Premature Termination Mutation (772Glu→Stop) in the Hormone-Binding Domain of the Androgen Receptor in a Patient with the Receptor-Negative Form of Complete Androgen Insensitivity Syndrome

[摘要] References(20)Cited-By(1)We have characterized the androgen receptor in a Japanese infant with complete androgen insensitivity syndrome (or androgen resistance), and have investigated the molecular basis. Androgen binding was undetectable in cultured genital skin fibroblasts from this patient by whole-cell androgen receptor binding assay. Sequence analysis of the entire coding region of the androgen receptor gene from this patient revealed a single nucleotide substitution (G→T) at nucleotide position 2676 in exon E (or 5), resulting in conversion of glutamine codon (GAG) to amber stop codon (TAG) at amino acid position 772 within the hormone-binding domain of the androgen receptor. This premature termination mutation (or nonsense mutation), introducing a truncated androgen receptor that lacks most of its androgen binding capacity, is thought to cause the receptor-negative form of complete androgen insensitivity syndrome in this patient.

[学科分类] 内分泌与代谢学

[关键词] Androgen receptor;Complete androgen insensitivity syndrome;Receptor-negaive form;Premature termination mutation;Constitutive transcriptional activity