Evidence map›Paper›PMID 36222828›Full record

ArticleThe Journal of cell biology2022

Nuclear tension controls mitotic entry by regulating cyclin B1 nuclear translocation.

Margarida Dantas, Andreia Oliveira, Paulo Aguiar, Helder Maiato, Jorge G Ferreira

Open access · greenAbstract read
In one paragraph

Article in The Journal of cell biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
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  11. Mechanical stress during confined migration causes aberrant mitoses and c-MYC amplification.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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  17. Mechanomemory in protein diffusivity of chromatin and nucleoplasm after force cessation.Proceedings of the National Academy of Sciences of the United States of America · 2023
    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

5 authors at 2 institutions in 1 country.

Margarida DantasInstituto de Investigação e Inovação em Saúde (i3S), Universidade do Porto, Porto, Portugal.
Andreia OliveiraInstituto de Investigação e Inovação em Saúde (i3S), Universidade do Porto, Porto, Portugal.
Paulo AguiarInstituto de Investigação e Inovação em Saúde (i3S), Universidade do Porto, Porto, Portugal.ORCID 0000-0003-4164-5713
Helder MaiatoInstituto de Investigação e Inovação em Saúde (i3S), Universidade do Porto, Porto, Portugal.ORCID 0000-0002-6200-9997
Jorge G FerreiraInstituto de Investigação e Inovação em Saúde (i3S), Universidade do Porto, Porto, Portugal.ORCID 0000-0001-6802-3696
Universidade do Porto · PTi3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As cells prepare to divide, they must ensure that enough space is available to assemble the mitotic machinery without perturbing tissue homeostasis. To do so, cells undergo a series of biochemical reactions regulated by cyclin B1-CDK1 that trigger cytoskeletal reorganization and ensure the coordination of cytoplasmic and nuclear events. Along with the biochemical events that control mitotic entry, mechanical forces have recently emerged as important players in cell-cycle regulation. However, the exact link between mechanical forces and the biochemical pathways that control mitotic progression remains unknown. Here, we identify a tension-dependent signal on the nucleus that sets the time for nuclear envelope permeabilization (NEP) and mitotic entry. This signal relies on actomyosin contractility, which unfolds the nucleus during the G2-M transition, activating the stretch-sensitive cPLA2 on the nuclear envelope and regulating the nuclear translocation of cyclin B1. Our data demonstrate how nuclear tension during the G2-M transition contributes to timely and efficient mitotic spindle assembly and prevents chromosomal instability.

Indexed as

Active Transport, Cell NucleusCyclin B1MitosisActomyosinCDC2 Protein KinaseCell NucleusChromosomal InstabilityNuclear EnvelopePhospholipases A2, CytosolicSpindle ApparatusActomyosinCDC2 Protein KinaseCyclin B1Phospholipases A2, Cytosolic

Identifiers

PMID36222828
PMCPMC9565158
OpenAlexW4304693800

What Socratic 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 Socratic graph.