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


Journal

BMC bioinformatics
ISSN: 1471-2105
Titre abrégé: BMC Bioinformatics
Pays: England
ID NLM: 100965194

Informations de publication

Date de publication:
21 Jan 2020
Historique:
received: 18 06 2019
accepted: 30 12 2019
entrez: 23 1 2020
pubmed: 23 1 2020
medline: 9 4 2020
Statut: epublish

Résumé

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. 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. 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. 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.

Sections du résumé

BACKGROUND 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 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 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 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.

Identifiants

pubmed: 31964336
doi: 10.1186/s12859-019-3337-9
pii: 10.1186/s12859-019-3337-9
pmc: PMC6975020
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

23

Subventions

Organisme : Bundesministerium für Bildung und Forschung
ID : 031A600A/B
Organisme : Vetenskapsrådet
ID : 2014-6545
Organisme : Fonds National de la Recherche Luxembourg
ID : NTER/SYSAPP/14/05
Organisme : SystemsX (CH)
ID : ERASysAPP
Organisme : Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
ID : 205321 173020
Organisme : Fondecyt
ID : 1161007

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Auteurs

Antoine Buetti-Dinh (A)

Institute of Computational Science, Faculty of Informatics, Università della Svizzera Italiana, Via Giuseppe Buffi 13, Lugano, CH-6900, Switzerland. antoine.buetti@sib.swiss.
Swiss Institute of Bioinformatics, Quartier Sorge - Batiment Genopode, Lausanne, CH-1015, Switzerland. antoine.buetti@sib.swiss.
Department of Chemistry and Biomedical Sciences, Linnæus University, Hus Vita, Kalmar, SE-391 82, Sweden. antoine.buetti@sib.swiss.
Linnæus University Centre for Biomaterials Chemistry, Linnæus University, Hus Vita, Kalmar, SE-391 82, Sweden. antoine.buetti@sib.swiss.
Centre for Ecology and Evolution in Microbial Model Systems, Linnæus University, Hus Vita, Kalmar, SE-391 82, Sweden. antoine.buetti@sib.swiss.

Malte Herold (M)

Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Belvaux, Luxembourg.

Stephan Christel (S)

Centre for Ecology and Evolution in Microbial Model Systems, Linnæus University, Hus Vita, Kalmar, SE-391 82, Sweden.

Mohamed El Hajjami (M)

Center for Marine and Molecular Biotechnology, QNLM, Qingdao, China.

Francesco Delogu (F)

Faculty of Chemistry, Biotechnology and Food Science, Norwegian University of Life Sciences, Oslo, Norway.

Olga Ilie (O)

Institute of Computational Science, Faculty of Informatics, Università della Svizzera Italiana, Via Giuseppe Buffi 13, Lugano, CH-6900, Switzerland.
Swiss Institute of Bioinformatics, Quartier Sorge - Batiment Genopode, Lausanne, CH-1015, Switzerland.

Sören Bellenberg (S)

Centre for Ecology and Evolution in Microbial Model Systems, Linnæus University, Hus Vita, Kalmar, SE-391 82, Sweden.

Paul Wilmes (P)

Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Belvaux, Luxembourg.

Ansgar Poetsch (A)

Plant Biochemistry, Ruhr University Bochum, Bochum, Germany.
Center for Marine and Molecular Biotechnology, QNLM, Qingdao, China.
College of Marine Life Sciences, Ocean University of China, Qingdao, China.

Wolfgang Sand (W)

Faculty of Chemistry, Essen, Germany.
College of Environmental Science and Engineering, Donghua University, Shanghai, People's Republic of China.
Mining Academy and Technical University Freiberg, Freiberg, Germany.

Mario Vera (M)

Institute for Biological and Medical Engineering. Schools of Engineering, Medicine & Biological Sciences, Pontificia Universidad Católica de Chile, Santiago, Chile.
Department of Hydraulic & Environmental Engineering, Pontificia Universidad Católica de Chile, Santiago, Chile.

Igor V Pivkin (IV)

Institute of Computational Science, Faculty of Informatics, Università della Svizzera Italiana, Via Giuseppe Buffi 13, Lugano, CH-6900, Switzerland.
Swiss Institute of Bioinformatics, Quartier Sorge - Batiment Genopode, Lausanne, CH-1015, Switzerland.

Ran Friedman (R)

Department of Chemistry and Biomedical Sciences, Linnæus University, Hus Vita, Kalmar, SE-391 82, Sweden.
Linnæus University Centre for Biomaterials Chemistry, Linnæus University, Hus Vita, Kalmar, SE-391 82, Sweden.

Mark Dopson (M)

Centre for Ecology and Evolution in Microbial Model Systems, Linnæus University, Hus Vita, Kalmar, SE-391 82, Sweden.

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