Evidence map›Paper›PMID 19494039›Full record

ArticleMolecular biology of the cell2009

Molecular distinctions between Aurora A and B: a single residue change transforms Aurora A into correctly localized and functional Aurora B.

Fabienne Hans, Dimitrios A Skoufias, Stefan Dimitrov, Robert L Margolis

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

38 citing papers in PubMed, 64 citations in OpenAlex.

  1. Review
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  7. Aurora B kinase: a potential drug target for cancer therapy.Journal of cancer research and clinical oncology · 2021
    Review
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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

4 authors at 2 institutions in 2 countries.

Fabienne HansInstitut National de la Santé et de la Recherche Médicale, Université Joseph Fourier-Grenoble 1, Grenoble, France.
Dimitrios A Skoufias
Stefan Dimitrov
Robert L Margolis
Centre National de la Recherche Scientifique · FRInserm · FR

Funding

Induction of Cell Cleavage by the Mitotic SpindleR01GM068107 · NIGMS · SIDNEY KIMMEL CANCER CENTER · PI MARGOLIS, ROBERT LEWIS · 2005 to 2009
$1.8M
NIGMS NIH HHS R01 GM-068107NIGMS NIH HHS R01 GM068107
6 · The paper itself

Abstract

Aurora A and Aurora B, paralogue mitotic kinases, share highly similar primary sequence. Both are important to mitotic progression, but their localizations and functions are distinct. We have combined shRNA suppression with overexpression of Aurora mutants to address the cause of the distinction between Aurora A and Aurora B. Aurora A residue glycine 198 (G198), mutated to asparagine to mimic the aligned asparagine 142 (N142) of Aurora B, causes Aurora A to bind the Aurora B binding partner INCENP but not the Aurora A binding partner TPX2. The mutant Aurora A rescues Aurora B mitotic function. We conclude that binding to INCENP is alone critical to the distinct function of Aurora B. Although G198 of Aurora A is required for TPX2 binding, N142G Aurora B retains INCENP binding and Aurora B function. Thus, although a single residue change transforms Aurora A, the reciprocal mutation of Aurora B does not create Aurora A function. An Aurora A-Delta120 N-terminal truncation construct reinforces Aurora A similarity to Aurora B, because it does not associate with centrosomes but instead associates with kinetochores.

Indexed as

Amino Acid SubstitutionAmino Acid SequenceAnimalsAurora Kinase BAurora KinasesBinding SitesCell Cycle ProteinsChromosomal Proteins, Non-HistoneHCT116 CellsHeLa CellsHistonesHumansImmunoprecipitationMicrotubule-Associated ProteinsMitosisModels, MolecularAURKB protein, humanAurora Kinase BAurora KinasesCell Cycle ProteinsChromosomal Proteins, Non-HistoneHistonesINCENP protein, humanMicrotubule-Associated ProteinsNuclear ProteinsProtein Serine-Threonine KinasesTPX2 protein, humanXenopus Proteins

Identifiers

PMID19494039
PMCPMC2719567
OpenAlexW2040633485

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.