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An incoherent feedforward loop facilitates adaptive tuning of gene expression

We studied adaptive evolution of gene expression using long-term experimental evolution of Saccharomyces cerevisiae in ammonium-limited chemostats. We found repeated selection for non-synonymous variation in the DNA binding domain of the transcriptional activator, GAT1, which functions with the repr...

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Autores principales: Hong, Jungeui, Brandt, Nathan, Abdul-Rahman, Farah, Yang, Ally, Hughes, Tim, Gresham, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903863/
https://www.ncbi.nlm.nih.gov/pubmed/29620523
http://dx.doi.org/10.7554/eLife.32323
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author Hong, Jungeui
Brandt, Nathan
Abdul-Rahman, Farah
Yang, Ally
Hughes, Tim
Gresham, David
author_facet Hong, Jungeui
Brandt, Nathan
Abdul-Rahman, Farah
Yang, Ally
Hughes, Tim
Gresham, David
author_sort Hong, Jungeui
collection PubMed
description We studied adaptive evolution of gene expression using long-term experimental evolution of Saccharomyces cerevisiae in ammonium-limited chemostats. We found repeated selection for non-synonymous variation in the DNA binding domain of the transcriptional activator, GAT1, which functions with the repressor, DAL80 in an incoherent type-1 feedforward loop (I1-FFL) to control expression of the high affinity ammonium transporter gene, MEP2. Missense mutations in the DNA binding domain of GAT1 reduce its binding to the GATAA consensus sequence. However, we show experimentally, and using mathematical modeling, that decreases in GAT1 binding result in increased expression of MEP2 as a consequence of properties of I1-FFLs. Our results show that I1-FFLs, one of the most commonly occurring network motifs in transcriptional networks, can facilitate adaptive tuning of gene expression through modulation of transcription factor binding affinities. Our findings highlight the importance of gene regulatory architectures in the evolution of gene expression.
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spelling pubmed-59038632018-04-18 An incoherent feedforward loop facilitates adaptive tuning of gene expression Hong, Jungeui Brandt, Nathan Abdul-Rahman, Farah Yang, Ally Hughes, Tim Gresham, David eLife Genetics and Genomics We studied adaptive evolution of gene expression using long-term experimental evolution of Saccharomyces cerevisiae in ammonium-limited chemostats. We found repeated selection for non-synonymous variation in the DNA binding domain of the transcriptional activator, GAT1, which functions with the repressor, DAL80 in an incoherent type-1 feedforward loop (I1-FFL) to control expression of the high affinity ammonium transporter gene, MEP2. Missense mutations in the DNA binding domain of GAT1 reduce its binding to the GATAA consensus sequence. However, we show experimentally, and using mathematical modeling, that decreases in GAT1 binding result in increased expression of MEP2 as a consequence of properties of I1-FFLs. Our results show that I1-FFLs, one of the most commonly occurring network motifs in transcriptional networks, can facilitate adaptive tuning of gene expression through modulation of transcription factor binding affinities. Our findings highlight the importance of gene regulatory architectures in the evolution of gene expression. eLife Sciences Publications, Ltd 2018-04-05 /pmc/articles/PMC5903863/ /pubmed/29620523 http://dx.doi.org/10.7554/eLife.32323 Text en © 2018, Hong 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 Genetics and Genomics
Hong, Jungeui
Brandt, Nathan
Abdul-Rahman, Farah
Yang, Ally
Hughes, Tim
Gresham, David
An incoherent feedforward loop facilitates adaptive tuning of gene expression
title An incoherent feedforward loop facilitates adaptive tuning of gene expression
title_full An incoherent feedforward loop facilitates adaptive tuning of gene expression
title_fullStr An incoherent feedforward loop facilitates adaptive tuning of gene expression
title_full_unstemmed An incoherent feedforward loop facilitates adaptive tuning of gene expression
title_short An incoherent feedforward loop facilitates adaptive tuning of gene expression
title_sort incoherent feedforward loop facilitates adaptive tuning of gene expression
topic Genetics and Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903863/
https://www.ncbi.nlm.nih.gov/pubmed/29620523
http://dx.doi.org/10.7554/eLife.32323
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