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Evolution of new regulatory functions on biophysically realistic fitness landscapes

Gene expression is controlled by networks of regulatory proteins that interact specifically with external signals and DNA regulatory sequences. These interactions force the network components to co-evolve so as to continually maintain function. Yet, existing models of evolution mostly focus on isola...

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Detalles Bibliográficos
Autores principales: Friedlander, Tamar, Prizak, Roshan, Barton, Nicholas H., Tkačik, Gašper
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548793/
https://www.ncbi.nlm.nih.gov/pubmed/28790313
http://dx.doi.org/10.1038/s41467-017-00238-8
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author Friedlander, Tamar
Prizak, Roshan
Barton, Nicholas H.
Tkačik, Gašper
author_facet Friedlander, Tamar
Prizak, Roshan
Barton, Nicholas H.
Tkačik, Gašper
author_sort Friedlander, Tamar
collection PubMed
description Gene expression is controlled by networks of regulatory proteins that interact specifically with external signals and DNA regulatory sequences. These interactions force the network components to co-evolve so as to continually maintain function. Yet, existing models of evolution mostly focus on isolated genetic elements. In contrast, we study the essential process by which regulatory networks grow: the duplication and subsequent specialization of network components. We synthesize a biophysical model of molecular interactions with the evolutionary framework to find the conditions and pathways by which new regulatory functions emerge. We show that specialization of new network components is usually slow, but can be drastically accelerated in the presence of regulatory crosstalk and mutations that promote promiscuous interactions between network components.
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spelling pubmed-55487932017-08-11 Evolution of new regulatory functions on biophysically realistic fitness landscapes Friedlander, Tamar Prizak, Roshan Barton, Nicholas H. Tkačik, Gašper Nat Commun Article Gene expression is controlled by networks of regulatory proteins that interact specifically with external signals and DNA regulatory sequences. These interactions force the network components to co-evolve so as to continually maintain function. Yet, existing models of evolution mostly focus on isolated genetic elements. In contrast, we study the essential process by which regulatory networks grow: the duplication and subsequent specialization of network components. We synthesize a biophysical model of molecular interactions with the evolutionary framework to find the conditions and pathways by which new regulatory functions emerge. We show that specialization of new network components is usually slow, but can be drastically accelerated in the presence of regulatory crosstalk and mutations that promote promiscuous interactions between network components. Nature Publishing Group UK 2017-08-09 /pmc/articles/PMC5548793/ /pubmed/28790313 http://dx.doi.org/10.1038/s41467-017-00238-8 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Friedlander, Tamar
Prizak, Roshan
Barton, Nicholas H.
Tkačik, Gašper
Evolution of new regulatory functions on biophysically realistic fitness landscapes
title Evolution of new regulatory functions on biophysically realistic fitness landscapes
title_full Evolution of new regulatory functions on biophysically realistic fitness landscapes
title_fullStr Evolution of new regulatory functions on biophysically realistic fitness landscapes
title_full_unstemmed Evolution of new regulatory functions on biophysically realistic fitness landscapes
title_short Evolution of new regulatory functions on biophysically realistic fitness landscapes
title_sort evolution of new regulatory functions on biophysically realistic fitness landscapes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548793/
https://www.ncbi.nlm.nih.gov/pubmed/28790313
http://dx.doi.org/10.1038/s41467-017-00238-8
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