Evidence map›Paper›PMID 26020510›Full record

ArticlePLoS computational biology2015

Experimental and computational analysis of a large protein network that controls fat storage reveals the design principles of a signaling network.

Bader Al-Anzi, Patrick Arpp, Sherif Gerges, Christopher Ormerod, Noah Olsman, Kai Zinn

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2015. 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
0.8field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. A Guide to Conquer the Biological Network Era Using Graph Theory.Frontiers in bioengineering and biotechnology · 2020
    Review
  3. Article
  4. Review
  5. 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 2 institutions in 1 country.

Bader Al-AnziDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, California, United States of America.
Patrick ArppDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, California, United States of America.
Sherif GergesDepartment of Molecular Biology, Princeton University, Princeton, New Jersey, United States of America.
Christopher OrmerodDivision of Physics, Mathematics, and Astronomy, California Institute of Technology, Pasadena, California, United States of America.
Noah OlsmanControl and Dynamical Systems Option, Division of Engineering and Applied Sciences, California Institute of Technology, Pasadena, California, United States of America.
Kai ZinnDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, California, United States of America.
California Institute of Technology · USPrinceton University · US

Funding

Identifying New Regulators of Leptin-Like Signaling in Drosophila Brain NeuronsR21NS083874 · NINDS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI AL-ANZI, BADER F, ZINN, KAI G · 2013 to 2014
$456k
NINDS NIH HHS R21 NS083874
6 · The paper itself

Abstract

An approach combining genetic, proteomic, computational, and physiological analysis was used to define a protein network that regulates fat storage in budding yeast (Saccharomyces cerevisiae). A computational analysis of this network shows that it is not scale-free, and is best approximated by the Watts-Strogatz model, which generates "small-world" networks with high clustering and short path lengths. The network is also modular, containing energy level sensing proteins that connect to four output processes: autophagy, fatty acid synthesis, mRNA processing, and MAP kinase signaling. The importance of each protein to network function is dependent on its Katz centrality score, which is related both to the protein's position within a module and to the module's relationship to the network as a whole. The network is also divisible into subnetworks that span modular boundaries and regulate different aspects of fat metabolism. We used a combination of genetics and pharmacology to simultaneously block output from multiple network nodes. The phenotypic results of this blockage define patterns of communication among distant network nodes, and these patterns are consistent with the Watts-Strogatz model.

Indexed as

AlgorithmsCluster AnalysisComputational BiologyComputer SimulationFatty AcidsGene DeletionMAP Kinase Signaling SystemModels, GeneticModels, TheoreticalMutationPhenotypeProteinsProteomeReproducibility of ResultsSaccharomyces cerevisiaeSirolimusFatty AcidsProteinsProteomeSirolimus

Identifiers

PMID26020510
PMCPMC4447291
OpenAlexW1492121683

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.