Evidence map›Paper›PMID 32348198›Full record

ArticleMolecular biology of the cell2020

Centrosome-nuclear axis repositioning drives the assembly of a bipolar spindle scaffold to ensure mitotic fidelity.

Vanessa Nunes, Margarida Dantas, Domingos Castro, Elisa Vitiello, Irène Wang, Nicolas Carpi, Martial Balland, Matthieu Piel, Paulo Aguiar, Helder Maiato and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular biology of the cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

21 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. The kinetochore corona orchestrates chromosome congression through transient microtubule interactions.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Positioning centrioles and centrosomes.The Journal of cell biology · 2024
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Moonlighting at the Poles: Non-Canonical Functions of Centrosomes.Frontiers in cell and developmental biology · 2022
    Review
  18. Review
  19. Nucleus-Cytoskeleton Crosstalk During Mitotic Entry.Frontiers in cell and developmental biology · 2021
    Review
  20. Review
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 5 institutions in 2 countries.

Vanessa NunesInstituto de Investigação e Inovação em Saúde (i3S), 4200-135 Porto, Portugal.
Margarida DantasInstituto de Investigação e Inovação em Saúde (i3S), 4200-135 Porto, Portugal.
Domingos CastroInstituto de Investigação e Inovação em Saúde (i3S), 4200-135 Porto, Portugal.
Elisa VitielloLaboratoire Interdisciplinaire de Physique, Université Joseph Fourier (Grenoble 1) 38058, France.
Irène WangLaboratoire Interdisciplinaire de Physique, Université Joseph Fourier (Grenoble 1) 38058, France.
Nicolas CarpiInstitut Curie, PSL Research University, CNRS, UMR 144, F-75005 Paris, France.
Martial BallandLaboratoire Interdisciplinaire de Physique, Université Joseph Fourier (Grenoble 1) 38058, France.
Matthieu PielInstitut Curie, PSL Research University, CNRS, UMR 144, F-75005 Paris, France.
Paulo AguiarInstituto de Investigação e Inovação em Saúde (i3S), 4200-135 Porto, Portugal.
Helder MaiatoInstituto de Investigação e Inovação em Saúde (i3S), 4200-135 Porto, Portugal.
Jorge G FerreiraInstituto de Investigação e Inovação em Saúde (i3S), 4200-135 Porto, Portugal.
Université Joseph Fourier · FRCentre National de la Recherche Scientifique · FRi3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto · PTNational Institute of Engineering, Technology and Innovation · PTUniversidade do Porto · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During the initial stages of cell division, the cytoskeleton is extensively reorganized so that a bipolar mitotic spindle can be correctly assembled. This process occurs through the action of molecular motors, cytoskeletal networks, and the nucleus. How the combined activity of these different components is spatiotemporally regulated to ensure efficient spindle assembly remains unclear. To investigate how cell shape, cytoskeletal organization, and molecular motors cross-talk to regulate initial spindle assembly, we use a combination of micropatterning with high-resolution imaging and 3D cellular reconstruction. We show that during prophase, centrosomes and nucleus reorient so that centrosomes are positioned on the shortest nuclear axis at nuclear envelope (NE) breakdown. We also find that this orientation depends on a combination of centrosome movement controlled by Arp2/3-mediated regulation of microtubule dynamics and Dynein-generated forces on the NE that regulate nuclear reorientation. Finally, we observe this centrosome configuration favors the establishment of an initial bipolar spindle scaffold, facilitating chromosome capture and accurate segregation, without compromising division plane orientation.

Indexed as

MitosisActin-Related Protein 2-3 ComplexCell AdhesionCell ShapeCentrosomeDyneinsHEK293 CellsHeLa CellsHumansMovementNuclear EnvelopeProphaseRotationSpindle ApparatusActin-Related Protein 2-3 ComplexDyneins

Identifiers

PMID32348198
PMCPMC7521851
OpenAlexW3020808162

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.