Evidence map›Paper›PMID 26081573›Full record

ArticleDevelopment (Cambridge, England)2015

Tissue-specific roles of Fgfr2 in development of the external genitalia.

Marissa L Gredler, Ashley W Seifert, Martin J Cohn

Open access · greenAbstract read
In one paragraph

Article in Development (Cambridge, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 47 citations in OpenAlex.

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  12. Spatiotemporal map of key signaling factors during early penis development.Developmental dynamics : an official publication of the American Association of Anatomists · 2022
    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

3 authors at 2 institutions in 1 country.

Marissa L GredlerDepartment of Biology, UF Genetics Institute, University of Florida, PO Box 103610, Gainesville, FL 32611, USA.
Ashley W SeifertDepartment of Biology, UF Genetics Institute, University of Florida, PO Box 103610, Gainesville, FL 32611, USA.
Martin J CohnDepartment of Biology, UF Genetics Institute, University of Florida, PO Box 103610, Gainesville, FL 32611, USA Howard Hughes Medical Institute, Department of Molecular Genetics and Microbiology, University of Florida, PO Box 103610, Gainesville, FL 32611, USA mjcohn@ufl.edu.
University of Florida · USHoward Hughes Medical Institute · US

Funding

Targets of Endocrine Disruptors in External GenitaliaR01ES017099 · NIEHS · UNIVERSITY OF FLORIDA · PI COHN, MARTIN J · 2010 to 2014
$2.0M
Howard Hughes Medical InstituteNIEHS NIH HHS R01 ES017099NIEHS NIH HHS R01-ES017099
6 · The paper itself

Abstract

Congenital anomalies frequently occur in organs that undergo tubulogenesis. Hypospadias is a urethral tube defect defined by mislocalized, oversized, or multiple openings of the penile urethra. Deletion of Fgfr2 or its ligand Fgf10 results in severe hypospadias in mice, in which the entire urethral plate is open along the ventral side of the penis. In the genital tubercle, the embryonic precursor of the penis and clitoris, Fgfr2 is expressed in two epithelial populations: the endodermally derived urethral epithelium and the ectodermally derived surface epithelium. Here, we investigate the tissue-specific roles of Fgfr2 in external genital development by generating conditional deletions of Fgfr2 in each of these cell types. Conditional deletion of Fgfr2 results in two distinct phenotypes: endodermal Fgfr2 deletion causes mild hypospadias and inhibits maturation of a complex urethral epithelium, whereas loss of ectodermal Fgfr2 results in severe hypospadias and absence of the ventral prepuce. Although these cell type-specific mutants exhibit distinctive genital anomalies, cellular analysis reveals that Fgfr2 regulates epithelial maturation and cell cycle progression in the urethral endoderm and in the surface ectoderm. The unexpected finding that ectodermal deletion of Fgfr2 results in the most severe hypospadias highlights a major role for Fgfr2 in the developing genital surface epithelium, where epithelial maturation is required for maintenance of a closed urethral tube. These results demonstrate that urethral tubulogenesis, prepuce morphogenesis, and sexually dimorphic patterning of the lower urethra are controlled by discrete regions of Fgfr2 activity.

Indexed as

AnimalsCell AdhesionCell CycleCell ProliferationClitorisEctodermFemaleFibroblast Growth Factor 10Gene Expression Regulation, DevelopmentalHypospadiasMaleMiceMice, TransgenicOrganogenesisOrgan SpecificityPenisFgf10 protein, mouseFgfr2 protein, mouseFibroblast Growth Factor 10Receptor, Fibroblast Growth Factor, Type 2FgfGenitaliaMouseSexual differentiationTubulogenesisUrethra

Identifiers

PMID26081573
PMCPMC4483768
OpenAlexW2170962504

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.