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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...

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Autores principales: Hsu, Chieh, Scherrer, Simone, Buetti-Dinh, Antoine, Ratna, Prasuna, Pizzolato, Julia, Jaquet, Vincent, Becskei, Attila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2012
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.
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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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