Evidence map›Paper›PMID 32735816›Full record

ArticleCurrent biology : CB2020

Mechanochemical Crosstalk Produces Cell-Intrinsic Patterning of the Cortex to Orient the Mitotic Spindle.

Andrea Dimitracopoulos, Pragya Srivastava, Agathe Chaigne, Zaw Win, Roie Shlomovitz, Oscar M Lancaster, Maël Le Berre, Matthieu Piel, Kristian Franze, Guillaume Salbreux and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Current biology : CB, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.6field-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

14 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. On the origin of the nucleus: a hypothesis.Microbiology and molecular biology reviews : MMBR · 2023
    Review
  4. Competition and Synergy of Arp2/3 and Formins in Nucleating Actin Waves.bioRxiv : the preprint server for biology · 2023
    Article
  5. Article
  6. Article
  7. Article
  8. Mitotic outcomes and errors in fibrous environments.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  9. Article
  10. Article
  11. Spindle reorientation in response to mechanical stress is an emergent property of the spindle positioning mechanisms.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  12. Review
  13. Review
  14. 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

11 authors at 4 institutions in 3 countries.

Andrea DimitracopoulosDepartment of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3DY, UK; MRC Laboratory for Molecular Cell Biology, University College London, Gower Street, London WC1E 6BT, UK. Electronic address: ad865@cam.ac.uk.
Pragya SrivastavaThe Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Agathe ChaigneMRC Laboratory for Molecular Cell Biology, University College London, Gower Street, London WC1E 6BT, UK.
Zaw WinMRC Laboratory for Molecular Cell Biology, University College London, Gower Street, London WC1E 6BT, UK.
Roie ShlomovitzMRC Laboratory for Molecular Cell Biology, University College London, Gower Street, London WC1E 6BT, UK; Department of Chemical Physics, The Weizmann Institute of Science, PO Box 26, Rehovot 76100, Israel.
Oscar M LancasterMRC Laboratory for Molecular Cell Biology, University College London, Gower Street, London WC1E 6BT, UK.
Maël Le BerreInstitut Curie, PSL Research University, CNRS, UMR 144, Paris 75005, France.
Matthieu PielInstitut Curie, PSL Research University, CNRS, UMR 144, Paris 75005, France.
Kristian FranzeDepartment of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3DY, UK.
Guillaume SalbreuxThe Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK; Institute for the Physics of Living Systems, University College London, Gower Street, London WC1E 6BT, UK. Electronic address: guillaume.salbreux@crick.ac.uk.
Buzz BaumMRC Laboratory for Molecular Cell Biology, University College London, Gower Street, London WC1E 6BT, UK; Institute for the Physics of Living Systems, University College London, Gower Street, London WC1E 6BT, UK. Electronic address: b.baum@ucl.ac.uk.
MRC Laboratory for Molecular Cell Biology · GBCentre National de la Recherche Scientifique · FRThe Francis Crick Institute · GBUniversity of Cambridge · GB

Funding

Biotechnology and Biological Sciences Research Council BB/R009732/1Cancer Research UK 17343Cancer Research UK 21144Cancer Research UK 23335Cancer Research UK 28276Cancer Research UK C1529/A17343Cancer Research UK C1529/A9786Cancer Research UK FC001317Medical Research Council FC001317Medical Research Council MC_CF12266Wellcome Trust 201334/Z/16/ZWellcome Trust FC001317
6 · The paper itself

Abstract

Proliferating animal cells are able to orient their mitotic spindles along their interphase cell axis, setting up the axis of cell division, despite rounding up as they enter mitosis. This has previously been attributed to molecular memory and, more specifically, to the maintenance of adhesions and retraction fibers in mitosis [1-6], which are thought to act as local cues that pattern cortical Gαi, LGN, and nuclear mitotic apparatus protein (NuMA) [3, 7-18]. This cortical machinery then recruits and activates Dynein motors, which pull on astral microtubules to position the mitotic spindle. Here, we reveal a dynamic two-way crosstalk between the spindle and cortical motor complexes that depends on a Ran-guanosine triphosphate (GTP) signal [12], which is sufficient to drive continuous monopolar spindle motion independently of adhesive cues in flattened human cells in culture. Building on previous work [1, 12, 19-23], we implemented a physical model of the system that recapitulates the observed spindle-cortex interactions. Strikingly, when this model was used to study spindle dynamics in cells entering mitosis, the chromatin-based signal was found to preferentially clear force generators from the short cell axis, so that cortical motors pulling on astral microtubules align bipolar spindles with the interphase long cell axis, without requiring a fixed cue or a physical memory of interphase shape. Thus, our analysis shows that the ability of chromatin to pattern the cortex during the process of mitotic rounding is sufficient to translate interphase shape into a cortical pattern that can be read by the spindle, which then guides the axis of cell division.

Indexed as

Mechanotransduction, CellularMitosisDyneinsHeLa CellsHumansMicrotubulesSignal TransductionSpindle ApparatusDyneinscellcomputational modelLGNlong axismechanochemical modelmicrotubulesmitotic roundingmitotic spindlemonopolar spindleRan-GTPspindle orientation

Identifiers

PMID32735816
PMCPMC7521479
OpenAlexW3045546692

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.