Genetic analysis of the follicle stimulating hormone receptor gene in women with polycystic ovary syndrome

Francesco Orio, E. Ferrarini, T. Cascella, A. Dimida, S. Palomba, E. Gianetti, A. Colao, P. Agretti, P. Vitti, G. Lombardi, A. Pinchera, M. Tonacchera

Research output: Contribution to journalArticle

Abstract

This study was designed to assess the relationship between mutations in the FSH receptor (FSHr) gene and polycystic ovary syndrome (PCOS) in Italian women. The study population included 50 patients with PCOS and 50 age- and body mass index (BMI)-matched controls. A complete anthropometrical, hormonal and pelvic ultrasonographic evaluation was performed in all subjects. Genomic DNA was extracted from peripheral lymphocytes and then each exon of the FSHr gene was amplified by PCR. The mutation identified was cloned and the functional properties were studied after transient expression in COS-7 cells. Direct sequencing of exons 1-10 of the FSHr gene revealed the presence of a heterozygous AAT/ ATT mutation affecting the isoleucine residue at position 411, which was replaced by an asparagine, in the second transmembrane segment (I411N). This mutation was only found in one woman with PCOS and not in her parents. This mutation was not present in 50 age and BMI controls and in another 150 women not affected by PCOS. The functional study after transient expression in COS-7 cells revealed that this I411N had similar functional characteristics with respect to the wild type FSHr (wtFSHr). Genetic analyses of polymorphisms in the human FSHr gene were also performed. All 50 women with PCOS harbored the A307T polymorphic variant, 56% harbored N680S, 30% S6805 and 14% N680N polymorphisms. In conclusion, the present study demonstrates that mutations of the FSHr gene are rare in Italian women. The only mutation that we found does not appear to have any pathophysiological significance in PCOS.

Original languageEnglish
Pages (from-to)975-982
Number of pages8
JournalJournal of Endocrinological Investigation
Volume29
Issue number11
Publication statusPublished - Dec 2006

Fingerprint

FSH Receptors
Polycystic Ovary Syndrome
Mutation
Genes
COS Cells
Exons
Body Mass Index
Human Follicle Stimulating Hormone
Isoleucine
Asparagine
Parents
Lymphocytes
Polymerase Chain Reaction
DNA

Keywords

  • FSH-receptor gene
  • Gene mutation
  • Hyperandrogenism
  • Insulin resistance
  • Polycystic ovary syndrome (PCOS)

ASJC Scopus subject areas

  • Endocrinology

Cite this

Orio, F., Ferrarini, E., Cascella, T., Dimida, A., Palomba, S., Gianetti, E., ... Tonacchera, M. (2006). Genetic analysis of the follicle stimulating hormone receptor gene in women with polycystic ovary syndrome. Journal of Endocrinological Investigation, 29(11), 975-982.

Genetic analysis of the follicle stimulating hormone receptor gene in women with polycystic ovary syndrome. / Orio, Francesco; Ferrarini, E.; Cascella, T.; Dimida, A.; Palomba, S.; Gianetti, E.; Colao, A.; Agretti, P.; Vitti, P.; Lombardi, G.; Pinchera, A.; Tonacchera, M.

In: Journal of Endocrinological Investigation, Vol. 29, No. 11, 12.2006, p. 975-982.

Research output: Contribution to journalArticle

Orio, F, Ferrarini, E, Cascella, T, Dimida, A, Palomba, S, Gianetti, E, Colao, A, Agretti, P, Vitti, P, Lombardi, G, Pinchera, A & Tonacchera, M 2006, 'Genetic analysis of the follicle stimulating hormone receptor gene in women with polycystic ovary syndrome', Journal of Endocrinological Investigation, vol. 29, no. 11, pp. 975-982.
Orio F, Ferrarini E, Cascella T, Dimida A, Palomba S, Gianetti E et al. Genetic analysis of the follicle stimulating hormone receptor gene in women with polycystic ovary syndrome. Journal of Endocrinological Investigation. 2006 Dec;29(11):975-982.
Orio, Francesco ; Ferrarini, E. ; Cascella, T. ; Dimida, A. ; Palomba, S. ; Gianetti, E. ; Colao, A. ; Agretti, P. ; Vitti, P. ; Lombardi, G. ; Pinchera, A. ; Tonacchera, M. / Genetic analysis of the follicle stimulating hormone receptor gene in women with polycystic ovary syndrome. In: Journal of Endocrinological Investigation. 2006 ; Vol. 29, No. 11. pp. 975-982.
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AU - Gianetti, E.

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