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PMID 10956550
Gene Name DAZ1
Condition Infertility
Association The study suggest that the Y chromosome genes BPY2, CDY1 and DAZ are not essential for sustained fertility and that rare alleles of autosomal or Xlinked loci can suppress the infertility associated with absence of AZFc
Mutation AZFc - deleted Y chromosome lacking DAZ, BYP2, CDY1
Population size 4
Population details 3 infertile
Sex Male
Infertility type Male infertility
Associated genes BYP2, CDY1


The human Y chromosome genes BPY2, CDY1 and DAZ are not essential for sustained fertility

Saut N, Terriou P, Navarro A, Lévy N, Mitchell MJ.

Deletions of the AZFc interval of the human Y chromosome are found in >5% of male patients with idiopathic infertility and are associated with a severely reduced sperm count. The most common deletion type is large (>1 Mb) and removes members of the Y-borne testis-specific gene families of BPY2, CDY1, DAZ, PRY, RBMY2 and TTY2, which are candidate AZF genes. Four exceptional individuals who have transmitted a large AZFc deletion naturally to their infertile sons have, however, been described. In three cases, transmission was to an only son, but in the fourth case a Y chromosome, shown to be deleted for all copies of DAZ, was transmitted from a father to his four infertile sons. Here we present a second family of this latter type and demonstrate that an AZFc-deleted Y chromosome lacking not only DAZ, but also BPY2 and CDY1, has been transmitted from a father to his three infertile sons. Polymerase chain reaction (PCR) and Southern blot analyses revealed no difference in the size of the AZFc deletion in the father and his sons. We propose that the father carries rare alleles of autosomal or X-linked loci which suppress the infertility that is frequently associated with the absence of AZFc. FAU - Saut, N AU - Saut N AD - Inserm U.491, Faculté de Médecine, 27 Boulevard Jean Moulin, 13385 Marseille cedex 05, France. FAU - Terriou, P AU - Terriou P FAU - Navarro, A AU - Navarro A FAU - Lévy, N AU - Lévy N