Evidence map›Paper›PMID 30726152›Full record

ArticleMolecular biology of the cell2019

Cell cycle-dependent association of polo kinase Cdc5 with CENP-A contributes to faithful chromosome segregation in budding yeast.

Prashant K Mishra, Gudjon Olafsson, Lars Boeckmann, Timothy J Westlake, Ziad M Jowhar, Lauren E Dittman, Richard E Baker, Damien D'Amours, Peter H Thorpe, Munira A Basrai

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2019. 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
1.2field-weighted citation impact, top 24% 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, 23 citations in OpenAlex.

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  7. Unravelling the Transcriptional Response ofInternational journal of molecular sciences · 2024
    Article
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  9. Article
  10. Histone modification inComputational and structural biotechnology journal · 2023
    Review
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  13. Article
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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

10 authors at 4 institutions in 3 countries.

Prashant K MishraGenetics Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Gudjon OlafssonSchool of Biological and Chemical Sciences, Queen Mary University of London, London E1 4NS, United Kingdom.
Lars BoeckmannGenetics Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Timothy J WestlakeGenetics Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Ziad M JowharGenetics Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Lauren E DittmanGenetics Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Richard E BakerDepartment of Microbiology and Physiological Systems, University of Massachusetts Medical School, Worcester, MA 01655.
Damien D'AmoursDepartment of Cellular and Molecular Medicine, University of Ottawa, Ottawa, ON K1N 6N5, Canada.
Peter H ThorpeSchool of Biological and Chemical Sciences, Queen Mary University of London, London E1 4NS, United Kingdom.
Munira A BasraiGenetics Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
National Institutes of Health · USQueen Mary University of London · GBUniversity of Massachusetts Chan Medical School · USUniversity of Ottawa · CA

Funding

Molecular Determinants of Chromosome Transmission and Cell Cycle RegulationZIABC010822 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI BASRAI, MUNIRA · 2009 to 2025
$29.2M
Arthritis Research UK FC001003Medical Research Council MC_UP_A252_1027Wellcome Trust
6 · The paper itself

Abstract

Evolutionarily conserved polo-like kinase, Cdc5 (Plk1 in humans), associates with kinetochores during mitosis; however, the role of cell cycle-dependent centromeric ( CEN) association of Cdc5 and its substrates that exclusively localize to the kinetochore have not been characterized. Here we report that evolutionarily conserved CEN histone H3 variant, Cse4 (CENP-A in humans), is a substrate of Cdc5, and that the cell cycle-regulated association of Cse4 with Cdc5 is required for cell growth. Cdc5 contributes to Cse4 phosphorylation in vivo and interacts with Cse4 in mitotic cells. Mass spectrometry analysis of in vitro kinase assays showed that Cdc5 phosphorylates nine serine residues clustered within the N-terminus of Cse4. Strains with cse4-9SA exhibit increased errors in chromosome segregation, reduced levels of CEN-associated Mif2 and Mcd1/Scc1 when combined with a deletion of MCM21. Moreover, the loss of Cdc5 from the CEN chromatin contributes to defects in kinetochore integrity and reduction in CEN-associated Cse4. The cell cycle-regulated association of Cdc5 with Cse4 is essential for cell viability as constitutive association of Cdc5 with Cse4 at the kinetochore leads to growth defects. In summary, our results have defined a role for Cdc5-mediated Cse4 phosphorylation in faithful chromosome segregation.

Indexed as

Cell Cycle ProteinsCentromereCentromere Protein AChromatinChromosomal Proteins, Non-HistoneChromosome SegregationDNA-Binding ProteinsHistonesKinetochoresMitosisNuclear ProteinsPhosphorylationProtein Serine-Threonine KinasesSaccharomycesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsCDC5 protein, S cerevisiaeCell Cycle ProteinsCentromere Protein AChromatinChromosomal Proteins, Non-HistoneDNA-Binding ProteinsHistonesNuclear ProteinsPlo1 protein, S pombeProtein Serine-Threonine KinasesSaccharomyces cerevisiae ProteinsSchizosaccharomyces pombe Proteins

Identifiers

PMID30726152
PMCPMC6589903
OpenAlexW2913970608

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.