Evidence map›Paper›PMID 31757788›Full record

ArticleThe Journal of cell biology2020

CLASP2 binding to curved microtubule tips promotes flux and stabilizes kinetochore attachments.

Hugo Girão, Naoyuki Okada, Tony A Rodrigues, Alexandra O Silva, Ana C Figueiredo, Zaira Garcia, Tatiana Moutinho-Santos, Ikuko Hayashi, Jorge E Azevedo, Sandra Macedo-Ribeiro and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

18 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  5. Analysis ofAnimals : an open access journal from MDPI · 2023
    Article
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  7. Mechanisms underlying spindle assembly and robustness.Nature reviews. Molecular cell biology · 2023
    Review
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  14. 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
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  16. 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

11 authors at 2 institutions in 2 countries.

Hugo GirãoInstituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.
Naoyuki OkadaInstituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.
Tony A RodriguesInstituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.
Alexandra O SilvaInstituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.
Ana C FigueiredoInstituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.
Zaira GarciaInstituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.
Tatiana Moutinho-SantosInstituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.
Ikuko HayashiInternational Graduate School of Arts and Sciences, Yokohama City University, Yokohama, Japan.
Jorge E AzevedoInstituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.
Sandra Macedo-RibeiroInstituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.
Helder MaiatoInstituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.
Universidade do Porto · PTYokohama City University · JP

Funding

European Research Council 681443
6 · The paper itself

Abstract

CLASPs are conserved microtubule plus-end-tracking proteins that suppress microtubule catastrophes and independently localize to kinetochores during mitosis. Thus, CLASPs are ideally positioned to regulate kinetochore-microtubule dynamics required for chromosome segregation fidelity, but the underlying mechanism remains unknown. Here, we found that human CLASP2 exists predominantly as a monomer in solution, but it can self-associate through its C-terminal kinetochore-binding domain. Kinetochore localization was independent of self-association, and driving monomeric CLASP2 to kinetochores fully rescued normal kinetochore-microtubule dynamics, while partially sustaining mitosis. CLASP2 kinetochore localization, recognition of growing microtubule plus-ends through EB-protein interaction, and the ability to associate with curved microtubule protofilaments through TOG2 and TOG3 domains independently sustained normal spindle length, timely spindle assembly checkpoint satisfaction, chromosome congression, and faithful segregation. Measurements of kinetochore-microtubule half-life and poleward flux revealed that CLASP2 regulates kinetochore-microtubule dynamics by integrating distinctive microtubule-binding properties at the kinetochore-microtubule interface. We propose that kinetochore CLASP2 suppresses microtubule depolymerization and detachment by binding to curved protofilaments at microtubule plus-ends.

Indexed as

Chromosome SegregationHeLa CellsHumansKinetochoresMicrotubule-Associated ProteinsMicrotubulesMitosisM Phase Cell Cycle CheckpointsProtein BindingProtein DomainsSpindle ApparatusCLASP2 protein, humanMicrotubule-Associated Proteins

Identifiers

PMID31757788
PMCPMC7041679
OpenAlexW2991245854

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.