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Familial Frameshift SRY Mutation Inherited from a Mosaic Father with Testicular Dysgenesis Syndrome

CHU Nantes, Service de Génétique Médicale (B.I., M.G., A.D., C.L.C.), Service de Chirurgie Infantile (C.C., M.-D.L.), Clinique Médiale Pédiatrique (S.B.), and Service d’Oncologie Pédiatrique (N.C., B.C.), 44000 Nantes, France; Service d’Hormonologie (F.P., C.S.), Hôpital Lapeyronie, CHU Montpellier, F-34295 Montpellier, France; Unité de Génétique Clinique (D.M.-C.), Centre Hospitalier du Mans, 72000 Le Mans, France; and INSERM, UMR915, CNRS, ERL3147, Université de Nantes (C.L.C.), 44035 Nantes, France

Address all correspondence and requests for reprints to: Dr. Cédric Le Caignec, M.D., Ph.D., Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, 9 Quai Moncousu, 44093 Nantes Cedex 1, France. E-mail: cedric.lecaignec{at}chu-nantes.fr.

Context: The SRY gene encodes a transcription factor responsible for initiating testis differentiation. Mutations in SRY almost always result in XY sex reversal with pure gonadal dysgenesis and an increased risk of gonadal tumor. Most of these mutations are de novo, affecting only one individual in a family. Only a small subset of mutations is shared between a phenotypically normal father and one or more of his affected children. Incomplete penetrance and somatic mosaicism are two hypotheses that may explain a normal phenotype in a father carrying a SRY mutation.

Patients and Results: We describe a family with two sisters with XY sex reversal and pure gonadal dysgenesis and a phenotypically normal brother. A novel constitutional frameshift SRY mutation was identified in both sisters and was absent in the brother. The single base pair deletion (c.71delA) led to a premature stop codon in position 60 of the protein, removing entirely the high-mobility group domain and the DNA-binding domain of SRY. The father of the three children presented with hypospadias; cryptorchidism; testicular seminoma and oligoasthenozoospermia, an association termed testicular dysgenesis syndrome (TDS); and the SRY mutation in a mosaic state in the peripheral blood and the tumor.

Conclusions: This observation of somatic and germinal mosaicism for a SRY mutation may explain the variable penetrance in some familial gonadal dysgenesis. Importantly, the present report is the first one describing the association of SRY mutation in a male with TDS. This suggests that mutations in a sex-determining gene may contribute to the pathogenesis of TDS.