Human Molecular Genetics Advance Access published online on August 7, 2006
Human Molecular Genetics, doi:10.1093/hmg/ddl198
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1 Department of Clinical Physiopathology, Andrology Unit, University of Florence, Viale Pieraccini 6, 50139 Florence, Italy
* To whom correspondence should be addressed. Deletions of the AZoospermia Factor Regions (AZF) of the Y chromosome are associated with severe spermatogenic failure and represent the most frequent molecular genetic cause of azoospermia and severe oligozoospermia. The exact role of the candidate AZF genes is largely unknown due to both the extreme rarity of naturally occurring AZF gene specific mutations and the lack of functional assays. Here, we report the fine characterization of two different deletions in the USP9Y gene (one of the two candidate genes in the AZFa region), which have been transmitted through natural conception in two unrelated families. The associated mild testicular phenotype, in both cases, is in sharp contrast with that of the two previously reported infertile patients bearing a mutation of the same gene. In conclusion, to date the USP9Y gene has been considered as one of the major Y-linked spermatogenesis genes, based on both its position within the AZFa region and previous reports that correlated USP9Y mutation to severe spermatogenic failure and infertility. This view is now substantially changed since our findings clearly demonstrate that during human spermatogenesis, USP9Y is more likely a fine tuner that improves efficiency, rather than a provider of an essential function. More importantly, the observed natural conceptions suggest that the protein is not required for the final sperm maturation process or for the acquisition of sperm fertilizing ability, providing a new perspective on the role played by the USP9Y gene in male fertility.
Received April 10, 2006
Revised July 19, 2006
Accepted July 27, 2006
Article
Natural transmission of USP9Y gene mutations: a new perspective on the role of AZFa genes in male fertility
Csilla Krausz 1 *, Selene Degl'Innocenti 1, Francesca Nuti 1, Annamaria Morelli 1, Federica Felici 1, Mauro Sansone 2, Gennaro Varriale 3, and Gianni Forti 1
2 U.O.C. di Molecular Genomics and Biochemistry ASL n.1 Naples, Italy
3 Department of Molecular and Cellular Pathology "Federico II" Via S. Pansini, 5, Naples, Italy
Csilla Krausz, E-mail: E-mail: c.krausz{at}dfc.unifi.it
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