Screening of FSH receptor gene in Argentine women with premature ovarian failure (POF)

• Autores: Sundblad, Victoria; Chiauzzi, Violeta; Escobar, Maria Eugenia; Dain, Liliana; Charreau, Eduardo H.
• Año de publicación: 2004
• Idioma: inglés
• Tipo de recurso: artículo
• Fuente: Molecular and Cellular Endocrinology 2004; 222(1-2):53-9.
• Materia: Insuficiencia Ovárica Primaria; Argentina
• Institución: Administración Nacional de Laboratorios e Institutos de Salud "Dr. Carlos G. Malbrán"

Fil: Sundblad, Victoria. Instituto de Biologı́a y Medicina Experimental (IBYME), Vuelta de Obligado 2490, C1428ADN Buenos Aires; Argentina.
Fil: Chiauzzi, Violeta. Instituto de Biologı́a y Medicina Experimental (IBYME), Vuelta de Obligado 2490, C1428ADN Buenos Aires; Argentina.
Fil: Escobar, Maria Eugenia. Centro de Investigaciones Endocrinológicas, Hospital de Niños Ricardo Gutierrez, Buenos Aires; Argentina.
Fil: Dain, Liliana. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina.
Fil: Charreau, Eduardo H. Instituto de Biologı́a y Medicina Experimental (IBYME), Vuelta de Obligado 2490, C1428ADN Buenos Aires; Argentina.
Diverse mutations in FSH-receptor (FSHR) gene have been described as possible cause of premature ovarian failure (POF). To investigate the presence of mutations and/or polymorphisms in FSHR gene, DNA from 20 POF, 5 of which were diagnosed as resistant ovary syndrome (ROS), and from 44 controls was isolated from peripheral lymphocytes. The complete coding sequence was analysed by PCR followed by SSCP, direct sequencing or restriction enzyme analysis. No mutations in FSHR gene were identified in the patients studied. The two already described polymorphisms in exon 10, A919G and A2039G, cosegregated in all the homozygous individuals, indicating that FSHR presents two isoforms: Ala307-Ser680 and Thr307-Asn680. OR results suggest that the 919G-2039G allelic variant or the homozygous genotype is not associated to disease risk. In addition, a heterozygous substitution T1022C (Val341Ala) was found in two control subjects. We suggest that mutations in FSHR gene are rare in women with POF in Argentine. Presence of a particular FSHR isoform does not appear to be associated with this disease.