Evidence map›Paper›PMID 32050025›Full record

ArticleThe Journal of cell biology2020

Regulated changes in material properties underlie centrosome disassembly during mitotic exit.

Matthäus Mittasch, Vanna M Tran, Manolo U Rios, Anatol W Fritsch, Stephen J Enos, Beatriz Ferreira Gomes, Alec Bond, Moritz Kreysing, Jeffrey B Woodruff

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 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.9field-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

34 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
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  7. Biomolecular condensates-Prerequisites for anhydrobiosis?Protein science : a publication of the Protein Society · 2025
    Review
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  15. Native molecular architectures of centrosomes inbioRxiv : the preprint server for biology · 2024
    Article
  16. Article
  17. Multiscale biophysical analysis of nucleolus disassembly during mitosis.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  18. Article
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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

9 authors at 2 institutions in 2 countries.

Matthäus MittaschMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Vanna M TranDepartments of Cell Biology and Biophysics, University of Texas Southwestern Medical Center, Dallas, TX.
Manolo U RiosDepartments of Cell Biology and Biophysics, University of Texas Southwestern Medical Center, Dallas, TX.
Anatol W FritschMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Stephen J EnosMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Beatriz Ferreira GomesMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Alec BondDepartments of Cell Biology and Biophysics, University of Texas Southwestern Medical Center, Dallas, TX.
Moritz KreysingMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Jeffrey B WoodruffDepartments of Cell Biology and Biophysics, University of Texas Southwestern Medical Center, Dallas, TX.
Max Planck Institute of Molecular Cell Biology and Genetics · DEThe University of Texas Southwestern Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Centrosomes must resist microtubule-mediated forces for mitotic chromosome segregation. During mitotic exit, however, centrosomes are deformed and fractured by those same forces, which is a key step in centrosome disassembly. How the functional material properties of centrosomes change throughout the cell cycle, and how they are molecularly tuned, remain unknown. Here, we used optically induced flow perturbations to determine the molecular basis of centrosome strength and ductility in C. elegans embryos. We found that both properties declined sharply at anaphase onset, long before natural disassembly. This mechanical transition required PP2A phosphatase and correlated with inactivation of PLK-1 (Polo kinase) and SPD-2 (Cep192). In vitro, PLK-1 and SPD-2 directly protected centrosome scaffolds from force-induced disassembly. Our results suggest that, before anaphase, PLK-1 and SPD-2 respectively confer strength and ductility to the centrosome scaffold so that it can resist microtubule-pulling forces. In anaphase, centrosomes lose PLK-1 and SPD-2 and transition to a weak, brittle state that enables force-mediated centrosome disassembly.

Indexed as

MitosisAnimalsCaenorhabditis elegansCentrosomeLeupeptinsbenzyloxycarbonylleucyl-leucyl-leucine aldehydeLeupeptins

Identifiers

PMID32050025
PMCPMC7147112
OpenAlexW3005644365

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.