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Reverse engineering directed gene regulatory networks from transcriptomics and proteomics data of biomining bacterial communities with approximate Bayesian computation and steady-state signalling simulations

BACKGROUND: Network inference is an important aim of systems biology. It enables the transformation of OMICs datasets into biological knowledge. It consists of reverse engineering gene regulatory networks from OMICs data, such as RNAseq or mass spectrometry-based proteomics data, through computation...

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Autores principales: Buetti-Dinh, Antoine, Herold, Malte, Christel, Stephan, El Hajjami, Mohamed, Delogu, Francesco, Ilie, Olga, Bellenberg, Sören, Wilmes, Paul, Poetsch, Ansgar, Sand, Wolfgang, Vera, Mario, Pivkin, Igor V., Friedman, Ran, Dopson, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6975020/
https://www.ncbi.nlm.nih.gov/pubmed/31964336
http://dx.doi.org/10.1186/s12859-019-3337-9
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author Buetti-Dinh, Antoine
Herold, Malte
Christel, Stephan
El Hajjami, Mohamed
Delogu, Francesco
Ilie, Olga
Bellenberg, Sören
Wilmes, Paul
Poetsch, Ansgar
Sand, Wolfgang
Vera, Mario
Pivkin, Igor V.
Friedman, Ran
Dopson, Mark
author_facet Buetti-Dinh, Antoine
Herold, Malte
Christel, Stephan
El Hajjami, Mohamed
Delogu, Francesco
Ilie, Olga
Bellenberg, Sören
Wilmes, Paul
Poetsch, Ansgar
Sand, Wolfgang
Vera, Mario
Pivkin, Igor V.
Friedman, Ran
Dopson, Mark
author_sort Buetti-Dinh, Antoine
collection PubMed
description BACKGROUND: Network inference is an important aim of systems biology. It enables the transformation of OMICs datasets into biological knowledge. It consists of reverse engineering gene regulatory networks from OMICs data, such as RNAseq or mass spectrometry-based proteomics data, through computational methods. This approach allows to identify signalling pathways involved in specific biological functions. The ability to infer causality in gene regulatory networks, in addition to correlation, is crucial for several modelling approaches and allows targeted control in biotechnology applications. METHODS: We performed simulations according to the approximate Bayesian computation method, where the core model consisted of a steady-state simulation algorithm used to study gene regulatory networks in systems for which a limited level of details is available. The simulations outcome was compared to experimentally measured transcriptomics and proteomics data through approximate Bayesian computation. RESULTS: The structure of small gene regulatory networks responsible for the regulation of biological functions involved in biomining were inferred from multi OMICs data of mixed bacterial cultures. Several causal inter- and intraspecies interactions were inferred between genes coding for proteins involved in the biomining process, such as heavy metal transport, DNA damage, replication and repair, and membrane biogenesis. The method also provided indications for the role of several uncharacterized proteins by the inferred connection in their network context. CONCLUSIONS: The combination of fast algorithms with high-performance computing allowed the simulation of a multitude of gene regulatory networks and their comparison to experimentally measured OMICs data through approximate Bayesian computation, enabling the probabilistic inference of causality in gene regulatory networks of a multispecies bacterial system involved in biomining without need of single-cell or multiple perturbation experiments. This information can be used to influence biological functions and control specific processes in biotechnology applications.
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spelling pubmed-69750202020-01-28 Reverse engineering directed gene regulatory networks from transcriptomics and proteomics data of biomining bacterial communities with approximate Bayesian computation and steady-state signalling simulations Buetti-Dinh, Antoine Herold, Malte Christel, Stephan El Hajjami, Mohamed Delogu, Francesco Ilie, Olga Bellenberg, Sören Wilmes, Paul Poetsch, Ansgar Sand, Wolfgang Vera, Mario Pivkin, Igor V. Friedman, Ran Dopson, Mark BMC Bioinformatics Research Article BACKGROUND: Network inference is an important aim of systems biology. It enables the transformation of OMICs datasets into biological knowledge. It consists of reverse engineering gene regulatory networks from OMICs data, such as RNAseq or mass spectrometry-based proteomics data, through computational methods. This approach allows to identify signalling pathways involved in specific biological functions. The ability to infer causality in gene regulatory networks, in addition to correlation, is crucial for several modelling approaches and allows targeted control in biotechnology applications. METHODS: We performed simulations according to the approximate Bayesian computation method, where the core model consisted of a steady-state simulation algorithm used to study gene regulatory networks in systems for which a limited level of details is available. The simulations outcome was compared to experimentally measured transcriptomics and proteomics data through approximate Bayesian computation. RESULTS: The structure of small gene regulatory networks responsible for the regulation of biological functions involved in biomining were inferred from multi OMICs data of mixed bacterial cultures. Several causal inter- and intraspecies interactions were inferred between genes coding for proteins involved in the biomining process, such as heavy metal transport, DNA damage, replication and repair, and membrane biogenesis. The method also provided indications for the role of several uncharacterized proteins by the inferred connection in their network context. CONCLUSIONS: The combination of fast algorithms with high-performance computing allowed the simulation of a multitude of gene regulatory networks and their comparison to experimentally measured OMICs data through approximate Bayesian computation, enabling the probabilistic inference of causality in gene regulatory networks of a multispecies bacterial system involved in biomining without need of single-cell or multiple perturbation experiments. This information can be used to influence biological functions and control specific processes in biotechnology applications. BioMed Central 2020-01-21 /pmc/articles/PMC6975020/ /pubmed/31964336 http://dx.doi.org/10.1186/s12859-019-3337-9 Text en © The Author(s) 2020 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
Buetti-Dinh, Antoine
Herold, Malte
Christel, Stephan
El Hajjami, Mohamed
Delogu, Francesco
Ilie, Olga
Bellenberg, Sören
Wilmes, Paul
Poetsch, Ansgar
Sand, Wolfgang
Vera, Mario
Pivkin, Igor V.
Friedman, Ran
Dopson, Mark
Reverse engineering directed gene regulatory networks from transcriptomics and proteomics data of biomining bacterial communities with approximate Bayesian computation and steady-state signalling simulations
title Reverse engineering directed gene regulatory networks from transcriptomics and proteomics data of biomining bacterial communities with approximate Bayesian computation and steady-state signalling simulations
title_full Reverse engineering directed gene regulatory networks from transcriptomics and proteomics data of biomining bacterial communities with approximate Bayesian computation and steady-state signalling simulations
title_fullStr Reverse engineering directed gene regulatory networks from transcriptomics and proteomics data of biomining bacterial communities with approximate Bayesian computation and steady-state signalling simulations
title_full_unstemmed Reverse engineering directed gene regulatory networks from transcriptomics and proteomics data of biomining bacterial communities with approximate Bayesian computation and steady-state signalling simulations
title_short Reverse engineering directed gene regulatory networks from transcriptomics and proteomics data of biomining bacterial communities with approximate Bayesian computation and steady-state signalling simulations
title_sort reverse engineering directed gene regulatory networks from transcriptomics and proteomics data of biomining bacterial communities with approximate bayesian computation and steady-state signalling simulations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6975020/
https://www.ncbi.nlm.nih.gov/pubmed/31964336
http://dx.doi.org/10.1186/s12859-019-3337-9
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