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Ongoing resolution of duplicate gene functions shapes the diversification of a metabolic network

The evolutionary mechanisms leading to duplicate gene retention are well understood, but the long-term impacts of paralog differentiation on the regulation of metabolism remain underappreciated. Here we experimentally dissect the functions of two pairs of ancient paralogs of the GALactose sugar util...

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Autores principales: Kuang, Meihua Christina, Hutchins, Paul D, Russell, Jason D, Coon, Joshua J, Hittinger, Chris Todd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5089864/
https://www.ncbi.nlm.nih.gov/pubmed/27690225
http://dx.doi.org/10.7554/eLife.19027
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author Kuang, Meihua Christina
Hutchins, Paul D
Russell, Jason D
Coon, Joshua J
Hittinger, Chris Todd
author_facet Kuang, Meihua Christina
Hutchins, Paul D
Russell, Jason D
Coon, Joshua J
Hittinger, Chris Todd
author_sort Kuang, Meihua Christina
collection PubMed
description The evolutionary mechanisms leading to duplicate gene retention are well understood, but the long-term impacts of paralog differentiation on the regulation of metabolism remain underappreciated. Here we experimentally dissect the functions of two pairs of ancient paralogs of the GALactose sugar utilization network in two yeast species. We show that the Saccharomyces uvarum network is more active, even as over-induction is prevented by a second co-repressor that the model yeast Saccharomyces cerevisiae lacks. Surprisingly, removal of this repression system leads to a strong growth arrest, likely due to overly rapid galactose catabolism and metabolic overload. Alternative sugars, such as fructose, circumvent metabolic control systems and exacerbate this phenotype. We further show that S. cerevisiae experiences homologous metabolic constraints that are subtler due to how the paralogs have diversified. These results show how the functional differentiation of paralogs continues to shape regulatory network architectures and metabolic strategies long after initial preservation. DOI: http://dx.doi.org/10.7554/eLife.19027.001
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spelling pubmed-50898642016-11-03 Ongoing resolution of duplicate gene functions shapes the diversification of a metabolic network Kuang, Meihua Christina Hutchins, Paul D Russell, Jason D Coon, Joshua J Hittinger, Chris Todd eLife Genomics and Evolutionary Biology The evolutionary mechanisms leading to duplicate gene retention are well understood, but the long-term impacts of paralog differentiation on the regulation of metabolism remain underappreciated. Here we experimentally dissect the functions of two pairs of ancient paralogs of the GALactose sugar utilization network in two yeast species. We show that the Saccharomyces uvarum network is more active, even as over-induction is prevented by a second co-repressor that the model yeast Saccharomyces cerevisiae lacks. Surprisingly, removal of this repression system leads to a strong growth arrest, likely due to overly rapid galactose catabolism and metabolic overload. Alternative sugars, such as fructose, circumvent metabolic control systems and exacerbate this phenotype. We further show that S. cerevisiae experiences homologous metabolic constraints that are subtler due to how the paralogs have diversified. These results show how the functional differentiation of paralogs continues to shape regulatory network architectures and metabolic strategies long after initial preservation. DOI: http://dx.doi.org/10.7554/eLife.19027.001 eLife Sciences Publications, Ltd 2016-09-30 /pmc/articles/PMC5089864/ /pubmed/27690225 http://dx.doi.org/10.7554/eLife.19027 Text en © 2016, Kuang et al 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 Genomics and Evolutionary Biology
Kuang, Meihua Christina
Hutchins, Paul D
Russell, Jason D
Coon, Joshua J
Hittinger, Chris Todd
Ongoing resolution of duplicate gene functions shapes the diversification of a metabolic network
title Ongoing resolution of duplicate gene functions shapes the diversification of a metabolic network
title_full Ongoing resolution of duplicate gene functions shapes the diversification of a metabolic network
title_fullStr Ongoing resolution of duplicate gene functions shapes the diversification of a metabolic network
title_full_unstemmed Ongoing resolution of duplicate gene functions shapes the diversification of a metabolic network
title_short Ongoing resolution of duplicate gene functions shapes the diversification of a metabolic network
title_sort ongoing resolution of duplicate gene functions shapes the diversification of a metabolic network
topic Genomics and Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5089864/
https://www.ncbi.nlm.nih.gov/pubmed/27690225
http://dx.doi.org/10.7554/eLife.19027
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