Evidence map›Paper›PMID 23637466›Full record

ArticleMolecular biology of the cell2013

Phosphorylation of centromeric histone H3 variant regulates chromosome segregation in Saccharomyces cerevisiae.

Lars Boeckmann, Yoshimitsu Takahashi, Wei-Chun Au, Prashant K Mishra, John S Choy, Anthony R Dawson, May Y Szeto, Timothy J Waybright, Christopher Heger, Christopher McAndrew and 4 more

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

38 citing papers in PubMed, 54 citations in OpenAlex.

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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

14 authors at 2 institutions in 1 country.

Lars BoeckmannGenetics Branch, Center for Cancer Research, National Institutes of Health, Bethesda, MD 20892, USA.
Yoshimitsu Takahashi
Wei-Chun Au
Prashant K Mishra
John S Choy
Anthony R Dawson
May Y Szeto
Timothy J Waybright
Christopher Heger
Christopher McAndrew
Paul K Goldsmith
Timothy D Veenstra
Richard E Baker
Munira A Basrai
National Institutes of Health · USUniversity of Massachusetts Chan Medical School · US

Funding

Molecular Determinants of Chromosome Transmission and Cell Cycle RegulationZIABC010822 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI BASRAI, MUNIRA · 2009 to 2025
$29.2M
Intramural NIH HHS
6 · The paper itself

Abstract

The centromeric histone H3 variant (CenH3) is essential for chromosome segregation in eukaryotes. We identify posttranslational modifications of Saccharomyces cerevisiae CenH3, Cse4. Functional characterization of cse4 phosphorylation mutants shows growth and chromosome segregation defects when combined with kinetochore mutants okp1 and ame1. Using a phosphoserine-specific antibody, we show that the association of phosphorylated Cse4 with centromeres increases in response to defective microtubule attachment or reduced cohesion. We determine that evolutionarily conserved Ipl1/Aurora B contributes to phosphorylation of Cse4, as levels of phosphorylated Cse4 are reduced at centromeres in ipl1 strains in vivo, and in vitro assays show phosphorylation of Cse4 by Ipl1. Consistent with these results, we observe that a phosphomimetic cse4-4SD mutant suppresses the temperature-sensitive growth of ipl1-2 and Ipl1 substrate mutants dam1 spc34 and ndc80, which are defective for chromosome biorientation. Furthermore, cell biology approaches using a green fluorescent protein-labeled chromosome show that cse4-4SD suppresses chromosome segregation defects in dam1 spc34 strains. On the basis of these results, we propose that phosphorylation of Cse4 destabilizes defective kinetochores to promote biorientation and ensure faithful chromosome segregation. Taken together, our results provide a detailed analysis, in vivo and in vitro, of Cse4 phosphorylation and its role in promoting faithful chromosome segregation.

Indexed as

Chromosome SegregationAmino Acid SequenceAurora Kinase BAurora KinasesBinding SitesBlotting, WesternCell Cycle ProteinsCentromereChromatography, LiquidChromosomal Proteins, Non-HistoneDNA-Binding ProteinsKinetochoresMicrotubule-Associated ProteinsMolecular Sequence DataMutationNuclear ProteinsAme1 protein, S cerevisiaeAurora Kinase BAurora KinasesCell Cycle ProteinsChromosomal Proteins, Non-HistoneCSE4 protein, S cerevisiaeDAM1 protein, S cerevisiaeDNA-Binding ProteinsIPL1 protein, S cerevisiaeMicrotubule-Associated ProteinsNDC80 protein, S cerevisiaeNuclear ProteinsOkp1 protein, S cerevisiaeSaccharomyces cerevisiae ProteinsSpc34 protein, S cerevisiae

Identifiers

PMID23637466
PMCPMC3681705
OpenAlexW2115356248

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.