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The Coevolution of Cellularity and Metabolism Following the Origin of Life
The emergence of cellular organisms occurred sometime between the origin of life and the evolution of the last universal common ancestor and represents one of the major transitions in evolutionary history. Here we describe a series of artificial life simulations that reveal a close relationship betw...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer US
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7445158/ https://www.ncbi.nlm.nih.gov/pubmed/32809045 http://dx.doi.org/10.1007/s00239-020-09961-1 |
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author | Takagi, Yuta A. Nguyen, Diep H. Wexler, Tom B. Goldman, Aaron D. |
author_facet | Takagi, Yuta A. Nguyen, Diep H. Wexler, Tom B. Goldman, Aaron D. |
author_sort | Takagi, Yuta A. |
collection | PubMed |
description | The emergence of cellular organisms occurred sometime between the origin of life and the evolution of the last universal common ancestor and represents one of the major transitions in evolutionary history. Here we describe a series of artificial life simulations that reveal a close relationship between the evolution of cellularity, the evolution of metabolism, and the richness of the environment. When environments are rich in processing energy, a resource that the digital organisms require to both process their genomes and replicate, populations evolve toward a state of non-cellularity. But when processing energy is not readily available in the environment and organisms must produce their own processing energy from food puzzles, populations always evolve both a proficient metabolism and a high level of cellular impermeability. Even between these two environmental extremes, the population-averaged values of cellular impermeability and metabolic proficiency exhibit a very strong correlation with one another. Further investigations show that non-cellularity is selectively advantageous when environmental processing energy is abundant because it allows organisms to access the available energy, while cellularity is selectively advantageous when environmental processing energy is scarce because it affords organisms the genetic fidelity required to incrementally evolve efficient metabolisms. The selection pressures favoring either non-cellularity or cellularity can be reversed when the environment transitions from one of abundant processing energy to one of scarce processing energy. These results have important implications for when and why cellular organisms evolved following the origin of life. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00239-020-09961-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7445158 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-74451582020-08-31 The Coevolution of Cellularity and Metabolism Following the Origin of Life Takagi, Yuta A. Nguyen, Diep H. Wexler, Tom B. Goldman, Aaron D. J Mol Evol Original Article The emergence of cellular organisms occurred sometime between the origin of life and the evolution of the last universal common ancestor and represents one of the major transitions in evolutionary history. Here we describe a series of artificial life simulations that reveal a close relationship between the evolution of cellularity, the evolution of metabolism, and the richness of the environment. When environments are rich in processing energy, a resource that the digital organisms require to both process their genomes and replicate, populations evolve toward a state of non-cellularity. But when processing energy is not readily available in the environment and organisms must produce their own processing energy from food puzzles, populations always evolve both a proficient metabolism and a high level of cellular impermeability. Even between these two environmental extremes, the population-averaged values of cellular impermeability and metabolic proficiency exhibit a very strong correlation with one another. Further investigations show that non-cellularity is selectively advantageous when environmental processing energy is abundant because it allows organisms to access the available energy, while cellularity is selectively advantageous when environmental processing energy is scarce because it affords organisms the genetic fidelity required to incrementally evolve efficient metabolisms. The selection pressures favoring either non-cellularity or cellularity can be reversed when the environment transitions from one of abundant processing energy to one of scarce processing energy. These results have important implications for when and why cellular organisms evolved following the origin of life. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00239-020-09961-1) contains supplementary material, which is available to authorized users. Springer US 2020-08-18 2020 /pmc/articles/PMC7445158/ /pubmed/32809045 http://dx.doi.org/10.1007/s00239-020-09961-1 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Original Article Takagi, Yuta A. Nguyen, Diep H. Wexler, Tom B. Goldman, Aaron D. The Coevolution of Cellularity and Metabolism Following the Origin of Life |
title | The Coevolution of Cellularity and Metabolism Following the Origin of Life |
title_full | The Coevolution of Cellularity and Metabolism Following the Origin of Life |
title_fullStr | The Coevolution of Cellularity and Metabolism Following the Origin of Life |
title_full_unstemmed | The Coevolution of Cellularity and Metabolism Following the Origin of Life |
title_short | The Coevolution of Cellularity and Metabolism Following the Origin of Life |
title_sort | coevolution of cellularity and metabolism following the origin of life |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7445158/ https://www.ncbi.nlm.nih.gov/pubmed/32809045 http://dx.doi.org/10.1007/s00239-020-09961-1 |
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