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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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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. |
format | Online Article Text |
id | pubmed-6546794 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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