RESUMO

Mutations in the sex-determining region of the Y chromosome (the SRY gene) have been reported in low frequency in patients with 46,XY gonadal dysgenesis. We investigated 21 Brazilian 46,XY sex-reversed patients, who presented either complete or partial gonadal dysgenesis or embryonic testicular regression syndrome. Using Southern blotting, polymerase chain reaction, denaturing gradient gel electrophoresis and direct sequencing, we analyzed deletions and point mutations in the SRY gene. We found a missense mutation at codon 18 upstream of the 5' border of the HMG box of the SRY gene in one patient with partial gonadal dysgenesis. This variant sequence was also found in DNA obtained from blood and sperm cells of his father and in blood cells of his normal brother. The S18N mutation was not found in 50 normal males, ruling out the possibility of a common polymorphism. We identified a novel familial missense mutation (S18N) in the 5' non-HMG box of the SRY gene in 1 of 21 patients with 46,XY sex reversal.

Assuntos

Proteínas de Ligação a DNA/genética , Disgenesia Gonadal/genética , Proteínas de Grupo de Alta Mobilidade/genética , Proteínas Nucleares , Mutação Puntual , Processos de Determinação Sexual , Fatores de Transcrição , Adolescente , Adulto , Asparagina/genética , Pré-Escolar , Humanos , Cariotipagem , Masculino , Homologia de Sequência do Ácido Nucleico , Serina/genética , Proteína da Região Y Determinante do Sexo