Evidence map›Paper›PMID 7490289›Full record

ArticleThe Journal of cell biology1995

Saccharomyces cerevisiae cells execute a default pathway to select a mate in the absence of pheromone gradients.

R Dorer, P M Pryciak, L H Hartwell

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
5.3field-weighted citation impact, top 3% 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

53 citing papers in PubMed, 108 citations in OpenAlex.

  1. Article
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  4. Article
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  6. Article
  7. Gamete signalling underlies the evolution of mating types and their number.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2016
    Article
  8. Article
  9. Article
  10. Cell biology of yeast zygotes, from genesis to budding.Biochimica et biophysica acta · 2015
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Chemical gradients and chemotropism in yeast.Cold Spring Harbor perspectives in biology · 2009
    Review
  20. 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

3 authors at 1 institution in 1 country.

R DorerDepartment of Genetics, University of Washington, Seattle 98195-7360, USA.
P M Pryciak
L H Hartwell
University of Washington · US

Funding

University of Washington Medical Scientist Training Program: MD/PhDT32GM007266 · NIGMS · UNIVERSITY OF WASHINGTON · PI HORWITZ, MARSHALL S. · 1985 to 2023
$30.4M
TRAINING PROGRAM IN GENETICS GENERAL AND MEDICALT32GM007735 · NIGMS · UNIVERSITY OF WASHINGTON · PI THOMAS, JAMES H · 1985 to 2009
$3.8M
NIGMS NIH HHS GM07266NIGMS NIH HHS GM61-4590NIGMS NIH HHS T32GM-07735
6 · The paper itself

Abstract

During conjugation, haploid S. cerevisiae cells find one another by polarizing their growth toward each other along gradients of pheromone (chemotropism). We demonstrate that yeast cells exhibit a second mating behavior: when their receptors are saturated with pheromone, wild-type a cells execute a default pathway and select a mate at random. These matings are less efficient than chemotropic matings, are induced by the same dose of pheromone that induces shmoo formation, and appear to use a site near the incipient bud site for polarization. We show that the SPA2 gene is specifically required for the default pathway: spa2 delta mutants cannot mate if pheromone concentrations are high and gradients are absent, but can mate if gradients are present. ste2 delta, sst2 delta, and far1 delta mutants are chemotropism-defective and therefore must choose a mate by using a default pathway; consistent with this deduction, these strains require SPA2 to mate. In addition, our results suggest that far1 mutants are chemotropism-defective because their mating polarity is fixed at the incipient bud site, suggesting that the FAR1 gene is required for inhibiting the use of the incipient bud site during chemotropic mating. These observations reveal a molecular relationship between the mating and budding polarity pathways.

Indexed as

Cell Cycle ProteinsGTPase-Activating ProteinsGTP-Binding Protein beta SubunitsHeterotrimeric GTP-Binding ProteinsRepressor ProteinsSaccharomyces cerevisiae ProteinsCell CycleCell PolarityChemoreceptor CellsChemotactic FactorsCyclin-Dependent Kinase Inhibitor ProteinsCytoskeletal ProteinsFungal ProteinsGene DeletionGenes, FungalGTP-Binding ProteinsCell Cycle ProteinsChemotactic FactorsCyclin-Dependent Kinase Inhibitor ProteinsCytoskeletal ProteinsFAR1 protein, S cerevisiaeFungal ProteinsFUS1 protein, S cerevisiaeGTPase-Activating ProteinsGTP-Binding Protein beta SubunitsGTP-Binding ProteinsHeterotrimeric GTP-Binding ProteinsMembrane ProteinsPheromonesRepressor ProteinsRGS ProteinsSaccharomyces cerevisiae ProteinsSPA2 protein, S cerevisiaeSST2 protein, S cerevisiaeSte4 protein, S cerevisiae

Identifiers

PMID7490289
PMCPMC2200002
OpenAlexW2085816650

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.