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Complex small-world regulatory networks emerge from the 3D organisation of the human genome

The discovery that overexpressing one or a few critical transcription factors can switch cell state suggests that gene regulatory networks are relatively simple. In contrast, genome-wide association studies (GWAS) point to complex phenotypes being determined by hundreds of loci that rarely encode tr...

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Autores principales: Brackley, C. A., Gilbert, N., Michieletto, D., Papantonis, A., Pereira, M. C. F., Cook, P. R., Marenduzzo, D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8486811/
https://www.ncbi.nlm.nih.gov/pubmed/34599163
http://dx.doi.org/10.1038/s41467-021-25875-y
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author Brackley, C. A.
Gilbert, N.
Michieletto, D.
Papantonis, A.
Pereira, M. C. F.
Cook, P. R.
Marenduzzo, D.
author_facet Brackley, C. A.
Gilbert, N.
Michieletto, D.
Papantonis, A.
Pereira, M. C. F.
Cook, P. R.
Marenduzzo, D.
author_sort Brackley, C. A.
collection PubMed
description The discovery that overexpressing one or a few critical transcription factors can switch cell state suggests that gene regulatory networks are relatively simple. In contrast, genome-wide association studies (GWAS) point to complex phenotypes being determined by hundreds of loci that rarely encode transcription factors and which individually have small effects. Here, we use computer simulations and a simple fitting-free polymer model of chromosomes to show that spatial correlations arising from 3D genome organisation naturally lead to stochastic and bursty transcription as well as complex small-world regulatory networks (where the transcriptional activity of each genomic region subtly affects almost all others). These effects require factors to be present at sub-saturating levels; increasing levels dramatically simplifies networks as more transcription units are pressed into use. Consequently, results from GWAS can be reconciled with those involving overexpression. We apply this pan-genomic model to predict patterns of transcriptional activity in whole human chromosomes, and, as an example, the effects of the deletion causing the diGeorge syndrome.
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spelling pubmed-84868112021-10-07 Complex small-world regulatory networks emerge from the 3D organisation of the human genome Brackley, C. A. Gilbert, N. Michieletto, D. Papantonis, A. Pereira, M. C. F. Cook, P. R. Marenduzzo, D. Nat Commun Article The discovery that overexpressing one or a few critical transcription factors can switch cell state suggests that gene regulatory networks are relatively simple. In contrast, genome-wide association studies (GWAS) point to complex phenotypes being determined by hundreds of loci that rarely encode transcription factors and which individually have small effects. Here, we use computer simulations and a simple fitting-free polymer model of chromosomes to show that spatial correlations arising from 3D genome organisation naturally lead to stochastic and bursty transcription as well as complex small-world regulatory networks (where the transcriptional activity of each genomic region subtly affects almost all others). These effects require factors to be present at sub-saturating levels; increasing levels dramatically simplifies networks as more transcription units are pressed into use. Consequently, results from GWAS can be reconciled with those involving overexpression. We apply this pan-genomic model to predict patterns of transcriptional activity in whole human chromosomes, and, as an example, the effects of the deletion causing the diGeorge syndrome. Nature Publishing Group UK 2021-10-01 /pmc/articles/PMC8486811/ /pubmed/34599163 http://dx.doi.org/10.1038/s41467-021-25875-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Brackley, C. A.
Gilbert, N.
Michieletto, D.
Papantonis, A.
Pereira, M. C. F.
Cook, P. R.
Marenduzzo, D.
Complex small-world regulatory networks emerge from the 3D organisation of the human genome
title Complex small-world regulatory networks emerge from the 3D organisation of the human genome
title_full Complex small-world regulatory networks emerge from the 3D organisation of the human genome
title_fullStr Complex small-world regulatory networks emerge from the 3D organisation of the human genome
title_full_unstemmed Complex small-world regulatory networks emerge from the 3D organisation of the human genome
title_short Complex small-world regulatory networks emerge from the 3D organisation of the human genome
title_sort complex small-world regulatory networks emerge from the 3d organisation of the human genome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8486811/
https://www.ncbi.nlm.nih.gov/pubmed/34599163
http://dx.doi.org/10.1038/s41467-021-25875-y
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