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Assigning function to natural allelic variation via dynamic modeling of gene network induction
More and more natural DNA variants are being linked to physiological traits. Yet, understanding what differences they make on molecular regulations remains challenging. Important properties of gene regulatory networks can be captured by computational models. If model parameters can be “personalized”...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5787706/ https://www.ncbi.nlm.nih.gov/pubmed/29335276 http://dx.doi.org/10.15252/msb.20177803 |
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author | Richard, Magali Chuffart, Florent Duplus‐Bottin, Hélène Pouyet, Fanny Spichty, Martin Fulcrand, Etienne Entrevan, Marianne Barthelaix, Audrey Springer, Michael Jost, Daniel Yvert, Gaël |
author_facet | Richard, Magali Chuffart, Florent Duplus‐Bottin, Hélène Pouyet, Fanny Spichty, Martin Fulcrand, Etienne Entrevan, Marianne Barthelaix, Audrey Springer, Michael Jost, Daniel Yvert, Gaël |
author_sort | Richard, Magali |
collection | PubMed |
description | More and more natural DNA variants are being linked to physiological traits. Yet, understanding what differences they make on molecular regulations remains challenging. Important properties of gene regulatory networks can be captured by computational models. If model parameters can be “personalized” according to the genotype, their variation may then reveal how DNA variants operate in the network. Here, we combined experiments and computations to visualize natural alleles of the yeast GAL3 gene in a space of model parameters describing the galactose response network. Alleles altering the activation of Gal3p by galactose were discriminated from those affecting its activity (production/degradation or efficiency of the activated protein). The approach allowed us to correctly predict that a non‐synonymous SNP would change the binding affinity of Gal3p with the Gal80p transcriptional repressor. Our results illustrate how personalizing gene regulatory models can be used for the mechanistic interpretation of genetic variants. |
format | Online Article Text |
id | pubmed-5787706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57877062018-02-08 Assigning function to natural allelic variation via dynamic modeling of gene network induction Richard, Magali Chuffart, Florent Duplus‐Bottin, Hélène Pouyet, Fanny Spichty, Martin Fulcrand, Etienne Entrevan, Marianne Barthelaix, Audrey Springer, Michael Jost, Daniel Yvert, Gaël Mol Syst Biol Articles More and more natural DNA variants are being linked to physiological traits. Yet, understanding what differences they make on molecular regulations remains challenging. Important properties of gene regulatory networks can be captured by computational models. If model parameters can be “personalized” according to the genotype, their variation may then reveal how DNA variants operate in the network. Here, we combined experiments and computations to visualize natural alleles of the yeast GAL3 gene in a space of model parameters describing the galactose response network. Alleles altering the activation of Gal3p by galactose were discriminated from those affecting its activity (production/degradation or efficiency of the activated protein). The approach allowed us to correctly predict that a non‐synonymous SNP would change the binding affinity of Gal3p with the Gal80p transcriptional repressor. Our results illustrate how personalizing gene regulatory models can be used for the mechanistic interpretation of genetic variants. John Wiley and Sons Inc. 2018-01-15 /pmc/articles/PMC5787706/ /pubmed/29335276 http://dx.doi.org/10.15252/msb.20177803 Text en © 2018 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the Creative Commons Attribution 4.0 (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Richard, Magali Chuffart, Florent Duplus‐Bottin, Hélène Pouyet, Fanny Spichty, Martin Fulcrand, Etienne Entrevan, Marianne Barthelaix, Audrey Springer, Michael Jost, Daniel Yvert, Gaël Assigning function to natural allelic variation via dynamic modeling of gene network induction |
title | Assigning function to natural allelic variation via dynamic modeling of gene network induction |
title_full | Assigning function to natural allelic variation via dynamic modeling of gene network induction |
title_fullStr | Assigning function to natural allelic variation via dynamic modeling of gene network induction |
title_full_unstemmed | Assigning function to natural allelic variation via dynamic modeling of gene network induction |
title_short | Assigning function to natural allelic variation via dynamic modeling of gene network induction |
title_sort | assigning function to natural allelic variation via dynamic modeling of gene network induction |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5787706/ https://www.ncbi.nlm.nih.gov/pubmed/29335276 http://dx.doi.org/10.15252/msb.20177803 |
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