• PMID: 25502990
• Gene Name: NR5A1
• Condition: 46,XY is gonadal dysgenesis
• Association: In conclusion, we report on a novel hypomorphic NR5A1 mutation, which may be associated with the phenotype of the family.
• Mutation: c.910G>A, p.E304K
• Sex: Male
• Infertility type: Male infertility
• Other associated phenotypes: 46,XY is gonadal dysgenesis

Fertility preservation in a family with a novel NR5A1 mutation

Yagi H, Takagi M, Kon M, Igarashi M, Fukami M, Hasegawa Y.

The common phenotype of nuclear receptor superfamily 5, group A, member 1 (NR5A1) gene mutations in 46,XY is gonadal dysgenesis without adrenal deficiency. Though the phenotype of gonadal dysgenesis is variable, ranging from complete female to normal male genitalia, an asymptomatic 46,XY male is rare. Preserved fertility has so far been described in only three affected 46,XY males with different mutations, but no functional analysis of these mutations has been performed. Here, we report on male siblings with hypospadias and their asymptomatic father in whom we identified a heterozygous NR5A1 mutation of c.910G>A, p.E304K. Western blotting and subcellular localization revealed no significant difference between the wild type (WT) and E304K. Electrophoretic mobility shift assay experiments showed that E304K abrogated DNA-binding ability. E304K reduced transactivation and had no dominant negative effect. In conclusion, we report on a novel hypomorphic NR5A1 mutation, which may be associated with the phenotype of the family. FAU - Yagi, Hiroko AU - Yagi H AD - Division of Genetic Research, Tokyo Metropolitan Children's Medical Center, Tokyo 183-8561, Japan. FAU - Takagi, Masaki AU - Takagi M FAU - Kon, Masafumi AU - Kon M FAU - Igarashi, Maki AU - Igarashi M FAU - Fukami, Maki AU - Fukami M