R-spondins are a recently characterized small family of growth factors. Here we show that human R-spondin1 (RSPO1) is the gene disrupted in a recessive syndrome characterized by XX sex reversal, palmoplantar hyperkeratosis and predisposition to squamous cell carcinoma of the skin. Our data show, for the first time, that disruption of a single gene can lead to complete female-to-male sex reversal in the absence of the testis determining gene, SRY.

R-spondin1 is essential in sex determination, skin differentiation and malignancy

CAMERINO, GIOVANNA
2006-01-01

Abstract

R-spondins are a recently characterized small family of growth factors. Here we show that human R-spondin1 (RSPO1) is the gene disrupted in a recessive syndrome characterized by XX sex reversal, palmoplantar hyperkeratosis and predisposition to squamous cell carcinoma of the skin. Our data show, for the first time, that disruption of a single gene can lead to complete female-to-male sex reversal in the absence of the testis determining gene, SRY.
2006
Molecular Biology & Genetics considers all aspects of basic and applied genetics, including molecular genetics, prokaryotic and eukaryotic gene expression, mechanisms of mutagenesis, structure, function and regulation of genetic material. Also included are resources concerned with clinical genetics, patterns of inheritance, genetic cause, and screening and treatment of disease. Resources dealing specifically with developmentally regulated gene expression, or with signal transduction pathways that modulate gene expression at the cellular level are excluded and are covered in the Cell and Developmental Biology category.
Sì, ma tipo non specificato
Inglese
Internazionale
STAMPA
38
11
1304
1309
Cited in News and Views in the same publication. Nat Genet. 2006 Nov;38(11):1233-4.
R-spondin1; sex determination; skin differentiation
9
info:eu-repo/semantics/article
262
P., Parma; O., Radi; V., Vidal; Chaboissier, M. C.; E., Dellambra; S., Valentini; L., Guerral; A., Schedl; Camerino, Giovanna
1 Contributo su Rivista::1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/102159
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