Evidence map›Paper›PMID 25584613›Full record

ReviewInternational journal of molecular sciences2015

Membrane trafficking in the yeast Saccharomyces cerevisiae model.

Serge Feyder, Johan-Owen De Craene, Séverine Bär, Dimitri L Bertazzi, Sylvie Friant

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing 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

79 citing papers in PubMed.

  1. Article
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  3. Review
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  9. Article
  10. Tailored UPRE2 variants for dynamic gene regulation in yeast.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. New Insights on the Uptake and Trafficking of Coenzyme Q.Antioxidants (Basel, Switzerland) · 2023
    Review
  17. Article
  18. Article
  19. Article
  20. Article

19 more citing papers are in PubMed but not listed here.

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

5 authors.

Serge FeyderDepartment of Molecular and Cellular Genetics, UMR7156, Université de Strasbourg and CNRS, 21 rue Descartes, Strasbourg 67084, France. sergefeyder@hotmail.com.
Johan-Owen De CraeneDepartment of Molecular and Cellular Genetics, UMR7156, Université de Strasbourg and CNRS, 21 rue Descartes, Strasbourg 67084, France. seahorse378@gmail.com.
Séverine BärDepartment of Molecular and Cellular Genetics, UMR7156, Université de Strasbourg and CNRS, 21 rue Descartes, Strasbourg 67084, France. sbar@unistra.fr.
Dimitri L BertazziDepartment of Molecular and Cellular Genetics, UMR7156, Université de Strasbourg and CNRS, 21 rue Descartes, Strasbourg 67084, France. dimitri.bertazzi@gmail.com.
Sylvie FriantDepartment of Molecular and Cellular Genetics, UMR7156, Université de Strasbourg and CNRS, 21 rue Descartes, Strasbourg 67084, France. s.friant@unistra.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The yeast Saccharomyces cerevisiae is one of the best characterized eukaryotic models. The secretory pathway was the first trafficking pathway clearly understood mainly thanks to the work done in the laboratory of Randy Schekman in the 1980s. They have isolated yeast sec mutants unable to secrete an extracellular enzyme and these SEC genes were identified as encoding key effectors of the secretory machinery. For this work, the 2013 Nobel Prize in Physiology and Medicine has been awarded to Randy Schekman; the prize is shared with James Rothman and Thomas Südhof. Here, we present the different trafficking pathways of yeast S. cerevisiae. At the Golgi apparatus newly synthesized proteins are sorted between those transported to the plasma membrane (PM), or the external medium, via the exocytosis or secretory pathway (SEC), and those targeted to the vacuole either through endosomes (vacuolar protein sorting or VPS pathway) or directly (alkaline phosphatase or ALP pathway). Plasma membrane proteins can be internalized by endocytosis (END) and transported to endosomes where they are sorted between those targeted for vacuolar degradation and those redirected to the Golgi (recycling or RCY pathway). Studies in yeast S. cerevisiae allowed the identification of most of the known effectors, protein complexes, and trafficking pathways in eukaryotic cells, and most of them are conserved among eukaryotes.

Indexed as

Cell MembraneEndocytosisEndosomesGolgi ApparatusMembrane ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSecretory VesiclesMembrane ProteinsSaccharomyces cerevisiae Proteins

Identifiers

PMID25584613
PMCPMC4307317

What OpenQuestion holds

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Registered trials

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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.