Evidence map›Paper›PMID 20459825›Full record

ArticleBMC systems biology2010

Evolution of metabolic network organization.

Aurélien Mazurie, Danail Bonchev, Benno Schwikowski, Gregory A Buck

Abstract read
In one paragraph

Article in BMC systems biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
–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

25 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. On the Origin of Biomolecular Networks.Frontiers in genetics · 2019
    Pooled it
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  16. Analysis of metabolic evolution in bacteria using whole-genome metabolic models.Journal of computational biology : a journal of computational molecular cell biology · 2013
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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

4 authors.

Aurélien MazurieInstitut Pasteur, Systems Biology Lab, Department of Genomes and Genetics, F-75015 Paris, France. ajmazurie@vcu.edu
Danail Bonchev
Benno Schwikowski
Gregory A Buck

Funding

Functional genomics of metacyclogenesis in T.cruziR01AI050196 · NIAID · VIRGINIA COMMONWEALTH UNIVERSITY · PI BUCK, GREGORY ALLEN · 2002 to 2006
$2.6M
Functional Genomics of Cryptosporidium parvumR01AI055347 · NIAID · TUFTS UNIVERSITY BOSTON · PI WIDMER, GIOVANNI · 2004 to 2007
$1.7M
NIAID NIH HHS R01AI050196NIAID NIH HHS R01AI055347
6 · The paper itself

Abstract

backgroundComparison of metabolic networks across species is a key to understanding how evolutionary pressures shape these networks. By selecting taxa representative of different lineages or lifestyles and using a comprehensive set of descriptors of the structure and complexity of their metabolic networks, one can highlight both qualitative and quantitative differences in the metabolic organization of species subject to distinct evolutionary paths or environmental constraints.

resultsWe used a novel representation of metabolic networks, termed network of interacting pathways or NIP, to focus on the modular, high-level organization of the metabolic capabilities of the cell. Using machine learning techniques we identified the most relevant aspects of cellular organization that change under evolutionary pressures. We considered the transitions from prokarya to eukarya (with a focus on the transitions among the archaea, bacteria and eukarya), from unicellular to multicellular eukarya, from free living to host-associated bacteria, from anaerobic to aerobic, as well as the acquisition of cell motility or growth in an environment of various levels of salinity or temperature. Intuitively, we expect organisms with more complex lifestyles to have more complex and robust metabolic networks. Here we demonstrate for the first time that such organisms are not only characterized by larger, denser networks of metabolic pathways but also have more efficiently organized cross communications, as revealed by subtle changes in network topology. These changes are unevenly distributed among metabolic pathways, with specific categories of pathways being promoted to more central locations as an answer to environmental constraints.

conclusionsCombining methods from graph theory and machine learning, we have shown here that evolutionary pressures not only affects gene and protein sequences, but also specific details of the complex wiring of functional modules in the cell. This approach allows the identification and quantification of those changes, and provides an overview of the evolution of intracellular systems.

Indexed as

Systems BiologyAlgorithmsArtificial IntelligenceBacteriaCell MovementComputational BiologyEvolution, MolecularGene Regulatory NetworksHumansMetabolic Networks and PathwaysModels, BiologicalProtein Interaction Mapping

Identifiers

PMID20459825
PMCPMC2876064

What OpenQuestion holds

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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.