Evidence map›Paper›PMID 25626086›Full record

ArticlePLoS biology2015

Population diversification in a yeast metabolic program promotes anticipation of environmental shifts.

Ophelia S Venturelli, Ignacio Zuleta, Richard M Murray, Hana El-Samad

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 1 pooled it
6.8field-weighted citation impact, top 2% 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

60 citing papers in PubMed, 1 synthesis or guideline pooled it, 111 citations in OpenAlex.

  1. Pooled it
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  17. eLife · 2021
    Article
  18. Article
  19. Microbial metabolic noise.WIREs mechanisms of disease · 2021
    Review
  20. 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

4 authors at 3 institutions in 1 country.

Ophelia S VenturelliDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, California, United States of America; Department of Biochemistry and Biophysics, University of California San Francisco, San Francisco, California, United States of America; The California Institute for Quantitative Biosciences, University of California San Francisco, San Francisco, California, United States of America.
Ignacio ZuletaDepartment of Biochemistry and Biophysics, University of California San Francisco, San Francisco, California, United States of America; The California Institute for Quantitative Biosciences, University of California San Francisco, San Francisco, California, United States of America.
Richard M MurrayDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, California, United States of America.
Hana El-SamadDepartment of Biochemistry and Biophysics, University of California San Francisco, San Francisco, California, United States of America; The California Institute for Quantitative Biosciences, University of California San Francisco, San Francisco, California, United States of America.
QB3 · USCalifornia Institute of Technology · USUniversity of California, San Francisco · US

Funding

Rewiring Therapeutic Cells: User-Controlled T Cells and Stem CellsP50GM081879 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LIM, WENDELL A · 2010 to 2017
$19.0M
NIGMS NIH HHS P50 GM081879
6 · The paper itself

Abstract

Delineating the strategies by which cells contend with combinatorial changing environments is crucial for understanding cellular regulatory organization. When presented with two carbon sources, microorganisms first consume the carbon substrate that supports the highest growth rate (e.g., glucose) and then switch to the secondary carbon source (e.g., galactose), a paradigm known as the Monod model. Sequential sugar utilization has been attributed to transcriptional repression of the secondary metabolic pathway, followed by activation of this pathway upon depletion of the preferred carbon source. In this work, we demonstrate that although Saccharomyces cerevisiae cells consume glucose before galactose, the galactose regulatory pathway is activated in a fraction of the cell population hours before glucose is fully consumed. This early activation reduces the time required for the population to transition between the two metabolic programs and provides a fitness advantage that might be crucial in competitive environments.

Indexed as

Carbohydrate MetabolismComputer SimulationEnergy MetabolismGalactoseGene-Environment InteractionGene Expression Regulation, FungalGenes, FungalGlucoseModels, BiologicalSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsTranscriptional ActivationTranscription, GeneticGalactoseGlucoseSaccharomyces cerevisiae Proteins

Identifiers

PMID25626086
PMCPMC4307983
OpenAlexW2147333650

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.