Evidence map›Paper›PMID 23045552›Full record

ArticleThe Journal of cell biology2012

Cdk1 and Plk1 mediate a CLASP2 phospho-switch that stabilizes kinetochore-microtubule attachments.

Ana R R Maia, Zaira Garcia, Lilian Kabeche, Marin Barisic, Stefano Maffini, Sandra Macedo-Ribeiro, Iain M Cheeseman, Duane A Compton, Irina Kaverina, Helder Maiato

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

67 citing papers in PubMed, 90 citations in OpenAlex.

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  12. Cortical microtubules oppose actomyosin-driven membrane ingression duringbioRxiv : the preprint server for biology · 2023
    Article
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  19. SOGA1 and SOGA2/MTCL1 are CLASP-interacting proteins required for faithful chromosome segregation in human cells.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2021
    Article
  20. Review

7 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

10 authors at 4 institutions in 2 countries.

Ana R R MaiaInstituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.
Zaira Garcia
Lilian Kabeche
Marin Barisic
Stefano Maffini
Sandra Macedo-Ribeiro
Iain M Cheeseman
Duane A Compton
Irina Kaverina
Helder Maiato
Universidade do Porto · PTUSC Norris Comprehensive Cancer Center · USMassachusetts Institute of Technology · USVanderbilt University Medical Center · US

Funding

Organization of the Mammalian Mitotic SpindleR37GM051542 · NIGMS · DARTMOUTH COLLEGE · PI COMPTON, DUANE A. · 2013 to 2022
$6.7M
Organization of the Mammilian Mitotic SpindleR01GM051542 · NIGMS · DARTMOUTH COLLEGE · PI COMPTON, DUANE A. · 1996 to 2012
$4.6M
Molecular Analysis of the Kinetochore-Microtubule InterfaceR01GM088313 · NIGMS · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI CHEESEMAN, IAIN MCPHERSON · 2009 to 2017
$3.6M
Spatial Regulation of Cytoskeletal AsymmetryR01GM078373 · NIGMS · VANDERBILT UNIVERSITY · PI KAVERINA, IRINA · 2008 to 2017
$3.2M
NIGMS NIH HHS 5R01-GM078373NIGMS NIH HHS GM088313NIGMS NIH HHS GM51542NIGMS NIH HHS R01 GM051542NIGMS NIH HHS R01 GM078373NIGMS NIH HHS R01 GM088313NIGMS NIH HHS R37 GM051542
6 · The paper itself

Abstract

Accurate chromosome segregation during mitosis relies on a dynamic kinetochore (KT)-microtubule (MT) interface that switches from a labile to a stable condition in response to correct MT attachments. This transition is essential to satisfy the spindle-assembly checkpoint (SAC) and couple MT-generated force with chromosome movements, but the underlying regulatory mechanism remains unclear. In this study, we show that during mitosis the MT- and KT-associated protein CLASP2 is progressively and distinctively phosphorylated by Cdk1 and Plk1 kinases, concomitant with the establishment of KT-MT attachments. CLASP2 S1234 was phosphorylated by Cdk1, which primed CLASP2 for association with Plk1. Plk1 recruitment to KTs was enhanced by CLASP2 phosphorylation on S1234. This was specifically required to stabilize KT-MT attachments important for chromosome alignment and to coordinate KT and non-KT MT dynamics necessary to maintain spindle bipolarity. CLASP2 C-terminal phosphorylation by Plk1 was also required for chromosome alignment and timely satisfaction of the SAC. We propose that Cdk1 and Plk1 mediate a fine CLASP2 "phospho-switch" that temporally regulates KT-MT attachment stability.

Indexed as

CDC2 Protein KinaseCell Cycle ProteinsCell Line, TumorChromosome SegregationHeLa CellsHumansKinetochoresMicrotubule-Associated ProteinsMicrotubulesMitosisM Phase Cell Cycle CheckpointsPhosphorylationPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsSpindle ApparatusCDC2 Protein KinaseCell Cycle ProteinsCLASP2 protein, humanMicrotubule-Associated ProteinsPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene Proteins

Identifiers

PMID23045552
PMCPMC3471233
OpenAlexW2170492817

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.