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Darwinian evolution as a dynamical principle

Darwinian evolution (DE)—biology’s powerful process of adaptation—is remarkably different from other known dynamical processes. It is antithermodynamic, driving away from equilibrium; it has persisted for 3.5 billion years; and its target, fitness, can seem like “Just So” stories. For insights, we m...

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Detalles Bibliográficos
Autores principales: Kocher, Charles D., Dill, Ken A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10089213/
https://www.ncbi.nlm.nih.gov/pubmed/36881627
http://dx.doi.org/10.1073/pnas.2218390120
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author Kocher, Charles D.
Dill, Ken A.
author_facet Kocher, Charles D.
Dill, Ken A.
author_sort Kocher, Charles D.
collection PubMed
description Darwinian evolution (DE)—biology’s powerful process of adaptation—is remarkably different from other known dynamical processes. It is antithermodynamic, driving away from equilibrium; it has persisted for 3.5 billion years; and its target, fitness, can seem like “Just So” stories. For insights, we make a computational model. In the Darwinian Evolution Machine (DEM) model, resource-driven duplication and competition operate inside a cycle of search/compete/choose. We find the following: 1) DE requires multiorganism coexistence for its long-term persistence and ability to cross fitness valleys. 2) DE is driven by resource dynamics, like booms and busts, not just by mutational change. And, 3) fitness ratcheting requires a mechanistic separation between variation and selection steps, perhaps explaining biology’s use of separate polymers, DNA and proteins.
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spelling pubmed-100892132023-09-07 Darwinian evolution as a dynamical principle Kocher, Charles D. Dill, Ken A. Proc Natl Acad Sci U S A Physical Sciences Darwinian evolution (DE)—biology’s powerful process of adaptation—is remarkably different from other known dynamical processes. It is antithermodynamic, driving away from equilibrium; it has persisted for 3.5 billion years; and its target, fitness, can seem like “Just So” stories. For insights, we make a computational model. In the Darwinian Evolution Machine (DEM) model, resource-driven duplication and competition operate inside a cycle of search/compete/choose. We find the following: 1) DE requires multiorganism coexistence for its long-term persistence and ability to cross fitness valleys. 2) DE is driven by resource dynamics, like booms and busts, not just by mutational change. And, 3) fitness ratcheting requires a mechanistic separation between variation and selection steps, perhaps explaining biology’s use of separate polymers, DNA and proteins. National Academy of Sciences 2023-03-07 2023-03-14 /pmc/articles/PMC10089213/ /pubmed/36881627 http://dx.doi.org/10.1073/pnas.2218390120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Physical Sciences
Kocher, Charles D.
Dill, Ken A.
Darwinian evolution as a dynamical principle
title Darwinian evolution as a dynamical principle
title_full Darwinian evolution as a dynamical principle
title_fullStr Darwinian evolution as a dynamical principle
title_full_unstemmed Darwinian evolution as a dynamical principle
title_short Darwinian evolution as a dynamical principle
title_sort darwinian evolution as a dynamical principle
topic Physical Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10089213/
https://www.ncbi.nlm.nih.gov/pubmed/36881627
http://dx.doi.org/10.1073/pnas.2218390120
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