Evidence map›Paper›PMID 21298086›Full record

ArticlePLoS genetics2011

Bub1-mediated adaptation of the spindle checkpoint.

Greicy H Goto, Ashutosh Mishra, Rashid Abdulle, Clive A Slaughter, Katsumi Kitagawa

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Review
  3. Loss of theMicrobiology spectrum · 2025
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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 at 2 institutions in 1 country.

Greicy H GotoCenter for Childhood Cancer, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio, United States of America.
Ashutosh Mishra
Rashid Abdulle
Clive A Slaughter
Katsumi Kitagawa
Nationwide Children's Hospital · USSt. Jude Children's Research Hospital · US

Funding

Kinetochore Function and Cell Cycle Progression RevisionR01GM068418 · NIGMS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI KITAGAWA, KATSUMI · 2003 to 2012
$2.5M
NIGMS NIH HHS GM68418NIGMS NIH HHS R01 GM068418
6 · The paper itself

Abstract

During cell division, the spindle checkpoint ensures accurate chromosome segregation by monitoring the kinetochore-microtubule interaction and delaying the onset of anaphase until each pair of sister chromosomes is properly attached to microtubules. The spindle checkpoint is deactivated as chromosomes start moving toward the spindles in anaphase, but the mechanisms by which this deactivation and adaptation to prolonged mitotic arrest occur remain obscure. Our results strongly suggest that Cdc28-mediated phosphorylation of Bub1 at T566 plays an important role for the degradation of Bub1 in anaphase, and the phosphorylation is required for adaptation of the spindle checkpoint to prolonged mitotic arrest.

Indexed as

Chromosome SegregationAnaphaseCDC28 Protein Kinase, S cerevisiaeG1 PhaseGenes, cdcKinetochoresMicrotubulesMitosisPhosphorylationProtein Serine-Threonine KinasesSaccharomyces cerevisiaeS PhaseSpindle ApparatusThreonineBub1 spindle checkpoint proteinCDC28 Protein Kinase, S cerevisiaeProtein Serine-Threonine KinasesThreonine

Identifiers

PMID21298086
PMCPMC3029250
OpenAlexW2017240584

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.