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Department of Endocrinology and Reproductive Medicine
Hôpital Necker (P.T., C.P., M.D., F.K.) Institut
Fédératif de Recherche (IFR-NEM) 75743 Paris
Cédex 15, France
INSERM U 135, Hormones, Gènes et
Reproduction et Laboratoire dHormonologie et Biologie
Moléculaire Hôpital de Bicêtre Assistance
Publique-Hôpitaux de Paris et Institut Fédératif
de Recherche IFR21 (I.B, G.M., A.D., E.M., M.M.) 94275 Le
Kremlin Bicêtre Cedex, France
INSERM U 407,
Faculté Médecine Lyon-Sud (A.G.) 69600 Oullins,
France
Department of Gynecology and Obstetrics (B.P.)
Hôpital Intercommunal de Créteil 94010 Creteil,
France
Department of Cytogenetics Hôpital
Necker-Enfants Malades (M.P.) 75743 Paris Cedex 15, France
Department of Gynecology and Obstetrics Hôpital Cochin
(J-R Z.) 75014 Paris, France
Premature ovarian failure occurs in almost 1% of women under age 40. Molecular alterations of the FSH receptor (FSHR) have recently been described. A first homozygous mutation of the FSHR was identified in Finland. More recently, we described two new mutations of the FSHR in a woman presenting a partial FSH-resistance syndrome (patient 1). We now report new molecular alterations of the FSHR in another woman (patient 2) who presented at the age of 19 with primary amenorrhea contrasting with normal pubertal development. She had high plasma FSH, and numerous ovarian follicles up to 3 mm in size were evidenced by ultrasonography. Histological and immunohistochemical examination of ovarian biopsies revealed the presence of a normal follicular development up to the antral stage and disruption at further stages.
DNA sequencing showed two heterozygous mutations: Asp224Val in the extracellular domain and Leu601Val in the third extracellular loop of FSHR. Cells transfected with expression vectors encoding the wild type or the mutated Leu601Val receptors bound hormone with similar affinity, whereas binding was barely detectable with the Asp224Val mutant. Confocal microscopy showed the latter to have an impaired targeting to the cell membrane. This was confirmed by its accumulation as a mannose-rich precursor. Adenylate cyclase stimulation by FSH of the Leu601Val mutant receptor showed a 12 ± 3% residual activity, whereas in patient 1 a 24 ± 4% residual activity was detected for the Arg573Cys mutant receptor. These results are in keeping with the fact that estradiol and inhibin B levels were higher in patient 1 and that stimulation with recombinant FSH did not increase follicular size, estradiol, or inhibin B levels in patient 2 in contrast to what was observed for patient 1. Thus, differences in the residual activity of mutated FSHR led to differences in the clinical, biological, and histological phenotypes of the patient.
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