Evidence map›Paper›PMID 18443223›Full record

ArticleThe Journal of cell biology2008

CENP-E combines a slow, processive motor and a flexible coiled coil to produce an essential motile kinetochore tether.

Yumi Kim, John E Heuser, Clare M Waterman, Don W Cleveland

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

97 citing papers in PubMed, 140 citations in OpenAlex.

  1. Structure and function of the outer kinetochore.Nature reviews. Molecular cell biology · 2026
    Review
  2. Review
  3. Article
  4. Article
  5. Splicing to orchestrate cell fate.Molecular therapy. Nucleic acids · 2025
    Review
  6. Mechanism and regulation of kinesin motors.Nature reviews. Molecular cell biology · 2025
    Review
  7. Article
  8. Molecular evolution of the mammalian kinetochore complex.bioRxiv : the preprint server for biology · 2024
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

37 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

4 authors at 3 institutions in 1 country.

Yumi KimLudwig Institute for Cancer Research, University of California, San Diego, La Jolla, CA 92093, USA.
John E Heuser
Clare M Waterman
Don W Cleveland
National Heart Lung and Blood Institute · USUniversity of California, San Diego · USWashington University in St. Louis · US

Funding

MICROTUBULE REGULATIONR01GM029513 · NIGMS · LUDWIG INSTITUTE FOR CANCER RES LTD · PI CLEVELAND, DON W · 1985 to 2016
$8.2M
Microtubule Actin Interactions In Cell MotilityZIAHL005103 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI WATERMAN, CLARE MICHAL · 2009 to 2013
$2.7M
MICROTUBULE REGULATIONR37GM029513 · NIGMS · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI CLEVELAND, DON W. · 1994 to 2003
$1.8M
NIGMS NIH HHS GM29513NIGMS NIH HHS R01 GM029513NIGMS NIH HHS R37 GM029513
6 · The paper itself

Abstract

The mitotic kinesin centromere protein E (CENP-E) is an essential kinetochore component that directly contributes to the capture and stabilization of spindle microtubules by kinetochores. Although reduction in CENP-E leads to high rates of whole chromosome missegregation, neither its properties as a microtubule-dependent motor nor how it contributes to the dynamic linkage between kinetochores and microtubules is known. Using single-molecule assays, we demonstrate that CENP-E is a very slow, highly processive motor that maintains microtubule attachment for long periods. Direct visualization of full-length Xenopus laevis CENP-E reveals a highly flexible 230-nm coiled coil separating its kinetochore-binding and motor domains. We also show that full-length CENP-E is a slow plus end-directed motor whose activity is essential for metaphase chromosome alignment. We propose that the highly processive microtubule-dependent motor activity of CENP-E serves to power chromosome congression and provides a flexible, motile tether linking kinetochores to dynamic spindle microtubules.

Indexed as

Protein Structure, SecondaryAnimalsChromosomal Proteins, Non-HistoneChromosome SegregationKinetochoresMicrotubulesModels, BiologicalMolecular Motor ProteinsRecombinant Fusion ProteinsSpindle ApparatusXenopus laevisXenopus Proteinscentromere protein EChromosomal Proteins, Non-HistoneMolecular Motor ProteinsRecombinant Fusion ProteinsXenopus Proteins

Identifiers

PMID18443223
PMCPMC2364708
OpenAlexW2118612987

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.