Evidence map›Paper›PMID 36473458›Full record

ArticleDevelopmental cell2022

Nodal signaling establishes a competency window for stochastic cell fate switching.

Andrew D Economou, Luca Guglielmi, Philip East, Caroline S Hill

Open access · hybridAbstract read
In one paragraph

Article in Developmental cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Transcriptional divergence of the zebrafishbioRxiv : the preprint server for biology · 2026
    Article
  2. Review
  3. Disrupted developmental signaling induces novel transcriptional states.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Optogenetic control of Nodal signaling patterns.Development (Cambridge, England) · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Optogenetic control of Nodal signaling patterns.bioRxiv : the preprint server for biology · 2024
    Article
  10. Article
  11. Context-dependent TGFβ family signalling in cell fate regulation.Nature reviews. Molecular cell biology · 2023
    Review
  12. Article
  13. Article
  14. Article
  15. 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

4 authors at 1 institution in 1 country.

Andrew D EconomouDevelopmental Signalling Laboratory, The Francis Crick Institute, London, UK.
Luca GuglielmiDevelopmental Signalling Laboratory, The Francis Crick Institute, London, UK.
Philip EastBioinformatics and Biostatistics Facility, The Francis Crick Institute, London, UK.
Caroline S HillDevelopmental Signalling Laboratory, The Francis Crick Institute, London, UK. Electronic address: caroline.hill@crick.ac.uk.
The Francis Crick Institute · GB

Funding

Cancer Research UK 15681Cancer Research UK CC2021Medical Research Council CC2021Wellcome Trust CC2021
6 · The paper itself

Abstract

Specification of the germ layers by Nodal signaling has long been regarded as an archetype of how graded morphogens induce different cell fates. However, this deterministic model cannot explain why only a subset of cells at the early zebrafish embryo margin adopt the endodermal fate, whereas their immediate neighbours, experiencing a similar signaling environment, become mesoderm. Combining pharmacology, quantitative imaging and single cell transcriptomics, we demonstrate that sustained Nodal signaling establishes a bipotential progenitor state from which cells can switch to an endodermal fate or differentiate into mesoderm. Switching is a random event, the likelihood of which is modulated by Fgf signaling. This inherently imprecise mechanism nevertheless leads to robust endoderm formation because of buffering at later stages. Thus, in contrast to previous deterministic models of morphogen action, Nodal signaling establishes a temporal window when cells are competent to undergo a stochastic cell fate switch, rather than determining fate itself.

Indexed as

ZebrafishAnimalsendoderm specificationFGFmesoderm specificationmorphogen gradientNodalstochastic cell switching

Identifiers

PMID36473458
PMCPMC7615190
OpenAlexW4311587713

What Socratic 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 Socratic graph.