Evidence map›Paper›PMID 29038751›Full record

ArticlePeerJ2017

Combining graph and flux-based structures to decipher phenotypic essential metabolites within metabolic networks.

Julie Laniau, Clémence Frioux, Jacques Nicolas, Caroline Baroukh, Maria-Paz Cortes, Jeanne Got, Camille Trottier, Damien Eveillard, Anne Siegel

Abstract read
In one paragraph

Article in PeerJ, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Opportunities at the Interface of Network Science and Metabolic Modeling.Frontiers in bioengineering and biotechnology · 2020
    Review
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

9 authors.

Julie LaniauInstitut de Recherche en Informatique et Systèmes Aléatoires, Centre National de la Recherche Scientifique, Rennes, France.
Clémence FriouxInstitut de Recherche en Informatique et Systèmes Aléatoires, Centre National de la Recherche Scientifique, Rennes, France.
Jacques NicolasInstitut de Recherche en Informatique et Systèmes Aléatoires, Centre National de la Recherche Scientifique, Rennes, France.
Caroline BaroukhLaboratoire des Interactions Plantes Micro-organismes, Institut National de la Recherche en Agonomie, Castanet-Tolosan, France.
Maria-Paz CortesCenter of Mathematical Modelling, Universidad de Chile, Santiago, Chile.
Jeanne GotInstitut de Recherche en Informatique et Systèmes Aléatoires, Centre National de la Recherche Scientifique, Rennes, France.
Camille TrottierDYLISS, Institut National de Recherche en Informatique et Automatique, Rennes, France.
Damien EveillardLaboratoire des Sciences du Numérique de Nantes, Université de Nantes, Nantes, France.
Anne SiegelInstitut de Recherche en Informatique et Systèmes Aléatoires, Centre National de la Recherche Scientifique, Rennes, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe emergence of functions in biological systems is a long-standing issue that can now be addressed at the cell level with the emergence of high throughput technologies for genome sequencing and phenotyping. The reconstruction of complete metabolic networks for various organisms is a key outcome of the analysis of these data, giving access to a global view of cell functioning. The analysis of metabolic networks may be carried out by simply considering the architecture of the reaction network or by taking into account the stoichiometry of reactions. In both approaches, this analysis is generally centered on the outcome of the network and considers all metabolic compounds to be equivalent in this respect. As in the case of genes and reactions, about which the concept of essentiality has been developed, it seems, however, that some metabolites play crucial roles in system responses, due to the cell structure or the internal wiring of the metabolic network.

resultsWe propose a classification of metabolic compounds according to their capacity to influence the activation of targeted functions (generally the growth phenotype) in a cell. We generalize the concept of essentiality to metabolites and introduce the concept of the

conclusionThe exhaustive study of phenotypic essential metabolites in six genome-scale metabolic models suggests that the combination and the comparison of graph, stoichiometry and optimal flux-based criteria allows some features of the metabolic network functionality to be deciphered by focusing on a small number of compounds. By considering the best combination of both graph-based and flux-based techniques, the

Indexed as

Answer Set ProgrammingConstraint-based analysisEssential metaboliteGraph-based analysisMetabolic networks

Identifiers

PMID29038751
PMCPMC5641430

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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.