Evidence map›Paper›PMID 29720666›Full record

ArticleNature communications2018

P53 and mTOR signalling determine fitness selection through cell competition during early mouse embryonic development.

Sarah Bowling, Aida Di Gregorio, Margarida Sancho, Sara Pozzi, Marieke Aarts, Massimo Signore, Michael D Schneider, Juan Pedro Martinez-Barbera, Jesús Gil, Tristan A Rodríguez

Erratum issuedAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing 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

65 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Endocytic Control of Cell-Autonomous and Non-Cell-Autonomous Functions of p53.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  6. Critical role of cell competition in gliomagenesis.bioRxiv : the preprint server for biology · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Relationship of PSC to embryos: Extending and refining capture of PSC lines from mammalian embryos.BioEssays : news and reviews in molecular, cellular and developmental biology · 2024
    Review

5 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Sarah BowlingBritish Heart Foundation Centre for Research Excellence, National Heart and Lung Institute, Imperial Centre for Translational and Experimental Medicine, Imperial College London, Hammersmith Hospital Campus, Du Cane Road, London, W12 0NN, UK.
Aida Di GregorioBritish Heart Foundation Centre for Research Excellence, National Heart and Lung Institute, Imperial Centre for Translational and Experimental Medicine, Imperial College London, Hammersmith Hospital Campus, Du Cane Road, London, W12 0NN, UK.
Margarida SanchoBritish Heart Foundation Centre for Research Excellence, National Heart and Lung Institute, Imperial Centre for Translational and Experimental Medicine, Imperial College London, Hammersmith Hospital Campus, Du Cane Road, London, W12 0NN, UK.
Sara PozziDevelopmental Biology and Cancer Programme, Newlife Birth Defects Research Centre, UCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1N, UK.
Marieke AartsCell Proliferation Group, MRC London Institute of Medical Sciences (LMS), Du Cane Road, London, W12 0NN, UK.
Massimo SignoreDevelopmental Biology and Cancer Programme, Newlife Birth Defects Research Centre, UCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1N, UK.
Michael D SchneiderBritish Heart Foundation Centre for Research Excellence, National Heart and Lung Institute, Imperial Centre for Translational and Experimental Medicine, Imperial College London, Hammersmith Hospital Campus, Du Cane Road, London, W12 0NN, UK.ORCID http://orcid.org/0000-0001-9645-1938
Juan Pedro Martinez-BarberaDevelopmental Biology and Cancer Programme, Newlife Birth Defects Research Centre, UCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1N, UK.
Jesús GilCell Proliferation Group, MRC London Institute of Medical Sciences (LMS), Du Cane Road, London, W12 0NN, UK. jesus.gil@imperial.ac.uk.
Tristan A RodríguezBritish Heart Foundation Centre for Research Excellence, National Heart and Lung Institute, Imperial Centre for Translational and Experimental Medicine, Imperial College London, Hammersmith Hospital Campus, Du Cane Road, London, W12 0NN, UK. tristan.rodriguez@imperial.ac.uk.ORCID http://orcid.org/0000-0002-3415-8493

Funding

Medical Research Council G0901467Medical Research Council MC_U120085810Medical Research Council MR/N009371/1Medical Research Council MR/P018467/1
6 · The paper itself

Abstract

Ensuring the fitness of the pluripotent cells that will contribute to future development is important both for the integrity of the germline and for proper embryogenesis. Consequently, it is becoming increasingly apparent that pluripotent cells can compare their fitness levels and signal the elimination of those cells that are less fit than their neighbours. In mammals the nature of the pathways that communicate fitness remain largely unknown. Here we identify that in the early mouse embryo and upon exit from naive pluripotency, the confrontation of cells with different fitness levels leads to an inhibition of mTOR signalling in the less fit cell type, causing its elimination. We show that during this process, p53 acts upstream of mTOR and is required to repress its activity. Finally, we demonstrate that during normal development around 35% of cells are eliminated by this pathway, highlighting the importance of this mechanism for embryonic development.

Indexed as

Signal TransductionAnimalsCell CommunicationCell DifferentiationCell LineCell ProliferationEmbryo, MammalianEmbryonic DevelopmentGene Expression ProfilingGene Expression Regulation, DevelopmentalMiceMice, Inbred C57BLMice, Inbred CBAMice, KnockoutMouse Embryonic Stem CellsTOR Serine-Threonine KinasesmTOR protein, mouseTOR Serine-Threonine KinasesTrp53 protein, mouseTumor Suppressor Protein p53

Identifiers

PMID29720666
PMCPMC5932021

What OpenQuestion holds

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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.