Evidence map›Paper›PMID 37626282›Full record

ArticleBMC bioinformatics2023

Predicting weighted unobserved nodes in a regulatory network using answer set programming.

Sophie Le Bars, Mathieu Bolteau, Jérémie Bourdon, Carito Guziolowski

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Article in BMC bioinformatics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Sophie Le BarsÉcole Centrale Nantes, CNRS, LS2N, UMR 6004, Nantes Université, Nantes, 44000, France. sophie.lebars1@gmail.com.ORCID http://orcid.org/0000-0002-2173-7744
Mathieu BolteauÉcole Centrale Nantes, CNRS, LS2N, UMR 6004, Nantes Université, Nantes, 44000, France.
Jérémie BourdonÉcole Centrale Nantes, CNRS, LS2N, UMR 6004, Nantes Université, Nantes, 44000, France.
Carito GuziolowskiÉcole Centrale Nantes, CNRS, LS2N, UMR 6004, Nantes Université, Nantes, 44000, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe impact of a perturbation, over-expression, or repression of a key node on an organism, can be modelled based on a regulatory and/or metabolic network. Integration of these two networks could improve our global understanding of biological mechanisms triggered by a perturbation. This study focuses on improving the modelling of the regulatory network to facilitate a possible integration with the metabolic network. Previously proposed methods that study this problem fail to deal with a real-size regulatory network, computing predictions sensitive to perturbation and quantifying the predicted species behaviour more finely.

resultsTo address previously mentioned limitations, we develop a new method based on Answer Set Programming, MajS. It takes a regulatory network and a discrete partial set of observations as input. MajS tests the consistency between the input data, proposes minimal repairs on the network to establish consistency, and finally computes weighted and signed predictions over the network species. We tested MajS by comparing the HIF-1 signalling pathway with two gene-expression datasets. Our results show that MajS can predict 100% of unobserved species. When comparing MajS with two similar (discrete and quantitative) tools, we observed that compared with the discrete tool, MajS proposes a better coverage of the unobserved species, is more sensitive to system perturbations, and proposes predictions closer to real data. Compared to the quantitative tool, MajS provides more refined discrete predictions that agree with the dynamic proposed by the quantitative tool.

conclusionsMajS is a new method to test the consistency between a regulatory network and a dataset that provides computational predictions on unobserved network species. It provides fine-grained discrete predictions by outputting the weight of the predicted sign as a piece of additional information. MajS' output, thanks to its weight, could easily be integrated with metabolic network modelling.

Indexed as

Signal TransductionGene ExpressionAnswer set programmingOMIC data integrationRegulatory and metabolic models integrationRegulatory network

Identifiers

PMID37626282
PMCPMC10463596

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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.