Evidence map›Paper›PMID 23955301›Full record

ArticleNature cell biology2013

Kinetochore kinesin CENP-E is a processive bi-directional tracker of dynamic microtubule tips.

Nikita Gudimchuk, Benjamin Vitre, Yumi Kim, Anatoly Kiyatkin, Don W Cleveland, Fazly I Ataullakhanov, Ekaterina L Grishchuk

Abstract read
In one paragraph

Article in Nature cell biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing 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

85 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Mechanism and regulation of kinesin motors.Nature reviews. Molecular cell biology · 2025
    Review
  8. Article
  9. Molecular evolution of the mammalian kinetochore complex.bioRxiv : the preprint server for biology · 2024
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

25 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Nikita Gudimchuk *Physiology Department, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Benjamin Vitre *Ludwig Institute for Cancer Research and Department of Cellular and Molecular Medicine, Univ. of California, San Diego, La Jolla, CA, United States.
Yumi KimLudwig Institute for Cancer Research and Department of Cellular and Molecular Medicine, Univ. of California, San Diego, La Jolla, CA, United States.
Anatoly KiyatkinPhysiology Department, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Don W ClevelandLudwig Institute for Cancer Research and Department of Cellular and Molecular Medicine, Univ. of California, San Diego, La Jolla, CA, United States.
Fazly I AtaullakhanovCenter for Theoretical Problems of Physicochemical Pharmacology, Russian Academy of Sciences, Moscow, Russian Federation.
Ekaterina L GrishchukPhysiology Department, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.

Funding

U of Calif, San Diego Neuroscience Microscopy ImagingP30NS047101 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GLEESON, JOSEPH G, ZHENG, BINHAI · 2003 to 2022
$9.0M
MICROTUBULE REGULATIONR01GM029513 · NIGMS · LUDWIG INSTITUTE FOR CANCER RES LTD · PI CLEVELAND, DON W · 1985 to 2016
$8.2M
MICROTUBULE POLYMERIZATION AND DYNAMICS IN VIVOR01GM033787 · NIGMS · UNIVERSITY OF COLORADO AT BOULDER · PI MCINTOSH, JOHN RICHARD · 1985 to 2017
$6.5M
Coupling kinetochore microtubule dynamics to chromosome motionR01GM098389 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI GRISHCHUK, EKATERINA L · 2012 to 2020
$3.1M
NIGMS NIH HHS GM033787NIGMS NIH HHS R01 GM029513NIGMS NIH HHS R01 GM033787NIGMS NIH HHS R01 GM098389NIGMS NIH HHS R01-GM098389NIGMS NIH HHS R01-GM29513NINDS NIH HHS P30 NS047101
6 · The paper itself

Abstract

During vertebrate mitosis, the centromere-associated kinesin CENP-E (centromere protein E) transports misaligned chromosomes to the plus ends of spindle microtubules. Subsequently, the kinetochores that form at the centromeres establish stable associations with microtubule ends, which assemble and disassemble dynamically. Here we provide evidence that after chromosomes have congressed and bi-oriented, the CENP-E motor continues to play an active role at kinetochores, enhancing their links with dynamic microtubule ends. Using a combination of single-molecule approaches and laser trapping in vitro, we demonstrate that once reaching microtubule ends, CENP-E converts from a lateral transporter into a microtubule tip-tracker that maintains association with both assembling and disassembling microtubule tips. Computational modelling of this behaviour supports our proposal that CENP-E tip-tracks bi-directionally through a tethered motor mechanism, which relies on both the motor and tail domains of CENP-E. Our results provide a molecular framework for the contribution of CENP-E to the stability of attachments between kinetochores and dynamic microtubule ends.

Indexed as

Cell Cycle ProteinsCell MovementChromosomal Proteins, Non-HistoneChromosome SegregationGene ExpressionHeLa CellsHumansKinetochoresMechanotransduction, CellularMicrotubulesMitosisProtein TransportSpindle ApparatusCell Cycle Proteinscentromere protein EChromosomal Proteins, Non-Histone

Identifiers

PMID23955301
PMCPMC3919686

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Registered trials

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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.