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WASABI: a dynamic iterative framework for gene regulatory network inference
BACKGROUND: Inference of gene regulatory networks from gene expression data has been a long-standing and notoriously difficult task in systems biology. Recently, single-cell transcriptomic data have been massively used for gene regulatory network inference, with both successes and limitations. RESUL...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6498543/ https://www.ncbi.nlm.nih.gov/pubmed/31046682 http://dx.doi.org/10.1186/s12859-019-2798-1 |
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author | Bonnaffoux, Arnaud Herbach, Ulysse Richard, Angélique Guillemin, Anissa Gonin-Giraud, Sandrine Gros, Pierre-Alexis Gandrillon, Olivier |
author_facet | Bonnaffoux, Arnaud Herbach, Ulysse Richard, Angélique Guillemin, Anissa Gonin-Giraud, Sandrine Gros, Pierre-Alexis Gandrillon, Olivier |
author_sort | Bonnaffoux, Arnaud |
collection | PubMed |
description | BACKGROUND: Inference of gene regulatory networks from gene expression data has been a long-standing and notoriously difficult task in systems biology. Recently, single-cell transcriptomic data have been massively used for gene regulatory network inference, with both successes and limitations. RESULTS: In the present work we propose an iterative algorithm called WASABI, dedicated to inferring a causal dynamical network from time-stamped single-cell data, which tackles some of the limitations associated with current approaches. We first introduce the concept of waves, which posits that the information provided by an external stimulus will affect genes one-by-one through a cascade, like waves spreading through a network. This concept allows us to infer the network one gene at a time, after genes have been ordered regarding their time of regulation. We then demonstrate the ability of WASABI to correctly infer small networks, which have been simulated in silico using a mechanistic model consisting of coupled piecewise-deterministic Markov processes for the proper description of gene expression at the single-cell level. We finally apply WASABI on in vitro generated data on an avian model of erythroid differentiation. The structure of the resulting gene regulatory network sheds a new light on the molecular mechanisms controlling this process. In particular, we find no evidence for hub genes and a much more distributed network structure than expected. Interestingly, we find that a majority of genes are under the direct control of the differentiation-inducing stimulus. CONCLUSIONS: Together, these results demonstrate WASABI versatility and ability to tackle some general gene regulatory networks inference issues. It is our hope that WASABI will prove useful in helping biologists to fully exploit the power of time-stamped single-cell data. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-019-2798-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6498543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64985432019-05-09 WASABI: a dynamic iterative framework for gene regulatory network inference Bonnaffoux, Arnaud Herbach, Ulysse Richard, Angélique Guillemin, Anissa Gonin-Giraud, Sandrine Gros, Pierre-Alexis Gandrillon, Olivier BMC Bioinformatics Research Article BACKGROUND: Inference of gene regulatory networks from gene expression data has been a long-standing and notoriously difficult task in systems biology. Recently, single-cell transcriptomic data have been massively used for gene regulatory network inference, with both successes and limitations. RESULTS: In the present work we propose an iterative algorithm called WASABI, dedicated to inferring a causal dynamical network from time-stamped single-cell data, which tackles some of the limitations associated with current approaches. We first introduce the concept of waves, which posits that the information provided by an external stimulus will affect genes one-by-one through a cascade, like waves spreading through a network. This concept allows us to infer the network one gene at a time, after genes have been ordered regarding their time of regulation. We then demonstrate the ability of WASABI to correctly infer small networks, which have been simulated in silico using a mechanistic model consisting of coupled piecewise-deterministic Markov processes for the proper description of gene expression at the single-cell level. We finally apply WASABI on in vitro generated data on an avian model of erythroid differentiation. The structure of the resulting gene regulatory network sheds a new light on the molecular mechanisms controlling this process. In particular, we find no evidence for hub genes and a much more distributed network structure than expected. Interestingly, we find that a majority of genes are under the direct control of the differentiation-inducing stimulus. CONCLUSIONS: Together, these results demonstrate WASABI versatility and ability to tackle some general gene regulatory networks inference issues. It is our hope that WASABI will prove useful in helping biologists to fully exploit the power of time-stamped single-cell data. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-019-2798-1) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-02 /pmc/articles/PMC6498543/ /pubmed/31046682 http://dx.doi.org/10.1186/s12859-019-2798-1 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Bonnaffoux, Arnaud Herbach, Ulysse Richard, Angélique Guillemin, Anissa Gonin-Giraud, Sandrine Gros, Pierre-Alexis Gandrillon, Olivier WASABI: a dynamic iterative framework for gene regulatory network inference |
title | WASABI: a dynamic iterative framework for gene regulatory network inference |
title_full | WASABI: a dynamic iterative framework for gene regulatory network inference |
title_fullStr | WASABI: a dynamic iterative framework for gene regulatory network inference |
title_full_unstemmed | WASABI: a dynamic iterative framework for gene regulatory network inference |
title_short | WASABI: a dynamic iterative framework for gene regulatory network inference |
title_sort | wasabi: a dynamic iterative framework for gene regulatory network inference |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6498543/ https://www.ncbi.nlm.nih.gov/pubmed/31046682 http://dx.doi.org/10.1186/s12859-019-2798-1 |
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