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PMID 18579508
Gene Name DAZ1
Condition Infertility
Association The study concludes that the findings indicate that some monophyletic Y chromosomes may be associated with predisposition to specific subtypes of partial AZFc deletion and adverse effect on spermatogenesis
Mutation AZFc deletions
Population size 2189
Population details 269non-AZFc-deleted men with unknown spermatogenic status as controls, 634 men with normozoospermia (57 partial AZFc deletion (19 de novo deletion, 29 inherited, 9 samples from relatives absent)), 1286 azoospermic/oligozoospermic (157 partial AZFc deleted
Age 21-39yrs
Sex Male
Infertility type Male infertility
Associated genes CDY1
Other associated phenotypes Azoospermia, Oligozoospermia, cryptozoospermic, asthenoteratozoospermic


Y chromosome haplogroups may confer susceptibility to partial AZFc deletions and deletion effect on spermatogenesis impairment

Yang Y, Ma M, Li L, Zhang W, Chen P, Ma Y, Liu Y, Tao D, Lin L, Zhang S.

BACKGROUND: Partial AZFc deletions related to testis-specific gene families are common mutations of the Y chromosome, but their contribution to spermatogenic impairment is still unresolved, and the risk factors for the formation of the deletions remain unknown. With this in mind, we investigated the possible association between Y chromosome haplogroups and predisposition to partial AZFc deletions and their effect on spermatogenesis in a Chinese population. METHODS: The haplogrouping was carried out using 12 polymorphic loci on the Y chromosome in 269 non-AZFc-deleted controls with an unknown spermatogenic status and 214 men with a partial AZFc deletion defined by the absence of the sequence-tagged site and sequence family variant loss of the DAZ and CDY1 genes. In the latter group, 57 men had normozoospermia and 157 men had azoo/oligozoospermia. Among these, 122 had a de novo partial AZFc deletion. RESULTS: Y haplogroup distribution differed significantly between men with a de novo partial AZFc deletion and the control group, and between men with a specific subtype of the partial AZFc deletions and the control group. Further, partial AZFc deletions gave rise to spermatogenesis impairment in some Y haplogroups. CONCLUSIONS: The findings indicate that some monophyletic Y chromosomes may be associated with predisposition to specific subtypes of partial AZFc deletion and adverse effect on spermatogenesis. Although these deletions were not confirmed with gene dosage analysis, the results suggest that Y chromosome background is an important factor that affects partial AZFc deletion formation and its contribution to spermatogenic failure. FAU - Yang, Yuan AU - Yang Y AD - Department of Medical Genetics, West China Hospital, West China Medical School and State Key Laboratory of Biotherapy, Sichuan University, Gaopeng Street, Keyuan Road 4, Chengdu, Sichuan 610041, People's Republic of China. FAU - Ma, Mingyi AU - Ma M FAU - Li, Lei AU - Li L FAU - Zhang, Wei AU - Zhang W FAU - Chen, Pu AU - Chen P FAU - Ma, Yongxin AU - Ma Y FAU - Liu, Yunqiang AU - Liu Y FAU - Tao, Dachang AU - Tao D FAU - Lin, Li AU - Lin L