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Feed-forward regulation adaptively evolves via dynamics rather than topology when there is intrinsic noise

In transcriptional regulatory networks (TRNs), a canonical 3-node feed-forward loop (FFL) is hypothesized to evolve to filter out short spurious signals. We test this adaptive hypothesis against a novel null evolutionary model. Our mutational model captures the intrinsically high prevalence of weak...

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Autores principales: Xiong, Kun, Lancaster, Alex K., Siegal, Mark L., Masel, Joanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6546794/
https://www.ncbi.nlm.nih.gov/pubmed/31160574
http://dx.doi.org/10.1038/s41467-019-10388-6
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author Xiong, Kun
Lancaster, Alex K.
Siegal, Mark L.
Masel, Joanna
author_facet Xiong, Kun
Lancaster, Alex K.
Siegal, Mark L.
Masel, Joanna
author_sort Xiong, Kun
collection PubMed
description In transcriptional regulatory networks (TRNs), a canonical 3-node feed-forward loop (FFL) is hypothesized to evolve to filter out short spurious signals. We test this adaptive hypothesis against a novel null evolutionary model. Our mutational model captures the intrinsically high prevalence of weak affinity transcription factor binding sites. We also capture stochasticity and delays in gene expression that distort external signals and intrinsically generate noise. Functional FFLs evolve readily under selection for the hypothesized function but not in negative controls. Interestingly, a 4-node “diamond” motif also emerges as a short spurious signal filter. The diamond uses expression dynamics rather than path length to provide fast and slow pathways. When there is no idealized external spurious signal to filter out, but only internally generated noise, only the diamond and not the FFL evolves. While our results support the adaptive hypothesis, we also show that non-adaptive factors, including the intrinsic expression dynamics, matter.
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spelling pubmed-65467942019-06-18 Feed-forward regulation adaptively evolves via dynamics rather than topology when there is intrinsic noise Xiong, Kun Lancaster, Alex K. Siegal, Mark L. Masel, Joanna Nat Commun Article In transcriptional regulatory networks (TRNs), a canonical 3-node feed-forward loop (FFL) is hypothesized to evolve to filter out short spurious signals. We test this adaptive hypothesis against a novel null evolutionary model. Our mutational model captures the intrinsically high prevalence of weak affinity transcription factor binding sites. We also capture stochasticity and delays in gene expression that distort external signals and intrinsically generate noise. Functional FFLs evolve readily under selection for the hypothesized function but not in negative controls. Interestingly, a 4-node “diamond” motif also emerges as a short spurious signal filter. The diamond uses expression dynamics rather than path length to provide fast and slow pathways. When there is no idealized external spurious signal to filter out, but only internally generated noise, only the diamond and not the FFL evolves. While our results support the adaptive hypothesis, we also show that non-adaptive factors, including the intrinsic expression dynamics, matter. Nature Publishing Group UK 2019-06-03 /pmc/articles/PMC6546794/ /pubmed/31160574 http://dx.doi.org/10.1038/s41467-019-10388-6 Text en © The Author(s) 2019 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
Xiong, Kun
Lancaster, Alex K.
Siegal, Mark L.
Masel, Joanna
Feed-forward regulation adaptively evolves via dynamics rather than topology when there is intrinsic noise
title Feed-forward regulation adaptively evolves via dynamics rather than topology when there is intrinsic noise
title_full Feed-forward regulation adaptively evolves via dynamics rather than topology when there is intrinsic noise
title_fullStr Feed-forward regulation adaptively evolves via dynamics rather than topology when there is intrinsic noise
title_full_unstemmed Feed-forward regulation adaptively evolves via dynamics rather than topology when there is intrinsic noise
title_short Feed-forward regulation adaptively evolves via dynamics rather than topology when there is intrinsic noise
title_sort feed-forward regulation adaptively evolves via dynamics rather than topology when there is intrinsic noise
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6546794/
https://www.ncbi.nlm.nih.gov/pubmed/31160574
http://dx.doi.org/10.1038/s41467-019-10388-6
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