Evidence map›Paper›PMID 37658044›Full record

ArticleNature communications2023

CENP-E activation by Aurora A and B controls kinetochore fibrous corona disassembly.

Susana Eibes, Girish Rajendraprasad, Claudia Guasch-Boldu, Mirela Kubat, Yulia Steblyanko, Marin Barisic

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. Structure and function of the outer kinetochore.Nature reviews. Molecular cell biology · 2026
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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

6 authors at 1 institution in 1 country.

Susana EibesCell Division and Cytoskeleton, Danish Cancer Institute, Copenhagen, Denmark.ORCID http://orcid.org/0009-0006-3764-2113
Girish RajendraprasadCell Division and Cytoskeleton, Danish Cancer Institute, Copenhagen, Denmark.ORCID http://orcid.org/0000-0003-2521-3005
Claudia Guasch-BolduCell Division and Cytoskeleton, Danish Cancer Institute, Copenhagen, Denmark.ORCID http://orcid.org/0000-0001-5009-9924
Mirela KubatCell Division and Cytoskeleton, Danish Cancer Institute, Copenhagen, Denmark.
Yulia SteblyankoCell Division and Cytoskeleton, Danish Cancer Institute, Copenhagen, Denmark.
Marin BarisicCell Division and Cytoskeleton, Danish Cancer Institute, Copenhagen, Denmark. barisic@cancer.dk.ORCID http://orcid.org/0000-0001-7587-3867
University of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accurate chromosome segregation in mitosis depends on multiprotein structures called kinetochores that are built on the centromeric region of sister chromatids and serve to capture mitotic spindle microtubules. In early mitosis, unattached kinetochores expand a crescent-shaped structure called fibrous corona whose function is to facilitate initial kinetochore-microtubule attachments and chromosome transport by microtubules. Subsequently, the fibrous corona must be timely disassembled to prevent segregation errors. Although recent studies provided new insights on the molecular content and mechanism of fibrous corona assembly, it remains unknown what triggers the disassembly of the outermost and dynamic layer of the kinetochore. Here, we show that Aurora A and B kinases phosphorylate CENP-E to release it from an autoinhibited state. At kinetochores, Aurora B phosphorylates CENP-E to prevent its premature removal together with other corona proteins by dynein. At the spindle poles, Aurora A phosphorylates CENP-E to promote chromosome congression and prevent accumulation of corona proteins at the centrosomes, allowing for their intracellular redistribution. Thus, we propose the Aurora A/B-CENP-E axis as a critical element of the long-sought-for mechanism of fibrous corona disassembly that is essential for accurate chromosome segregation.

Indexed as

CentromereKinetochoresAurora Kinase AAurora Kinase BCell Nucleus DivisionCentrosomeChromosomal Proteins, Non-HistoneHumansSpindle ApparatusAURKA protein, humanAURKB protein, humanAurora Kinase AAurora Kinase Bcentromere protein EChromosomal Proteins, Non-Histone

Identifiers

PMID37658044
PMCPMC10474297
OpenAlexW4386371304

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.