[Analysis of a novel mutation of AR gene in a patient featuring mild androgen insensitivity syndrome].

OBJECTIVE To investigate the clinical and molecular genetics characteristics of a patient with mild androgen insensitivity syndrome (MAIS). METHODS Clinical data of the patient was collected, and DNA was isolated from peripheral blood sample. Eight exons of AR gene were amplified by PCR with specific primers and directly sequenced by Sanger method. The results were compared with standard sequences from GenBank. Online Polyphen-2 software was applied to predict the effect of mutation on the protein function and compare the conservation of the sequence at the mutation site in various species. The exon of the AR gene containing the mutated site was analyzed in 90 unrelated normal males using PCR and restrictive digestion with Sfa NI. RESULTS Sequence analysis has detected a novel missense mutation in codon 176 of exon 1 (Ser176Arg) of the AR gene. Analysis with polyphen-2 software has indicated the codon to be highly conserved across various species, and that the S176A mutation has caused damage to the protein structure and function (prediction score=0.999). The same mutation was not detected in 90 healthy males. CONCLUSION The S176A mutation of the AR gene may contribute to the mild androgen insensitivity syndrome.