Evidence map›Paper›PMID 29187526›Full record

ArticleThe Journal of cell biology2018

Aurora A kinase phosphorylates Hec1 to regulate metaphase kinetochore-microtubule dynamics.

Keith F DeLuca, Amanda Meppelink, Amanda J Broad, Jeanne E Mick, Olve B Peersen, Sibel Pektas, Susanne M A Lens, Jennifer G DeLuca

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

70 citing papers in PubMed, 107 citations in OpenAlex.

  1. Structure and function of the outer kinetochore.Nature reviews. Molecular cell biology · 2026
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  13. Assessment of Chromosome Oscillations in Mammalian Cells by Live Cell Imaging.Methods in molecular biology (Clifton, N.J.) · 2025
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  17. Genetic interaction mapping of Aurora protein kinases in mouse oocytes.Frontiers in cell and developmental biology · 2024
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10 more citing papers are in PubMed but not listed here.

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 2 countries.

Keith F DeLucaDepartment of Biochemistry and Molecular Biology, Colorado State University, Fort Collins, CO.
Amanda MeppelinkOncode Institute, Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, Netherlands.ORCID 0000-0003-1061-7373
Amanda J BroadDepartment of Biochemistry and Molecular Biology, Colorado State University, Fort Collins, CO.
Jeanne E MickDepartment of Biochemistry and Molecular Biology, Colorado State University, Fort Collins, CO.
Olve B PeersenDepartment of Biochemistry and Molecular Biology, Colorado State University, Fort Collins, CO.
Sibel PektasOncode Institute, Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, Netherlands.
Susanne M A LensOncode Institute, Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, Netherlands s.m.a.lens@umcutrecht.nl.ORCID 0000-0003-2199-7594
Jennifer G DeLucaDepartment of Biochemistry and Molecular Biology, Colorado State University, Fort Collins, CO jdeluca@colostate.edu.ORCID 0000-0002-3598-1721
Colorado State University · USUniversity Medical Center Utrecht · NL

Funding

Kinetochore Function in Vertebrate CellsR01GM088371 · NIGMS · COLORADO STATE UNIVERSITY · PI DELUCA, JENNIFER G · 2010 to 2018
$3.1M
NIGMS NIH HHS R01 GM088371
6 · The paper itself

Abstract

Precise regulation of kinetochore-microtubule attachments is essential for successful chromosome segregation. Central to this regulation is Aurora B kinase, which phosphorylates kinetochore substrates to promote microtubule turnover. A critical target of Aurora B is the N-terminal "tail" domain of Hec1, which is a component of the NDC80 complex, a force-transducing link between kinetochores and microtubules. Although Aurora B is regarded as the "master regulator" of kinetochore-microtubule attachment, other mitotic kinases likely contribute to Hec1 phosphorylation. In this study, we demonstrate that Aurora A kinase regulates kinetochore-microtubule dynamics of metaphase chromosomes, and we identify Hec1 S69, a previously uncharacterized phosphorylation target site in the Hec1 tail, as a critical Aurora A substrate for this regulation. Additionally, we demonstrate that Aurora A kinase associates with inner centromere protein (INCENP) during mitosis and that INCENP is competent to drive accumulation of the kinase to the centromere region of mitotic chromosomes. These findings reveal that both Aurora A and B contribute to kinetochore-microtubule attachment dynamics, and they uncover an unexpected role for Aurora A in late mitosis.

Indexed as

AnimalsAurora Kinase AAurora Kinase BCell Line, TumorCentromereChromosomal Proteins, Non-HistoneChromosome SegregationCytoskeletal ProteinsHeLa CellsHumansKinetochoresMetaphaseMicrotubulesNuclear ProteinsPhosphorylationPotoroidaeAURKA protein, humanAURKB protein, humanAurora Kinase AAurora Kinase BChromosomal Proteins, Non-HistoneCytoskeletal ProteinsINCENP protein, humanNDC80 protein, humanNuclear Proteins

Identifiers

PMID29187526
PMCPMC5748988
OpenAlexW2770198328

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.