Evidence map›Paper›PMID 27325791›Full record

ArticleThe Journal of cell biology2016

A noncatalytic function of the topoisomerase II CTD in Aurora B recruitment to inner centromeres during mitosis.

Heather Edgerton, Marnie Johansson, Daniel Keifenheim, Soumya Mukherjee, Jeremy M Chacón, Jeff Bachant, Melissa K Gardner, Duncan J Clarke

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.6field-weighted citation impact, top 8% 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

34 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
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  4. Histone H3 tail modifications required for meiosis inbioRxiv : the preprint server for biology · 2024
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  13. Article
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  15. Article
  16. SUMO: A Swiss Army Knife for Eukaryotic Topoisomerases.Frontiers in molecular biosciences · 2022
    Review
  17. Review
  18. Review
  19. Review
  20. Article
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

8 authors at 2 institutions in 1 country.

Heather EdgertonDepartment of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, MN 55455.ORCID 0000-0003-3578-6704
Marnie JohanssonDepartment of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, MN 55455.
Daniel KeifenheimDepartment of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, MN 55455.
Soumya MukherjeeDepartment of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, MN 55455.ORCID 0000-0003-3040-4658
Jeremy M ChacónDepartment of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, MN 55455.
Jeff BachantDepartment of Cell Biology and Neuroscience, University of California, Riverside, Riverside, CA 92521.
Melissa K GardnerDepartment of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, MN 55455.
Duncan J ClarkeDepartment of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, MN 55455 clark140@umn.edu.ORCID 0000-0002-7795-3294
University of Minnesota · USUniversity of California, Riverside · US

Funding

Quantitative Analysis and Modeling of Microtubule Structure and RegulationR01GM103833 · NIGMS · UNIVERSITY OF MINNESOTA · PI GARDNER, MELISSA · 2013 to 2017
$1.4M
Regulation of kinetochore function by Topoisomerase IIR01GM112793 · NIGMS · UNIVERSITY OF KANSAS LAWRENCE · PI AZUMA, YOSHIAKI, CLARKE, DUNCAN J. · 2015 to 2018
$1.2M
NIGMS NIH HHS R01 GM103833NIGMS NIH HHS R01 GM112793
6 · The paper itself

Abstract

Faithful chromosome segregation depends on the precise timing of chromatid separation, which is enforced by checkpoint signals generated at kinetochores. Here, we provide evidence that the C-terminal domain (CTD) of DNA topoisomerase IIα (Topo II) provides a novel function at inner centromeres of kinetochores in mitosis. We find that the yeast CTD is required for recruitment of the tension checkpoint kinase Ipl1/Aurora B to inner centromeres in metaphase but is not required in interphase. Conserved CTD SUMOylation sites are required for Ipl1 recruitment. This inner-centromere CTD function is distinct from the catalytic activity of Topo II. Genetic and biochemical evidence suggests that Topo II recruits Ipl1 via the Haspin-histone H3 threonine 3 phosphorylation pathway. Finally, Topo II and Sgo1 are equally important for Ipl1 recruitment to inner centromeres. This indicates H3 T3-Phos/H2A T120-Phos is a universal epigenetic signature that defines the eukaryotic inner centromere and provides the binding site for Ipl1/Aurora B.

Indexed as

Antigens, NeoplasmAurora Kinase BCell Cycle ProteinsCentromereChromatidsChromosome SegregationDNA-Binding ProteinsDNA Topoisomerases, Type IIFungal ProteinsHistonesKinetochoresMetaphasePhosphorylationProtein Serine-Threonine KinasesSumoylationYeastsAntigens, NeoplasmAurora Kinase BCell Cycle ProteinsDNA-Binding ProteinsDNA Topoisomerases, Type IIFungal ProteinsHistonesProtein Serine-Threonine Kinases

Identifiers

PMID27325791
PMCPMC4915189
OpenAlexW2463504972

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.