Parallel evolutionary dynamics of adaptive diversification in Escherichia coli.

The causes and mechanisms of evolutionary diversification are central issues in biology. Geographic isolation is the traditional explanation for diversification, but recent theoretical and empirical studies have shown that frequency-dependent selection can drive diversification without isolation and...

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Autores principales: Matthew D Herron, Michael Doebeli
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Publicado: Public Library of Science (PLoS) 2013
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spelling oai:doaj.org-article:e6f8e67991e44a3897fc134f77aeed592021-11-18T05:37:14ZParallel evolutionary dynamics of adaptive diversification in Escherichia coli.1544-91731545-788510.1371/journal.pbio.1001490https://doaj.org/article/e6f8e67991e44a3897fc134f77aeed592013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23431270/?tool=EBIhttps://doaj.org/toc/1544-9173https://doaj.org/toc/1545-7885The causes and mechanisms of evolutionary diversification are central issues in biology. Geographic isolation is the traditional explanation for diversification, but recent theoretical and empirical studies have shown that frequency-dependent selection can drive diversification without isolation and that adaptive diversification occurring in sympatry may be an important source of biological diversity. However, there are no empirical examples in which sympatric lineage splits have been understood at the genetic level, and it is unknown how predictable this process is-that is, whether similar ecological settings lead to parallel evolutionary dynamics of diversification. We documented the genetic basis and the evolutionary dynamics of adaptive diversification in three replicate evolution experiments, in which competition for two carbon sources caused initially isogenic populations of the bacterium Escherichia coli to diversify into two coexisting ecotypes representing different physiological adaptations in the central carbohydrate metabolism. Whole-genome sequencing of clones of each ecotype from different populations revealed many parallel and some unique genetic changes underlying the derived phenotypes, including changes to the same genes and sometimes to the same nucleotide. Timelines of allele frequencies extracted from the frozen "fossil" record of the three evolving populations suggest parallel evolutionary dynamics driven at least in part by a co-evolutionary process in which mutations causing one type of physiology changed the ecological environment, allowing the invasion of mutations causing an alternate physiology. This process closely corresponds to the evolutionary dynamics seen in mathematical models of adaptive diversification due to frequency-dependent ecological interactions. The parallel genetic changes underlying similar phenotypes in independently evolved lineages provide empirical evidence of adaptive diversification as a predictable evolutionary process.Matthew D HerronMichael DoebeliPublic Library of Science (PLoS)articleBiology (General)QH301-705.5ENPLoS Biology, Vol 11, Iss 2, p e1001490 (2013)
institution DOAJ
collection DOAJ
language EN
topic Biology (General)
QH301-705.5
spellingShingle Biology (General)
QH301-705.5
Matthew D Herron
Michael Doebeli
Parallel evolutionary dynamics of adaptive diversification in Escherichia coli.
description The causes and mechanisms of evolutionary diversification are central issues in biology. Geographic isolation is the traditional explanation for diversification, but recent theoretical and empirical studies have shown that frequency-dependent selection can drive diversification without isolation and that adaptive diversification occurring in sympatry may be an important source of biological diversity. However, there are no empirical examples in which sympatric lineage splits have been understood at the genetic level, and it is unknown how predictable this process is-that is, whether similar ecological settings lead to parallel evolutionary dynamics of diversification. We documented the genetic basis and the evolutionary dynamics of adaptive diversification in three replicate evolution experiments, in which competition for two carbon sources caused initially isogenic populations of the bacterium Escherichia coli to diversify into two coexisting ecotypes representing different physiological adaptations in the central carbohydrate metabolism. Whole-genome sequencing of clones of each ecotype from different populations revealed many parallel and some unique genetic changes underlying the derived phenotypes, including changes to the same genes and sometimes to the same nucleotide. Timelines of allele frequencies extracted from the frozen "fossil" record of the three evolving populations suggest parallel evolutionary dynamics driven at least in part by a co-evolutionary process in which mutations causing one type of physiology changed the ecological environment, allowing the invasion of mutations causing an alternate physiology. This process closely corresponds to the evolutionary dynamics seen in mathematical models of adaptive diversification due to frequency-dependent ecological interactions. The parallel genetic changes underlying similar phenotypes in independently evolved lineages provide empirical evidence of adaptive diversification as a predictable evolutionary process.
format article
author Matthew D Herron
Michael Doebeli
author_facet Matthew D Herron
Michael Doebeli
author_sort Matthew D Herron
title Parallel evolutionary dynamics of adaptive diversification in Escherichia coli.
title_short Parallel evolutionary dynamics of adaptive diversification in Escherichia coli.
title_full Parallel evolutionary dynamics of adaptive diversification in Escherichia coli.
title_fullStr Parallel evolutionary dynamics of adaptive diversification in Escherichia coli.
title_full_unstemmed Parallel evolutionary dynamics of adaptive diversification in Escherichia coli.
title_sort parallel evolutionary dynamics of adaptive diversification in escherichia coli.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/e6f8e67991e44a3897fc134f77aeed59
work_keys_str_mv AT matthewdherron parallelevolutionarydynamicsofadaptivediversificationinescherichiacoli
AT michaeldoebeli parallelevolutionarydynamicsofadaptivediversificationinescherichiacoli
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