Evidence map›Paper›PMID 12486115›Full record

ArticleThe Journal of cell biology2002

Mps3p is a novel component of the yeast spindle pole body that interacts with the yeast centrin homologue Cdc31p.

Sue L Jaspersen, Thomas H Giddings, Mark Winey

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

91 citing papers in PubMed, 154 citations in OpenAlex.

  1. Review
  2. Review
  3. Yeast centrosomes act as organizing centers to promote Polo kinase-mediated adaptation to persistent DNA damage.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Nuclear Fusion in Yeast and Plant Reproduction.Plants (Basel, Switzerland) · 2023
    Article
  5. A Yeast Mitotic Tale for the Nucleus and the Vacuoles to Embrace.International journal of molecular sciences · 2023
    Review
  6. Article
  7. Article
  8. Review
  9. TheCells · 2021
    Review
  10. Article
  11. Article
  12. Review
  13. Evolution and Functional Divergence ofFrontiers in plant science · 2021
    Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article

31 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

3 authors at 1 institution in 1 country.

Sue L JaspersenDepartment of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder, CO 80309, USA.
Thomas H Giddings
Mark Winey
University of Colorado Boulder · US

Funding

Role of MPSI Kinase and Yeast Spindle Pole CycleR01GM051312 · NIGMS · UNIVERSITY OF COLORADO AT BOULDER · PI WINEY, MARK · 1994 to 2015
$5.1M
NIGMS NIH HHS GM51312NIGMS NIH HHS R01 GM051312
6 · The paper itself

Abstract

Accurate duplication of the Saccharomyces cerevisiae spindle pole body (SPB) is required for formation of a bipolar mitotic spindle. We identified mutants in SPB assembly by screening a temperature-sensitive collection of yeast for defects in SPB incorporation of a fluorescently marked integral SPB component, Spc42p. One SPB assembly mutant contained a mutation in a previously uncharacterized open reading frame that we call MPS3 (for monopolar spindle). mps3-1 mutants arrest in mitosis with monopolar spindles at the nonpermissive temperature, suggesting a defect in SPB duplication. Execution point experiments revealed that MPS3 function is required for the first step of SPB duplication in G1. Like cells containing mutations in two other genes required for this step of SPB duplication (CDC31 and KAR1), mps3-1 mutants arrest with a single unduplicated SPB that lacks an associated half-bridge. MPS3 encodes an essential integral membrane protein that localizes to the SPB half-bridge. Genetic interactions between MPS3 and CDC31 and binding of Cdc31p to Mps3p in vitro, as well as the fact that Cdc31p localization to the SPB is partially dependent on Mps3p function, suggest that one function for Mps3p during SPB duplication is to recruit Cdc31p, the yeast centrin homologue, to the half-bridge.

Indexed as

Amino Acid MotifsBlotting, WesternCalcium-Binding ProteinsCell Cycle ProteinsGreen Fluorescent ProteinsLuminescent ProteinsMembrane ProteinsMitosisModels, BiologicalMutationNuclear ProteinsPhenotypePlasmidsPrecipitin TestsProtein BindingSaccharomyces cerevisiaeCalcium-Binding ProteinsCDC31 protein, S cerevisiaeCell Cycle ProteinsGreen Fluorescent ProteinsLuminescent ProteinsMembrane ProteinsMps3 protein, S cerevisiaeNuclear ProteinsSaccharomyces cerevisiae Proteins

Identifiers

PMID12486115
PMCPMC2173979
OpenAlexW2149327250

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.