Evidence map›Paper›PMID 19570912›Full record

ArticleMolecular biology of the cell2009

Distinct roles for key karyogamy proteins during yeast nuclear fusion.

Patricia Melloy, Shu Shen, Erin White, Mark D Rose

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Nuclear Fusion in Yeast and Plant Reproduction.Plants (Basel, Switzerland) · 2023
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Cell biology of yeast zygotes, from genesis to budding.Biochimica et biophysica acta · 2015
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
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  17. Article
  18. 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 2 institutions in 1 country.

Patricia MelloyDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA. mdrose@princeton.edu
Shu Shen
Erin White
Mark D Rose
Princeton University · USUniversity of Colorado Boulder · US

Funding

WORKSHOPS AND TRAINING FOR IMAGE ANALYSIS USING IMODP41RR000592 · NCRR · UNIVERSITY OF COLORADO AT BOULDER · PI BASS, PETER W. · 1985 to 2011
$11.9M
Mechanisms of Nuclear and Cell Fusion in YeastR01GM037739 · NIGMS · PRINCETON UNIVERSITY · PI ROSE, MARK DAVID · 1987 to 2016
$7.4M
ONCOLOGY: MOLECULAR BASIS OF CANCERT32CA009528 · NCI · PRINCETON UNIVERSITY · PI BROACH, JAMES R. · 1985 to 2010
$5.9M
Resolving the nuclear fusion steps during yeast matingF32GM069288 · NIGMS · PRINCETON UNIVERSITY · PI MELLOY, PATRICIA G · 2004 to 2006
$85k
NCI NIH HHS T32 CA009528NCRR NIH HHS P41 RR000592NCRR NIH HHS RR 00592NIGMS NIH HHS F32 GM069288NIGMS NIH HHS R01 GM037739NIGMS NIH HHS R01 GM37739
6 · The paper itself

Abstract

During yeast mating, cell fusion is followed by the congression and fusion of the two nuclei. Proteins required for nuclear fusion are found at the surface (Prm3p) and within the lumen (Kar2p, Kar5p, and Kar8p) of the nuclear envelope (NE). Electron tomography (ET) of zygotes revealed that mutations in these proteins block nuclear fusion with different morphologies, suggesting that they act in different steps of fusion. Specifically, prm3 zygotes were blocked before formation of membrane bridges, whereas kar2, kar5, and kar8 zygotes frequently contained them. Membrane bridges were significantly larger and occurred more frequently in kar2 and kar8, than in kar5 mutant zygotes. The kinetics of NE fusion in prm3, kar5, and kar8 mutants, measured by live-cell fluorescence microscopy, were well correlated with the size and frequency of bridges observed by ET. However the kar2 mutant was defective for transfer of NE lumenal GFP, but not diffusion within the lumen, suggesting that transfer was blocked at the NE fusion junction. These observations suggest that Prm3p acts before initiation of outer NE fusion, Kar5p may help dilation of the initial fusion pore, and Kar2p and Kar8p act after outer NE fusion, during inner NE fusion.

Indexed as

Saccharomyces cerevisiaeCell NucleusFluorescence Recovery After PhotobleachingFungal ProteinsGene Expression Regulation, FungalGreen Fluorescent ProteinsHSP70 Heat-Shock ProteinsMembrane FusionMembrane ProteinsMolecular ChaperonesMutationNuclear EnvelopeNuclear ProteinsSaccharomyces cerevisiae ProteinsFungal ProteinsGreen Fluorescent ProteinsHSP70 Heat-Shock ProteinsJEM1 protein, S cerevisiaeKAR2 protein, yeastKAR5 protein, S cerevisiaeMembrane ProteinsMolecular ChaperonesNuclear ProteinsPrm3 protein, S cerevisiaeSaccharomyces cerevisiae Proteins

Identifiers

PMID19570912
PMCPMC2735476
OpenAlexW1981767902

What OpenQuestion holds

Textmetadata
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.