Evidence map›Paper›PMID 30958266›Full record

ArticleeLife2019

Transitions in cell potency during early mouse development are driven by Notch.

Sergio Menchero, Isabel Rollan, Antonio Lopez-Izquierdo, Maria Jose Andreu, Julio Sainz de Aja, Minjung Kang, Javier Adan, Rui Benedito, Teresa Rayon, Anna-Katerina Hadjantonakis and 1 more

Abstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Signaling pathway regulators in preimplantation embryos.Journal of molecular histology · 2024
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
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  11. Article
  12. Review
  13. Article
  14. Journey of the mouse primitive endoderm: from specification to maturation.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Nested information processing in the living world.Annals of the New York Academy of Sciences · 2021
    Review
  20. Review
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.

Sergio MencheroCentro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), Madrid, Spain.ORCID 0000-0003-4592-7259
Isabel RollanCentro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), Madrid, Spain.
Antonio Lopez-IzquierdoCentro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), Madrid, Spain.
Maria Jose AndreuCentro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), Madrid, Spain.
Julio Sainz de AjaCentro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), Madrid, Spain.
Minjung KangDevelopmental Biology Program, Sloan Kettering Institute, New York, United States.
Javier AdanCentro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), Madrid, Spain.
Rui BeneditoMolecular Genetics of Angiogenesis Group, Centro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), Madrid, Spain.
Teresa RayonCentro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), Madrid, Spain.
Anna-Katerina HadjantonakisDevelopmental Biology Program, Sloan Kettering Institute, New York, United States.ORCID 0000-0002-7580-5124
Miguel ManzanaresCentro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), Madrid, Spain.ORCID 0000-0003-4849-2836

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Mechanisms driving cell fate specification and morphogenesis in the blastocystR01HD094868 · NICHD · SLOAN-KETTERING INST CAN RESEARCH · PI ANNA-KATERINA HADJANTONAKIS · 2018 to 2026
$4.2M
Morphogenesis of mammalian gut endodermR01DK084391 · NIDDK · SLOAN-KETTERING INST CAN RESEARCH · PI HADJANTONAKIS, ANNA-KATERINA · 2009 to 2018
$4.1M
Ministerio de Economía y Competitividad BFU2015-72319-EXPMinisterio de Economía y Competitividad BFU2017-84914-PMinisterio de Economía y Competitividad SEV-2015-0505Ministerio de Economía y Competitividad SVP-2013-067930NCI NIH HHS P30 CA008748NICHD NIH HHS R01 HD094868NIDDK NIH HHS R01 DK084391NIH HHS NIH-P30CA008748NIH HHS NIH-R01DK084391NIH HHS NIH-R01HD094868
6 · The paper itself

Abstract

The Notch signalling pathway plays fundamental roles in diverse developmental processes in metazoans, where it is important in driving cell fate and directing differentiation of various cell types. However, we still have limited knowledge about the role of Notch in early preimplantation stages of mammalian development, or how it interacts with other signalling pathways active at these stages such as Hippo. By using genetic and pharmacological tools in vivo, together with image analysis of single embryos and pluripotent cell culture, we have found that Notch is active from the 4-cell stage. Transcriptomic analysis in single morula identified novel Notch targets, such as early naïve pluripotency markers or transcriptional repressors such as TLE4. Our results reveal a previously undescribed role for Notch in driving transitions during the gradual loss of potency that takes place in the early mouse embryo prior to the first lineage decisions.

Indexed as

Cell DifferentiationGene Expression Regulation, DevelopmentalSignal TransductionAnimalsGene Expression ProfilingMiceMorulaReceptors, NotchReceptors, NotchCdx2chromosomesdevelopmental biologygene expressionmorulamousenotchpreimplantation developmenttrophectoderm

Identifiers

PMID30958266
PMCPMC6486152

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.