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Mutations that improve efficiency of a weak-link enzyme are rare compared to adaptive mutations elsewhere in the genome
New enzymes often evolve by gene amplification and divergence. Previous experimental studies have followed the evolutionary trajectory of an amplified gene, but have not considered mutations elsewhere in the genome when fitness is limited by an evolving gene. We have evolved a strain of Escherichia...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6941894/ https://www.ncbi.nlm.nih.gov/pubmed/31815667 http://dx.doi.org/10.7554/eLife.53535 |
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author | Morgenthaler, Andrew B Kinney, Wallis R Ebmeier, Christopher C Walsh, Corinne M Snyder, Daniel J Cooper, Vaughn S Old, William M Copley, Shelley D |
author_facet | Morgenthaler, Andrew B Kinney, Wallis R Ebmeier, Christopher C Walsh, Corinne M Snyder, Daniel J Cooper, Vaughn S Old, William M Copley, Shelley D |
author_sort | Morgenthaler, Andrew B |
collection | PubMed |
description | New enzymes often evolve by gene amplification and divergence. Previous experimental studies have followed the evolutionary trajectory of an amplified gene, but have not considered mutations elsewhere in the genome when fitness is limited by an evolving gene. We have evolved a strain of Escherichia coli in which a secondary promiscuous activity has been recruited to serve an essential function. The gene encoding the ‘weak-link’ enzyme amplified in all eight populations, but mutations improving the newly needed activity occurred in only one. Most adaptive mutations occurred elsewhere in the genome. Some mutations increase expression of the enzyme upstream of the weak-link enzyme, pushing material through the dysfunctional metabolic pathway. Others enhance production of a co-substrate for a downstream enzyme, thereby pulling material through the pathway. Most of these latter mutations are detrimental in wild-type E. coli, and thus would require reversion or compensation once a sufficient new activity has evolved. |
format | Online Article Text |
id | pubmed-6941894 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-69418942020-01-06 Mutations that improve efficiency of a weak-link enzyme are rare compared to adaptive mutations elsewhere in the genome Morgenthaler, Andrew B Kinney, Wallis R Ebmeier, Christopher C Walsh, Corinne M Snyder, Daniel J Cooper, Vaughn S Old, William M Copley, Shelley D eLife Evolutionary Biology New enzymes often evolve by gene amplification and divergence. Previous experimental studies have followed the evolutionary trajectory of an amplified gene, but have not considered mutations elsewhere in the genome when fitness is limited by an evolving gene. We have evolved a strain of Escherichia coli in which a secondary promiscuous activity has been recruited to serve an essential function. The gene encoding the ‘weak-link’ enzyme amplified in all eight populations, but mutations improving the newly needed activity occurred in only one. Most adaptive mutations occurred elsewhere in the genome. Some mutations increase expression of the enzyme upstream of the weak-link enzyme, pushing material through the dysfunctional metabolic pathway. Others enhance production of a co-substrate for a downstream enzyme, thereby pulling material through the pathway. Most of these latter mutations are detrimental in wild-type E. coli, and thus would require reversion or compensation once a sufficient new activity has evolved. eLife Sciences Publications, Ltd 2019-12-09 /pmc/articles/PMC6941894/ /pubmed/31815667 http://dx.doi.org/10.7554/eLife.53535 Text en © 2019, Morgenthaler et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Evolutionary Biology Morgenthaler, Andrew B Kinney, Wallis R Ebmeier, Christopher C Walsh, Corinne M Snyder, Daniel J Cooper, Vaughn S Old, William M Copley, Shelley D Mutations that improve efficiency of a weak-link enzyme are rare compared to adaptive mutations elsewhere in the genome |
title | Mutations that improve efficiency of a weak-link enzyme are rare compared to adaptive mutations elsewhere in the genome |
title_full | Mutations that improve efficiency of a weak-link enzyme are rare compared to adaptive mutations elsewhere in the genome |
title_fullStr | Mutations that improve efficiency of a weak-link enzyme are rare compared to adaptive mutations elsewhere in the genome |
title_full_unstemmed | Mutations that improve efficiency of a weak-link enzyme are rare compared to adaptive mutations elsewhere in the genome |
title_short | Mutations that improve efficiency of a weak-link enzyme are rare compared to adaptive mutations elsewhere in the genome |
title_sort | mutations that improve efficiency of a weak-link enzyme are rare compared to adaptive mutations elsewhere in the genome |
topic | Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6941894/ https://www.ncbi.nlm.nih.gov/pubmed/31815667 http://dx.doi.org/10.7554/eLife.53535 |
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