Evidence map›Paper›PMID 25340401›Full record

ArticlePLoS genetics2014

Licensing of yeast centrosome duplication requires phosphoregulation of sfi1.

Jennifer S Avena, Shannon Burns, Zulin Yu, Christopher C Ebmeier, William M Old, Sue L Jaspersen, Mark Winey

Abstract read
In one paragraph

Article in PLoS genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Article
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  8. The Multiple Roles of the Cdc14 Phosphatase in Cell Cycle Control.International journal of molecular sciences · 2020
    Review
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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

7 authors.

Jennifer S AvenaMolecular, Cellular, and Developmental Biology, University of Colorado Boulder, Boulder, Colorado, United States of America.
Shannon BurnsStowers Institute for Medical Research, Kansas City, Missouri, United States of America.
Zulin YuStowers Institute for Medical Research, Kansas City, Missouri, United States of America.
Christopher C EbmeierMolecular, Cellular, and Developmental Biology, University of Colorado Boulder, Boulder, Colorado, United States of America.
William M OldMolecular, Cellular, and Developmental Biology, University of Colorado Boulder, Boulder, Colorado, United States of America.
Sue L JaspersenStowers Institute for Medical Research, Kansas City, Missouri, United States of America; Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, Kansas, United States of America.
Mark WineyMolecular, Cellular, and Developmental Biology, University of Colorado Boulder, Boulder, Colorado, United States of America.

Funding

Colorado Clinical and Translational Sciences InstituteUL1TR001082 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$48.0M
MOLECULAR BIOLOGYT32GM007135 · NIGMS · UNIVERSITY OF COLORADO AT BOULDER · PI KRAUTER, KENNETH S · 1985 to 2012
$5.7M
Role of MPSI Kinase and Yeast Spindle Pole CycleR01GM051312 · NIGMS · UNIVERSITY OF COLORADO AT BOULDER · PI WINEY, MARK · 1994 to 2015
$5.1M
NCATS NIH HHS UL1 TR001082NIGMS NIH HHS 5 T32 GM007135NIGMS NIH HHS R01 GM051312NIGMS NIH HHS R01 GM51312NIGMS NIH HHS T32 GM007135
6 · The paper itself

Abstract

Duplication of centrosomes once per cell cycle is essential for bipolar spindle formation and genome maintenance and is controlled in part by cyclin-dependent kinases (Cdks). Our study identifies Sfi1, a conserved component of centrosomes, as the first Cdk substrate required to restrict centrosome duplication to once per cell cycle. We found that reducing Cdk1 phosphorylation by changing Sfi1 phosphorylation sites to nonphosphorylatable residues leads to defects in separation of duplicated spindle pole bodies (SPBs, yeast centrosomes) and to inappropriate SPB reduplication during mitosis. These cells also display defects in bipolar spindle assembly, chromosome segregation, and growth. Our findings lead to a model whereby phosphoregulation of Sfi1 by Cdk1 has the dual function of promoting SPB separation for spindle formation and preventing premature SPB duplication. In addition, we provide evidence that the protein phosphatase Cdc14 has the converse role of activating licensing, likely via dephosphorylation of Sfi1.

Indexed as

CentrosomeCDC2 Protein KinaseCell Cycle ProteinsChromosome DuplicationChromosome SegregationMitosisPhosphorylationProtein Tyrosine PhosphatasesRepressor ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSpindle ApparatusSpindle Pole BodiesCDC14 protein, S cerevisiaeCDC2 Protein KinaseCell Cycle ProteinsProtein Tyrosine PhosphatasesRepressor ProteinsSaccharomyces cerevisiae ProteinsSFI1 protein, S cerevisiae

Identifiers

PMID25340401
PMCPMC4207612

What OpenQuestion holds

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LicenceCC BY
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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.