Evidence map›Paper›PMID 29097687›Full record

ArticleNature communications2017

Genome-scale single-cell mechanical phenotyping reveals disease-related genes involved in mitotic rounding.

Yusuke Toyoda, Cedric J Cattin, Martin P Stewart, Ina Poser, Mirko Theis, Teymuras V Kurzchalia, Frank Buchholz, Anthony A Hyman, Daniel J Müller

Abstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
–field-weighted citation impact
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

38 citing papers in PubMed.

  1. Article
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  3. Article
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  7. Article
  8. The Role of the Swollen State in Cell Proliferation.The Journal of membrane biology · 2025
    Review
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  10. Review
  11. Article
  12. Article
  13. Article
  14. Cortical microtubules oppose actomyosin-driven membrane ingression duringbioRxiv : the preprint server for biology · 2023
    Article
  15. Article
  16. Article
  17. Background and roles: myosin in autoimmune diseases.Frontiers in cell and developmental biology · 2023
    Review
  18. Article
  19. Article
  20. Protein and lipid mass concentration measurement in tissues by stimulated Raman scattering microscopy.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
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.

Yusuke ToyodaMax Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, 01307, Dresden, Germany.ORCID http://orcid.org/0000-0003-0534-6898
Cedric J CattinDepartment of Biosystems Science and Engineering (D-BSSE), Eidgenössische Technische Hochschule (ETH) Zurich, Mattenstrasse 26, 4058, Basel, Switzerland.
Martin P StewartDepartment of Biosystems Science and Engineering (D-BSSE), Eidgenössische Technische Hochschule (ETH) Zurich, Mattenstrasse 26, 4058, Basel, Switzerland.ORCID http://orcid.org/0000-0003-4112-6622
Ina PoserMax Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, 01307, Dresden, Germany.
Mirko TheisUCC, Medical System biology, Medical Faculty Carl Gustav Carus, University of Technology Dresden, Am Tatzberg 47/49, 01307, Dresden, Germany.
Teymuras V KurzchaliaMax Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, 01307, Dresden, Germany.
Frank BuchholzMax Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, 01307, Dresden, Germany.
Anthony A HymanMax Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, 01307, Dresden, Germany. hyman@mpi-cbg.de.
Daniel J MüllerDepartment of Biosystems Science and Engineering (D-BSSE), Eidgenössische Technische Hochschule (ETH) Zurich, Mattenstrasse 26, 4058, Basel, Switzerland. daniel.mueller@bsse.ethz.ch.ORCID http://orcid.org/0000-0003-3075-0665

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To divide, most animal cells drastically change shape and round up against extracellular confinement. Mitotic cells facilitate this process by generating intracellular pressure, which the contractile actomyosin cortex directs into shape. Here, we introduce a genome-scale microcantilever- and RNAi-based approach to phenotype the contribution of > 1000 genes to the rounding of single mitotic cells against confinement. Our screen analyzes the rounding force, pressure and volume of mitotic cells and localizes selected proteins. We identify 49 genes relevant for mitotic rounding, a large portion of which have not previously been linked to mitosis or cell mechanics. Among these, depleting the endoplasmic reticulum-localized protein FAM134A impairs mitotic progression by affecting metaphase plate alignment and pressure generation by delocalizing cortical myosin II. Furthermore, silencing the DJ-1 gene uncovers a link between mitochondria-associated Parkinson's disease and mitotic pressure. We conclude that mechanical phenotyping is a powerful approach to study the mechanisms governing cell shape.

Indexed as

Actin CytoskeletonActomyosinAnimalsBiomechanical PhenomenaCell ShapeHeLa CellsHigh-Throughput Screening AssaysHumansMembrane ProteinsMetaphaseMiceMicroscopy, Atomic ForceMitosisMyosin Type IIParkinson DiseasePhenotypeActomyosinMembrane ProteinsMyosin Type IIPARK7 protein, mouseProtein Deglycase DJ-1RETREG2 protein, human

Identifiers

PMID29097687
PMCPMC5668354

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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.