Evidence map›Paper›PMID 25809880›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2015

Wnt8a and Wnt3a cooperate in the axial stem cell niche to promote mammalian body axis extension.

Thomas J Cunningham, Sandeep Kumar, Terry P Yamaguchi, Gregg Duester

Open access · bronzeAbstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

23 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
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  8. Marine life science & technology · 2021
    Article
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  11. Review
  12. Development (Cambridge, England) · 2019
    Article
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  14. Observational
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  19. The Multiple Roles of FGF Signaling in the Developing Spinal Cord.Frontiers in cell and developmental biology · 2017
    Review
  20. Article
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 2 institutions in 1 country.

Thomas J CunninghamDevelopment, Aging, and Regeneration Program, Sanford-Burnham Medical Research Institute, La Jolla, California.
Sandeep KumarDevelopment, Aging, and Regeneration Program, Sanford-Burnham Medical Research Institute, La Jolla, California.
Terry P YamaguchiCancer and Developmental Biology Laboratory, NCI-Frederick, National Institutes of Health, Frederick, Maryland.
Gregg DuesterDevelopment, Aging, and Regeneration Program, Sanford-Burnham Medical Research Institute, La Jolla, California.
Sanford Burnham Prebys Medical Discovery Institute · USFrederick National Laboratory for Cancer Research · US

Funding

The Role of Wnt Genes in Vertebrate Development and CancerZIABC010345 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI YAMAGUCHI, TERENCE · 2009 to 2025
$23.3M
Generation of Retinoid Signals During DevelopmentR01GM062848 · NIGMS · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI DUESTER, GREGG L · 2002 to 2015
$4.6M
NIGMS NIH HHS GM062848NIGMS NIH HHS R01 GM062848
6 · The paper itself

Abstract

backgroundVertebrate body axis extension occurs in a head-to-tail direction from a caudal progenitor zone that responds to interacting signals. Wnt/β-catenin signaling is critical for generation of paraxial mesoderm, somite formation, and maintenance of the axial stem cell pool. Body axis extension requires Wnt8a in lower vertebrates, but in mammals Wnt3a is required, although the anterior trunk develops in the absence of Wnt3a.

resultsWe examined mouse Wnt8a(-/-) and Wnt3a(-/-) single and double mutants to explore whether mammalian Wnt8a contributes to body axis extension and to determine whether a posterior growth function for Wnt8a is conserved throughout the vertebrate lineage. We find that caudal Wnt8a is expressed only during early somite stages and is required for normal development of the anterior trunk in the absence of Wnt3a. During this time, we show that Wnt8a and Wnt3a cooperate to maintain Fgf8 expression and prevent premature Sox2 up-regulation in the axial stem cell niche, critical for posterior growth. Similar to Fgf8, Wnt8a requires retinoic acid (RA) signaling to restrict its caudal expression boundary and possesses an upstream RA response element that binds RA receptors.

conclusionsThese findings provide new insight into interaction of caudal Wnt-FGF-RA signals required for body axis extension.

Indexed as

Abnormalities, MultipleAlcohol OxidoreductasesAnimalsBody PatterningConserved SequenceFibroblast Growth Factor 8GastrulationGene Expression Regulation, DevelopmentalHomeodomain ProteinsIntercellular Signaling Peptides and ProteinsMiceMice, KnockoutPhenotypeReceptors, Retinoic AcidResponse ElementsSignal TransductionAlcohol OxidoreductasesFgf8 protein, mouseFibroblast Growth Factor 8Homeodomain ProteinsIntercellular Signaling Peptides and ProteinsReceptors, Retinoic AcidSox2 protein, mouseSOXB1 Transcription Factorstrans-retinol dehydrogenaseTretinoinUncx4.1 protein, mouseWnt3A ProteinWnt3a protein, mouseWnt8a protein, mouseWnt Proteinsbody axis extensionFgf8mouseRdh10retinoic acidsomitogenesisWnt3aWnt8a

Identifiers

PMID25809880
PMCPMC4449298
OpenAlexW1500747401

What OpenQuestion holds

Textmetadata
LicenceTDM
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.