Gene dosage of DAX-1, determining in sexual differentiation: duplication of DAX-1 in two sisters with gonadal dysgenesis

Mary García-Acero, Mónica Molina, Olga Moreno, Andrea Ramirez, Catalina Forero, Camila Céspedes, Juan Carlos Prieto, Jaime Pérez, Fernando Suárez-Obando, Adriana Rojas

Producción: Contribución a una revistaArtículorevisión exhaustiva

21 Citas (Scopus)

Resumen

Two sisters phenotypically normal females, presenting with tumor abdominal mass with histopathological findings of teratoma and gonadoblastoma associated to 46,XY male-to-female sex reversal syndrome, secondary to a duplication in DAX-1, possibly inherited of maternal gonadal mosaicism. Copy number variation and functional effects of the duplication were done by MLPA multiplex ligation-dependent probe amplification and real time PCR. DAX-1, also known as dosage sensitive sex reversal gene (DSS), is considered the most likely candidate gene involved in XY gonadal dysgenesis when overexpressed. The excess of DAX-1 gene disturbs testicular development by down regulation of SF-1, WT1, and SOX9. This is the first report of 46,XY sex reversal in two siblings who have a maternally inherited duplication of DAX-1 associated with reduced levels of expression of downstream genes as SOX9-SF1.

Idioma originalInglés
Páginas (desde-hasta)2971-2978
Número de páginas8
PublicaciónMolecular Biology Reports
Volumen46
N.º3
DOI
EstadoPublicada - jun. 2019

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