Evidence map›Paper›PMID 25931449›Full record

ArticleScience (New York, N.Y.)2015

NEURODEVELOPMENT. Shared regulatory programs suggest retention of blastula-stage potential in neural crest cells.

Elsy Buitrago-Delgado, Kara Nordin, Anjali Rao, Lauren Geary, Carole LaBonne

Erratum issuedAbstract read
In one paragraph

Article in Science (New York, N.Y.), 2015. 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 97 papers.

0numbers the graph read from it
0cells of the map it votes in
97citing 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

97 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. A dual role for GLI3 signaling in neural crest development.Development (Cambridge, England) · 2026
    Article
  7. Article
  8. Article
  9. Review
  10. Ectomesenchymal identity emerges via relief ofbioRxiv : the preprint server for biology · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Epithelial-mesenchymal transition in tissue repair and degeneration.Nature reviews. Molecular cell biology · 2024
    Review
  17. Review
  18. Article
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Elsy Buitrago-DelgadoDepartment of Molecular Biosciences, Northwestern University, Evanston, IL 60208, USA.
Kara NordinDepartment of Molecular Biosciences, Northwestern University, Evanston, IL 60208, USA.
Anjali RaoDepartment of Molecular Biosciences, Northwestern University, Evanston, IL 60208, USA.
Lauren GearyDepartment of Molecular Biosciences, Northwestern University, Evanston, IL 60208, USA.
Carole LaBonneDepartment of Molecular Biosciences, Northwestern University, Evanston, IL 60208, USA. Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Evanston, IL 60208, USA. clabonne@northwestern.edu.

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
CELLULAR &MOLECULAR BASIS OF DISEASE TRAINING PROGRAMT32GM008061 · NIGMS · NORTHWESTERN UNIVERSITY · PI CARTHEW, RICHARD W. · 1985 to 2022
$17.1M
Resource CoreP40OD010997 · OD · MARINE BIOLOGICAL LABORATORY · PI Marko E Horb · 2012 to 2026
$13.1M
CARCINOGENESIS TRAINING PROGRAMT32CA009560 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Kathleen Janee Green · 1986 to 2026
$8.4M
Regulation of SoxE Function During Neural Crest FormationR01GM077288 · NIGMS · NORTHWESTERN UNIVERSITY · PI LABONNE, CAROLE · 2010 to 2013
$1.1M
SoxE regulation of Neural Crest DevelopmentF31DE021922 · NIDCR · NORTHWESTERN UNIVERSITY · PI NORDIN, KARA M · 2011 to 2014
$142k
NCI NIH HHS P30 CA060553NCI NIH HHS T32 CA009560NCI NIH HHS T32CA009560-24NIDCR NIH HHS F31 DE021922NIDCR NIH HHS F31DE021922NIGMS NIH HHS R01 GM077288NIGMS NIH HHS R01GM114058NIGMS NIH HHS T32 GM008061NIGMS NIH HHS T32GM008061NIH HHS P40 OD010997
6 · The paper itself

Abstract

Neural crest cells, which are specific to vertebrates, arise in the ectoderm but can generate cell types that are typically categorized as mesodermal. This broad developmental potential persists past the time when most ectoderm-derived cells become lineage-restricted. The ability of neural crest to contribute mesodermal derivatives to the bauplan has raised questions about how this apparent gain in potential is achieved. Here, we describe shared molecular underpinnings of potency in neural crest and blastula cells. We show that in Xenopus, key neural crest regulatory factors are also expressed in blastula animal pole cells and promote pluripotency in both cell types. We suggest that neural crest cells may have evolved as a consequence of a subset of blastula cells retaining activity of the regulatory network underlying pluripotency.

Indexed as

Gene Expression Regulation, DevelopmentalGene Regulatory NetworksAnimalsBlastulaEctodermEndodermNeural CrestNeurogenesisPluripotent Stem CellsTranscription FactorsXenopus laevisTranscription Factors

Identifiers

PMID25931449
PMCPMC4652794

What OpenQuestion holds

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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.