Evidence map›Paper›PMID 26241051›Full record

ArticlePloS one2015

Phosphatidylcholine Supply to Peroxisomes of the Yeast Saccharomyces cerevisiae.

Vid V Flis, Ariane Fankl, Claudia Ramprecht, Günther Zellnig, Erich Leitner, Albin Hermetter, Günther Daum

Erratum issuedOpen access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Determinants of Peroxisome Membrane Dynamics.Frontiers in physiology · 2022
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Pex35 is a regulator of peroxisome abundance.Journal of cell science · 2017
    Article
  11. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Vid V FlisInstitute of Biochemistry, Graz University of Technology, NAWI Graz, Graz, Austria.
Ariane FanklInstitute of Biochemistry, Graz University of Technology, NAWI Graz, Graz, Austria.
Claudia RamprechtInstitute of Biochemistry, Graz University of Technology, NAWI Graz, Graz, Austria.
Günther ZellnigInstitute of Plant Sciences, University of Graz, NAWI Graz, Graz, Austria.
Erich LeitnerInstitute of Analytical Chemistry and Food Technology, Graz University of Technology, NAWI Graz, Graz, Austria.
Albin HermetterInstitute of Biochemistry, Graz University of Technology, NAWI Graz, Graz, Austria.
Günther DaumInstitute of Biochemistry, Graz University of Technology, NAWI Graz, Graz, Austria.
Graz University of Technology · ATNawi Graz · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the yeast Saccharomyces cerevisiae, phosphatidylcholine (PC), the major phospholipid (PL) of all organelle membranes, is synthesized via two different pathways. Methylation of phosphatidylethanolamine (PE) catalyzed by the methyl transferases Cho2p/Pem1p and Opi3p/Pem2p as well as incorporation of choline through the CDP (cytidine diphosphate)-choline branch of the Kennedy pathway lead to PC formation. To determine the contribution of these two pathways to the supply of PC to peroxisomes (PX), yeast mutants bearing defects in the two pathways were cultivated under peroxisome inducing conditions, i.e. in the presence of oleic acid, and subjected to biochemical and cell biological analyses. Phenotype studies revealed compromised growth of both the cho20Δopi3Δ (mutations in the methylation pathway) and the cki1Δdpl1Δeki1Δ (mutations in the CDP-choline pathway) mutant when grown on oleic acid. Analysis of peroxisomes from the two mutant strains showed that both pathways produce PC for the supply to peroxisomes, although the CDP-choline pathway seemed to contribute with higher efficiency than the methylation pathway. Changes in the peroxisomal lipid pattern of mutants caused by defects in the PC biosynthetic pathways resulted in changes of membrane properties as shown by anisotropy measurements with fluorescent probes. In summary, our data define the origin of peroxisomal PC and demonstrate the importance of PC for peroxisome membrane formation and integrity.

Indexed as

Cytidine Diphosphate CholineFluorescence PolarizationFungal ProteinsIntracellular MembranesMembrane FluidityMethylationMicroscopy, ElectronMicrosomesMitochondriaMutationPeroxisomesPhosphatidylcholinesPhospholipidsSaccharomyces cerevisiaeSterolsCytidine Diphosphate CholineFungal ProteinsPhosphatidylcholinesPhospholipidsSterols

Identifiers

PMID26241051
PMCPMC4524607
OpenAlexW2261149784

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.