constant environments, and lower robustness is favoured after environmental change. Multicellularity and hierarchical organization severely constrain robustness: peak evolvability occurs at an absolute level of robustness of about 0.99 compared with values of about 0.5 in a classical neutral network model. These constraints result in a sharp peak of evolvability in which the maximum is set by the fact that the fixation of adaptive mutations becomes more improbable as robustness decreases. When robustness is put under genetic control, robustness levels leading to maximum evolvability are selected for, but maximal relative fitness appears to require recombination. |
format | Online Article Text |
id | pubmed-10315174 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
spelling | pubmed-103151742023-07-02 The effect of mutational robustness on the evolvability of multicellular organisms and eukaryotic cells Jiang, Pengyao Kreitman, Martin Reinitz, John J Evol Biol Article Canalization involves mutational robustness, the lack of phenotypic change as a result of genetic mutations. Given the large divergence in phenotype across species, understanding the relationship between high robustness and evolvability has been of interest to both theorists and experimentalists. Although canalization was originally proposed in the context of multicellular organisms, the effect of multicellularity and other classes of hierarchical organization on evolvability has not been considered by theoreticians. We address this issue using a Boolean population model with explicit representation of an environment in which individuals with explicit genotype and a hierarchical phenotype representing multicellularity evolve. Robustness is described by a single real number between zero and one which emerges from the genotype–phenotype map. We find that high robustness is favoured in constant environments, and lower robustness is favoured after environmental change. Multicellularity and hierarchical organization severely constrain robustness: peak evolvability occurs at an absolute level of robustness of about 0.99 compared with values of about 0.5 in a classical neutral network model. These constraints result in a sharp peak of evolvability in which the maximum is set by the fact that the fixation of adaptive mutations becomes more improbable as robustness decreases. When robustness is put under genetic control, robustness levels leading to maximum evolvability are selected for, but maximal relative fitness appears to require recombination. 2023-06 2023-05-31 /pmc/articles/PMC10315174/ /pubmed/37256290 http://dx.doi.org/10.1111/jeb.14180 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the Creative Commons Attribution (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Jiang, Pengyao Kreitman, Martin Reinitz, John The effect of mutational robustness on the evolvability of multicellular organisms and eukaryotic cells |
title | The effect of mutational robustness on the evolvability of multicellular organisms and eukaryotic cells |
title_full | The effect of mutational robustness on the evolvability of multicellular organisms and eukaryotic cells |
title_fullStr | The effect of mutational robustness on the evolvability of multicellular organisms and eukaryotic cells |
title_full_unstemmed | The effect of mutational robustness on the evolvability of multicellular organisms and eukaryotic cells |
title_short | The effect of mutational robustness on the evolvability of multicellular organisms and eukaryotic cells |
title_sort | effect of mutational robustness on the evolvability of multicellular organisms and eukaryotic cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315174/ https://www.ncbi.nlm.nih.gov/pubmed/37256290 http://dx.doi.org/10.1111/jeb.14180 |
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