Evidence map›Paper›PMID 33376218›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Post-transcriptional tuning of FGF signaling mediates neural crest induction.

Jacqueline Copeland, Marcos Simoes-Costa

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. 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
1.2field-weighted citation impact, top 22% 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, 24 citations in OpenAlex.

  1. Core microRNAs regulate neural crest delamination and condensation in the developing trigeminal ganglion.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  2. Article
  3. Ectomesenchymal identity emerges via relief ofbioRxiv : the preprint server for biology · 2025
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  5. Review
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  7. Post-transcriptional regulation in cranial neural crest cells expands developmental potential.Proceedings of the National Academy of Sciences of the United States of America · 2023
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  11. Review
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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

2 authors at 1 institution in 1 country.

Jacqueline CopelandDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14850.
Marcos Simoes-CostaDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14850 simoescosta@cornell.edu.
Cornell University · US

Funding

Spatial Control of Pattern Formation in Early Vertebrate DevelopmentDP2HD102043 · NICHD · CORNELL UNIVERSITY · PI SIMOES-COSTA, MARCOS · 2019 to 2019
$2.4M
Genomic control of neural crest identity by signaling systemsR01DE028576 · NIDCR · CORNELL UNIVERSITY · PI SIMOES-COSTA, MARCOS · 2019 to 2023
$1.9M
NICHD NIH HHS DP2 HD102043NIDCR NIH HHS R01 DE028576
6 · The paper itself

Abstract

Ectodermal patterning is required for the establishment of multiple components of the vertebrate body plan. Previous studies have demonstrated that precise combinations of extracellular signals induce distinct ectodermal cell populations, such as the neural crest and the neural plate. Yet, we still lack understanding of how the response to inductive signals is modulated to generate the proper transcriptional output in target cells. Here we show that posttranscriptional attenuation of fibroblast growth factor (FGF) signaling is essential for the establishment of the neural crest territory. We found that neural crest progenitors display elevated expression of DICER, which promotes enhanced maturation of a set of cell-type-specific miRNAs. These miRNAs collectively target components of the FGF signaling pathway, a central player in the process of neural induction in amniotes. Inactivation of this posttranscriptional circuit results in a fate switch, in which neural crest cells are converted into progenitors of the central nervous system. Thus, the posttranscriptional attenuation of signaling systems is a prerequisite for proper segregation of ectodermal cell types. These findings demonstrate how posttranscriptional repression may alter the activity of signaling systems to generate distinct spatial domains of progenitor cells.

Indexed as

Signal TransductionTranscription, GeneticAnimalsCell LineageChick EmbryoEctodermFibroblast Growth FactorsGene Expression Regulation, DevelopmentalMicroRNAsModels, BiologicalNeural CrestRibonuclease IIIStem CellsFibroblast Growth FactorsMicroRNAsRibonuclease IIIectodermFGF signalingmiRNAsneural crestsignaling systems

Identifiers

PMID33376218
PMCPMC7777031
OpenAlexW3116005160

What OpenQuestion holds

Textmetadata
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.