Evidence map›Paper›PMID 23283988›Full record

ArticleMolecular biology of the cell2013

Slk19 clusters kinetochores and facilitates chromosome bipolar attachment.

Daniel Richmond, Raed Rizkallah, Fengshan Liang, Myra M Hurt, Yanchang Wang

Abstract 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 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

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  11. Real-time dynamics ofJournal of cell science · 2020
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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.

Daniel RichmondDepartment of Biomedical Sciences, College of Medicine, Florida State University, Tallahassee, FL 32306, USA.
Raed Rizkallah
Fengshan Liang
Myra M Hurt
Yanchang Wang

Funding

Investigate the Molecular Basis that Controls the Timing of Spindle ElongationR15GM097326 · NIGMS · FLORIDA STATE UNIVERSITY · PI WANG, YANCHANG · 2011 to 2011
$281k
NIGMS NIH HHS R15 GM097326NIGMS NIH HHS R15GM097326-01
6 · The paper itself

Abstract

In all eukaryotic cells, DNA is packaged into multiple chromosomes that are linked to microtubules through a large protein complex called a kinetochore. Previous data show that the kinetochores are clustered together during most of the cell cycle, but the mechanism and the biological significance of kinetochore clustering are unknown. As a kinetochore protein in budding yeast, the role of Slk19 in the stability of the anaphase spindle has been well studied, but its function in chromosome segregation has remained elusive. Here we show that Slk19 is required for kinetochore clustering when yeast cells are treated with the microtubule-depolymerizing agent nocodazole. We further find that slk19Δ mutant cells exhibit delayed kinetochore capture and chromosome bipolar attachment after the disruption of the kinetochore-microtubule interaction by nocodazole, which is likely attributed to defective kinetochore clustering. In addition, we show that Slk19 interacts with itself, suggesting that the dimerization of Slk19 may mediate the interaction between kinetochores for clustering. Therefore Slk19 likely acts as kinetochore glue that clusters kinetochores to facilitate efficient and faithful chromosome segregation.

Indexed as

AnaphaseChromosomesChromosome SegregationDNAKinetochoresMicrotubule-Associated ProteinsMicrotubulesMitosisMutationNocodazoleSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSpindle ApparatusDNAMicrotubule-Associated ProteinsNocodazoleSaccharomyces cerevisiae ProteinsSlk19 protein, S cerevisiae

Identifiers

PMID23283988
PMCPMC3583661

What OpenQuestion holds

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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.