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Stochastic signalling rewires the interaction map of a multiple feedback network during yeast evolution
During evolution, genetic networks are rewired through strengthening or weakening their interactions to develop new regulatory schemes. In the galactose network, the GAL1/GAL3 paralogues and the GAL2 gene enhance their own expression mediated by the Gal4p transcriptional activator. The wiring streng...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3293423/ https://www.ncbi.nlm.nih.gov/pubmed/22353713 http://dx.doi.org/10.1038/ncomms1687 |
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author | Hsu, Chieh Scherrer, Simone Buetti-Dinh, Antoine Ratna, Prasuna Pizzolato, Julia Jaquet, Vincent Becskei, Attila |
author_facet | Hsu, Chieh Scherrer, Simone Buetti-Dinh, Antoine Ratna, Prasuna Pizzolato, Julia Jaquet, Vincent Becskei, Attila |
author_sort | Hsu, Chieh |
collection | PubMed |
description | During evolution, genetic networks are rewired through strengthening or weakening their interactions to develop new regulatory schemes. In the galactose network, the GAL1/GAL3 paralogues and the GAL2 gene enhance their own expression mediated by the Gal4p transcriptional activator. The wiring strength in these feedback loops is set by the number of Gal4p binding sites. Here we show using synthetic circuits that multiplying the binding sites increases the expression of a gene under the direct control of an activator, but this enhancement is not fed back in the circuit. The feedback loops are rather activated by genes that have frequent stochastic bursts and fast RNA decay rates. In this way, rapid adaptation to galactose can be triggered even by weakly expressed genes. Our results indicate that nonlinear stochastic transcriptional responses enable feedback loops to function autonomously, or contrary to what is dictated by the strength of interactions enclosing the circuit. |
format | Online Article Text |
id | pubmed-3293423 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-32934232012-03-05 Stochastic signalling rewires the interaction map of a multiple feedback network during yeast evolution Hsu, Chieh Scherrer, Simone Buetti-Dinh, Antoine Ratna, Prasuna Pizzolato, Julia Jaquet, Vincent Becskei, Attila Nat Commun Article During evolution, genetic networks are rewired through strengthening or weakening their interactions to develop new regulatory schemes. In the galactose network, the GAL1/GAL3 paralogues and the GAL2 gene enhance their own expression mediated by the Gal4p transcriptional activator. The wiring strength in these feedback loops is set by the number of Gal4p binding sites. Here we show using synthetic circuits that multiplying the binding sites increases the expression of a gene under the direct control of an activator, but this enhancement is not fed back in the circuit. The feedback loops are rather activated by genes that have frequent stochastic bursts and fast RNA decay rates. In this way, rapid adaptation to galactose can be triggered even by weakly expressed genes. Our results indicate that nonlinear stochastic transcriptional responses enable feedback loops to function autonomously, or contrary to what is dictated by the strength of interactions enclosing the circuit. Nature Pub. Group 2012-02-21 /pmc/articles/PMC3293423/ /pubmed/22353713 http://dx.doi.org/10.1038/ncomms1687 Text en Copyright © 2012, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Article Hsu, Chieh Scherrer, Simone Buetti-Dinh, Antoine Ratna, Prasuna Pizzolato, Julia Jaquet, Vincent Becskei, Attila Stochastic signalling rewires the interaction map of a multiple feedback network during yeast evolution |
title | Stochastic signalling rewires the interaction map of a multiple feedback network during yeast evolution |
title_full | Stochastic signalling rewires the interaction map of a multiple feedback network during yeast evolution |
title_fullStr | Stochastic signalling rewires the interaction map of a multiple feedback network during yeast evolution |
title_full_unstemmed | Stochastic signalling rewires the interaction map of a multiple feedback network during yeast evolution |
title_short | Stochastic signalling rewires the interaction map of a multiple feedback network during yeast evolution |
title_sort | stochastic signalling rewires the interaction map of a multiple feedback network during yeast evolution |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3293423/ https://www.ncbi.nlm.nih.gov/pubmed/22353713 http://dx.doi.org/10.1038/ncomms1687 |
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