Evidence map›Paper›PMID 31964336›Full record

ArticleBMC bioinformatics2020

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

Antoine Buetti-Dinh, Malte Herold, Stephan Christel, Mohamed El Hajjami, Francesco Delogu, Olga Ilie, Sören Bellenberg, Paul Wilmes, Ansgar Poetsch, Wolfgang Sand and 4 more

Abstract read
In one paragraph

Article in BMC bioinformatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Modeling approaches for probing cross-feeding interactions in the human gut microbiome.Computational and structural biotechnology journal · 2022
    Review
  5. Article
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Antoine Buetti-DinhInstitute of Computational Science, Faculty of Informatics, Università della Svizzera Italiana, Via Giuseppe Buffi 13, Lugano, CH-6900, Switzerland. antoine.buetti@sib.swiss.ORCID http://orcid.org/0000-0002-6469-0296
Malte HeroldLuxembourg Centre for Systems Biomedicine, University of Luxembourg, Belvaux, Luxembourg.ORCID http://orcid.org/0000-0003-2627-0159
Stephan ChristelCentre for Ecology and Evolution in Microbial Model Systems, Linnæus University, Hus Vita, Kalmar, SE-391 82, Sweden.ORCID http://orcid.org/0000-0003-0021-2452
Mohamed El HajjamiCenter for Marine and Molecular Biotechnology, QNLM, Qingdao, China.
Francesco DeloguFaculty of Chemistry, Biotechnology and Food Science, Norwegian University of Life Sciences, Oslo, Norway.
Olga IlieInstitute of Computational Science, Faculty of Informatics, Università della Svizzera Italiana, Via Giuseppe Buffi 13, Lugano, CH-6900, Switzerland.
Sören BellenbergCentre for Ecology and Evolution in Microbial Model Systems, Linnæus University, Hus Vita, Kalmar, SE-391 82, Sweden.
Paul WilmesLuxembourg Centre for Systems Biomedicine, University of Luxembourg, Belvaux, Luxembourg.ORCID http://orcid.org/0000-0002-6478-2924
Ansgar PoetschPlant Biochemistry, Ruhr University Bochum, Bochum, Germany.
Wolfgang SandFaculty of Chemistry, Essen, Germany.
Mario VeraInstitute for Biological and Medical Engineering. Schools of Engineering, Medicine & Biological Sciences, Pontificia Universidad Católica de Chile, Santiago, Chile.ORCID http://orcid.org/0000-0002-1762-4421
Igor V PivkinInstitute of Computational Science, Faculty of Informatics, Università della Svizzera Italiana, Via Giuseppe Buffi 13, Lugano, CH-6900, Switzerland.
Ran FriedmanDepartment of Chemistry and Biomedical Sciences, Linnæus University, Hus Vita, Kalmar, SE-391 82, Sweden.ORCID http://orcid.org/0000-0001-8696-3104
Mark DopsonCentre for Ecology and Evolution in Microbial Model Systems, Linnæus University, Hus Vita, Kalmar, SE-391 82, Sweden.ORCID http://orcid.org/0000-0002-9622-3318

Funding

Bundesministerium für Bildung und Forschung 031A600A/BFondecyt 1161007Fonds National de la Recherche Luxembourg NTER/SYSAPP/14/05Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung 205321 173020SystemsX (CH) ERASysAPPVetenskapsrådet 2014-6545
6 · The paper itself

Abstract

backgroundNetwork 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.

methodsWe 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.

resultsThe 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.

conclusionsThe 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.

Indexed as

Gene Expression ProfilingGene Expression Regulation, BacterialGene Regulatory NetworksProteomicsAlgorithmsBacteriaBayes TheoremComputational BiologyComputer SimulationSignal TransductionSystems BiologyAcidophilesApproximate Bayesian computationBiological signalling simulationsBiominingGene regulatory networksMachine learningMultispecies bacterial community interactions

Identifiers

PMID31964336
PMCPMC6975020

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.