Evidence map›Paper›PMID 22099307›Full record

ArticleMolecular cell2011

Aurora-B mediated ATM serine 1403 phosphorylation is required for mitotic ATM activation and the spindle checkpoint.

Chunying Yang, Xi Tang, Xiaojing Guo, Yohei Niikura, Katsumi Kitagawa, Kemi Cui, Stephen T C Wong, Li Fu, Bo Xu

Abstract read
In one paragraph

Article in Molecular cell, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
5.1field-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

77 citing papers in PubMed, 105 citations in OpenAlex.

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17 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

9 authors at 5 institutions in 2 countries.

Chunying YangDepartment of Radiation Oncology, The Methodist Hospital Research Institute, Weill Cornell Medical College, Houston, TX 77030, USA.
Xi Tang
Xiaojing Guo
Yohei Niikura
Katsumi Kitagawa
Kemi Cui
Stephen T C Wong
Li Fu
Bo Xu
Cornell University · USHouston Methodist · USNationwide Children's Hospital · USSouthern Research Institute · USTianjin Medical University Cancer Institute and Hospital · CN

Funding

The Core of the Computational BiologyU54CA149196 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI WONG, STEPHEN TC · 2010 to 2015
$10.6M
Kinetochore Function and Cell Cycle Progression RevisionR01GM068418 · NIGMS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI KITAGAWA, KATSUMI · 2003 to 2012
$2.5M
Mechanisms of Mitotic Activation of the ATM kinaseR01CA133093 · NCI · SOUTHERN RESEARCH INSTITUTE · PI XU, BO · 2009 to 2013
$1.4M
High-content Image Analysis and Modeling for RANigenome-wide ScreeningR01CA121225 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI WONG, STEPHEN TC · 2008 to 2011
$1.2M
A Novel Pathway Involving ATM, PP1 and I-2R01ES016354 · NIEHS · SOUTHERN RESEARCH INSTITUTE · PI MITRA, SANKAR · 2009 to 2012
$1.1M
Defining lineage-specific determinants of K-Ras "addiction" in human cancersR00CA149169 · NCI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI SINGH, ANURAG · 2012 to 2014
$710k
Defining lineage-specific determinants of K-Ras "addiction" in human cancersK99CA149169 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI SINGH, ANURAG · 2010 to 2011
$268k
An HTS Assay for Inhibitors of NBS1-ATM InteractionsR21NS061748 · NINDS · SOUTHERN RESEARCH INSTITUTE · PI XU, BO · 2007 to 2007
$211k
NCI NIH HHS K99 CA149169NCI NIH HHS R00 CA149169NCI NIH HHS R01 CA121225NCI NIH HHS R01CA121225NCI NIH HHS R01 CA133093NCI NIH HHS R01CA133093NCI NIH HHS U54CA149169NCI NIH HHS U54 CA149196NIEHS NIH HHS R01 ES016354NIEHS NIH HHS R01ES016354NIGMS NIH HHS R01 GM068418NIGMS NIH HHS R01GM68418NINDS NIH HHS R21 NS061748NINDS NIH HHS R21NS061748
6 · The paper itself

Abstract

The ATM kinase plays a critical role in the maintenance of genetic stability. ATM is activated in response to DNA damage and is essential for cell-cycle checkpoints. Here, we report that ATM is activated in mitosis in the absence of DNA damage. We demonstrate that mitotic ATM activation is dependent on the Aurora-B kinase and that Aurora-B phosphorylates ATM on serine 1403. This phosphorylation event is required for mitotic ATM activation. Further, we show that loss of ATM function results in shortened mitotic timing and a defective spindle checkpoint, and that abrogation of ATM Ser1403 phosphorylation leads to this spindle checkpoint defect. We also demonstrate that mitotically activated ATM phosphorylates Bub1, a critical kinetochore protein, on Ser314. ATM-mediated Bub1 Ser314 phosphorylation is required for Bub1 activity and is essential for the activation of the spindle checkpoint. Collectively, our data highlight mechanisms of a critical function of ATM in mitosis.

Indexed as

Genome, HumanGenomic InstabilityAtaxia Telangiectasia Mutated ProteinsAurora Kinase BAurora KinasesCell Cycle ProteinsDNA-Binding ProteinsEnzyme ActivationFlow CytometryGene SilencingHEK293 CellsHeLa CellsHumansKinetochoresMitosisPhosphorylationAtaxia Telangiectasia Mutated ProteinsATM protein, humanAURKB protein, humanAurora Kinase BAurora KinasesBUB1 protein, humanBub1 spindle checkpoint proteinCell Cycle ProteinsDNA-Binding ProteinsProtein Serine-Threonine KinasesRNA, Small InterferingSerineTumor Suppressor Proteins

Identifiers

PMID22099307
PMCPMC3228519
OpenAlexW1968385175

What OpenQuestion holds

Textmetadata
LicenceTDM
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.