Evidence map›Paper›PMID 38129786›Full record

ArticleBMC bioinformatics2023

ICON-GEMs: integration of co-expression network in genome-scale metabolic models, shedding light through systems biology.

Thummarat Paklao, Apichat Suratanee, Kitiporn Plaimas

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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. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Thummarat PaklaoAdvanced Virtual and Intelligent Computing (AVIC) Center, Department of Mathematics and Computer Science, Faculty of Science, Chulalongkorn University, Bangkok, 10330, Thailand.
Apichat SurataneeDepartment of Mathematics, Faculty of Applied Science, King Mongkut's University of Technology North Bangkok, Bangkok, 10800, Thailand.
Kitiporn PlaimasAdvanced Virtual and Intelligent Computing (AVIC) Center, Department of Mathematics and Computer Science, Faculty of Science, Chulalongkorn University, Bangkok, 10330, Thailand. kitiporn.p@chula.ac.th.

Funding

National Science, Research and Innovation Fund (NSRF), and King Mongkut's University of Technology North Bangkok KMUTNB-FF-66-08
6 · The paper itself

Abstract

backgroundFlux Balance Analysis (FBA) is a key metabolic modeling method used to simulate cellular metabolism under steady-state conditions. Its simplicity and versatility have led to various strategies incorporating transcriptomic and proteomic data into FBA, successfully predicting flux distribution and phenotypic results. However, despite these advances, the untapped potential lies in leveraging gene-related connections like co-expression patterns for valuable insights.

resultsTo fill this gap, we introduce ICON-GEMs, an innovative constraint-based model to incorporate gene co-expression network into the FBA model, facilitating more precise determination of flux distributions and functional pathways. In this study, transcriptomic data from both Escherichia coli and Saccharomyces cerevisiae were integrated into their respective genome-scale metabolic models. A comprehensive gene co-expression network was constructed as a global view of metabolic mechanism of the cell. By leveraging quadratic programming, we maximized the alignment between pairs of reaction fluxes and the correlation of their corresponding genes in the co-expression network. The outcomes notably demonstrated that ICON-GEMs outperformed existing methodologies in predictive accuracy. Flux variabilities over subsystems and functional modules also demonstrate promising results. Furthermore, a comparison involving different types of biological networks, including protein-protein interactions and random networks, reveals insights into the utilization of the co-expression network in genome-scale metabolic engineering.

conclusionICON-GEMs introduce an innovative constrained model capable of simultaneous integration of gene co-expression networks, ready for board application across diverse transcriptomic data sets and multiple organisms. It is freely available as open-source at https://github.com/ThummaratPaklao/ICOM-GEMs.git .

Indexed as

ProteomicsSystems BiologyEscherichia coliGene Expression ProfilingGenomeMetabolic EngineeringMetabolic Flux AnalysisMetabolic Networks and PathwaysModels, BiologicalSaccharomyces cerevisiaeConstraint-based approachEscherichia coliFlux balance analysis (FBA)Gene co-expression networkGenome-scale metabolic modelMetabolic engineeringMetabolic flux analysisQuadratic programmingSaccharomyces cerevisiaeTranscriptomic data

Identifiers

PMID38129786
PMCPMC10740312

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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.