• PMID: 10402373
• Gene Name: DAZ1
• Condition: Infertility
• Association: Deletions in the AZFc region involving the DAZ gene were observed in severe hypospermatogenesis suggesting that deletions of this region are not sufficient to cause complete loss of the spermatogenic line. The RBM gene was observed to have a very minor ro
• Mutation: Deletions in the Y chromosome
• Population size: 360
• Population details: 180 ( 55 azoospermic and Sertoli cell-only, 85 severe oligozoospermia and hypospermatogenesis, 20 moderate oligozoospermia and hypospermatogenesis, 20 mild oligospermia and hypospermatogenesis ), 50 azoospermic and severely oligozoospermic men with known
• Sex: Male
• Infertility type: Male infertility
• Associated genes: RBM, DFFRY
• Other associated phenotypes: Azoospermic , Sertoli cell-only, severe oligozoospermia , hypospermatogenesis,

Human male infertility and Y chromosome deletions: role of the AZF-candidate genes DAZ, RBM and DFFRY

Ferlin A, Moro E, Garolla A, Foresta C.

Microdeletions in Yq11 overlapping three distinct 'azoospermia factors' (AZFa-c) represent the aetiological factor of 10-15% of idiopathic azoospermia and severe oligozoospermia, with higher prevalence in more severe testiculopathies, such as Sertoli cell-only syndrome. Using a PCR-based screening, we analysed Yq microdeletions in 180 infertile patients affected by idiopathic Sertoli cell-only syndrome and different degrees of hypospermatogenesis, compared with 50 patients with known causes of testicular alteration, 30 with obstructive azoospermia, and 100 normal fertile men. In idiopathic severe testiculopathies (Sertoli cell-only syndrome and severe hypospermatogenesis), a high prevalence of microdeletions (34.5% and 24.7% respectively) was found, while milder forms were not associated with Yq alteration. No deletions were found in testiculopathies of known aetiology, obstructive azoospermia, normal fertile men and male relatives of patients with deletions. Deletions in the AZFc region involving the DAZ gene were the most frequent finding and they were more often observed in severe hypospermatogenesis than in Sertoli cell-only syndrome, suggesting that deletions of this region are not sufficient to cause complete loss of the spermatogenic line. Deletions in AZFb involving the RBM gene were less frequently detected and there was no correlation with testicular phenotype, with an apparent minor role for such gene in spermatogenesis. The DFFRY gene was absent in a fraction of patients, making it a candidate AZFa gene. Our data suggest that larger deletions involving more than one AZF-candidate gene are associated with a more severe testicular phenotype. FAU - Ferlin, A AU - Ferlin A AD - Department of Medical and Surgical Sciences, Clinica Medica 3, University of Padova, Via Ospedale 105, 35128 Padova, Italy. FAU - Moro, E AU - Moro E FAU - Garolla, A AU - Garolla A