Spermatogenesis in a man with complete deletion of USP9Y

N Engl J Med. 2009 Feb 26;360(9):881-5. doi: 10.1056/NEJMoa0806218.

Abstract

Deletions in the azoospermia factor region AZFa on the human Y chromosome and, more specifically, in the region that encompasses the ubiquitin-specific peptidase 9, Y-linked gene USP9Y have been implicated in infertility associated with oligospermia and azoospermia. We have characterized in detail a deletion in AZFa that results in an absence of USP9Y in a normospermic man and his brother and father. The association of this large deletion with normal fertility shows that USP9Y, hitherto considered a candidate gene for infertility and azoospermia, does not have a key role in male reproduction. These results suggest that it may not be necessary to consider USP9Y when screening the Y chromosome of infertile or subfertile men for microdeletions.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Azoospermia / genetics
  • Chromosomes, Human, Y
  • DEAD-box RNA Helicases / genetics
  • Fertility / genetics
  • Gene Deletion*
  • Gene Expression
  • Genes, Y-Linked*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Infertility, Male / genetics*
  • Male
  • Microscopy, Electron, Transmission
  • Minor Histocompatibility Antigens
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sperm Count
  • Spermatogenesis / genetics*
  • Spermatozoa / ultrastructure
  • Ubiquitin Thiolesterase / genetics*

Substances

  • Minor Histocompatibility Antigens
  • USP9Y protein, human
  • Ubiquitin Thiolesterase
  • DDX3Y protein, human
  • DEAD-box RNA Helicases