Evidence map›Paper›PMID 26772805›Full record

ArticleBMC bioinformatics2016

Deciphering transcriptional regulations coordinating the response to environmental changes.

Vicente Acuña, Andrés Aravena, Carito Guziolowski, Damien Eveillard, Anne Siegel, Alejandro Maass

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 100% of its field
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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Integration of Biological Networks forFrontiers in molecular biosciences · 2019
    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

6 authors at 5 institutions in 3 countries.

Vicente AcuñaCenter for Mathematical Modeling (UMI-CNRS 2807), Universidad de Chile, Santiago, Chile. viacuna@dim.uchile.cl.
Andrés AravenaDepartment of Molecular Biology and Genetics, Istanbul University, Istanbul, Turkey. andres.aravena@istanbul.edu.tr.
Carito GuziolowskiIRCCyN (UMR CNRS 6597), École Centrale de Nantes, Nantes, France. carito.guziolowski@irccyn.ec-nantes.fr.
Damien EveillardLINA (UMR CNRS 6241), Université de Nantes, École des Mines de Nantes, Nantes, France. damien.eveillard@univ-nantes.fr.
Anne SiegelIRISA Project Dyliss (UMR CNRS 6074), Université de Rennes 1, Rennes, France. anne.siegel@irisa.fr.
Alejandro MaassCenter for Mathematical Modeling (UMI-CNRS 2807), Universidad de Chile, Santiago, Chile. amaass@dim.uchile.cl.
University of Chile · CLÉcole Centrale de Nantes · FRInstitut de Recherche en Informatique et Systèmes Aléatoires · FRIstanbul University · TRNantes Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGene co-expression evidenced as a response to environmental changes has shown that transcriptional activity is coordinated, which pinpoints the role of transcriptional regulatory networks (TRNs). Nevertheless, the prediction of TRNs based on the affinity of transcription factors (TFs) with binding sites (BSs) generally produces an over-estimation of the observable TF/BS relations within the network and therefore many of the predicted relations are spurious.

resultsWe present LOMBARDE, a bioinformatics method that extracts from a TRN determined from a set of predicted TF/BS affinities a subnetwork explaining a given set of observed co-expressions by choosing the TFs and BSs most likely to be involved in the co-regulation. LOMBARDE solves an optimization problem which selects confident paths within a given TRN that join a putative common regulator with two co-expressed genes via regulatory cascades. To evaluate the method, we used public data of Escherichia coli to produce a regulatory network that explained almost all observed co-expressions while using only 19 % of the input TF/BS affinities but including about 66 % of the independent experimentally validated regulations in the input data. When all known validated TF/BS affinities were integrated into the input data the precision of LOMBARDE increased significantly. The topological characteristics of the subnetwork that was obtained were similar to the characteristics described for known validated TRNs.

conclusionsLOMBARDE provides a useful modeling scheme for deciphering the regulatory mechanisms that underlie the phenotypic responses of an organism to environmental challenges. The method can become a reliable tool for further research on genome-scale transcriptional regulation studies.

Indexed as

EnvironmentGene Expression RegulationGene Regulatory NetworksTranscription, GeneticComputational BiologyEscherichia coliTranscription FactorsTranscription Factors

Identifiers

PMID26772805
PMCPMC4715341
OpenAlexW2248975504

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.