Evidence map›Paper›PMID 11950924›Full record

ArticleMolecular biology of the cell2002

Probing the dynamics and functions of aurora B kinase in living cells during mitosis and cytokinesis.

Maki Murata-Hori, Masaaki Tatsuka, Yu-Li Wang

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
5.4field-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

80 citing papers in PubMed, 197 citations in OpenAlex.

  1. Article
  2. Proangiogenic effect and molecular mechanism of a new cytosporin derivative from the marine fungus Eutypella sp. D-1.Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2026
    Article
  3. Review
  4. Article
  5. Double-checking chromosome segregation.The Journal of cell biology · 2023
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. The Cockayne syndrome group A and B proteins are part of a ubiquitin-proteasome degradation complex regulating cell division.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  11. Article
  12. Article
  13. Abnormal nuclear aggregation and myotube degeneration in myotonic dystrophy type 1.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2019
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

20 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

3 authors at 2 institutions in 2 countries.

Maki Murata-HoriDepartment of Physiology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Masaaki Tatsuka
Yu-Li Wang
University of Massachusetts Chan Medical School · USHiroshima University · JP

Funding

DYNAMICS OF ACTIN IN NORMAL AND TRANSFORMED CELLSR37GM032476 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI WANG, YU-LI · 1998 to 2007
$3.4M
DYNAMICS OF ACTIN STRUCTURES DURING CELL TRANSFORMATIONR01GM032476 · NIGMS · WORCESTER FOUNDATION FOR BIOMEDICAL RES · PI WANG, YU-LI · 1986 to 2011
$2.0M
NIGMS NIH HHS GM-32476NIGMS NIH HHS R01 GM032476NIGMS NIH HHS R37 GM032476
6 · The paper itself

Abstract

Aurora B is a protein kinase and a chromosomal passenger protein that undergoes dynamic redistribution during mitosis. We have probed the mechanism that regulates its localization with cells expressing green fluorescent protein (GFP)-tagged wild-type or mutant aurora B. Aurora B was found at centromeres at prophase and persisted until approximately 0.5 min after anaphase onset, when it redistributed to the spindle midzone and became concentrated at the equator along midzone microtubules. Depolymerization of microtubules inhibited the dissociation of aurora B from centromeres at early anaphase and caused the dispersion of aurora B from the spindle midzone at late anaphase; however, centromeric association during prometaphase was unaffected. Inhibition of CDK1 deactivation similarly caused aurora B to remain associated with centromeres during anaphase. In contrast, inhibition of the kinase activity of aurora B appeared to have no effect on its interactions with centromeres or initial relocation onto midzone microtubules. Instead, kinase-inactive aurora B caused abnormal mitosis and deactivation of the spindle checkpoint. In addition, midzone microtubule bundles became destabilized and aurora B dispersed from the equator. Our results suggest that microtubules, CDK1, and the kinase activity each play a distinct role in the dynamics and functions of aurora B in dividing cells.

Indexed as

Cell DivisionMitosisAnimalsAurora Kinase BAurora KinasesCells, CulturedCyclin BGreen Fluorescent ProteinsKidneyLuminescent ProteinsMicroscopy, FluorescenceMicrotubulesModels, BiologicalPlasmidsProtein Serine-Threonine KinasesRatsAurkb protein, ratAurora Kinase BAurora KinasesCyclin BGreen Fluorescent ProteinsLuminescent ProteinsProtein Serine-Threonine KinasesRecombinant Fusion ProteinsRhodaminesTubulin

Identifiers

PMID11950924
PMCPMC102254
OpenAlexW2102770794

What OpenQuestion holds

Textmetadata
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.