Luddi Alice, Margollicci Maria, Gambera Laura, Serafini Francesca, Cioni Maddalena, De Leo Vincenzo, Balestri Paolo, Piomboni Paola
Department of Pediatrics, Obstetrics, and Reproductive Medicine, University of Siena, Italy.
N Engl J Med. 2009 Feb 26;360(9):881-5. doi: 10.1056/NEJMoa0806218.
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.
人类Y染色体上无精子症因子区域AZFa的缺失,更具体地说,包含泛素特异性肽酶9的Y连锁基因USP9Y所在区域的缺失,与少精子症和无精子症相关的不育症有关。我们详细描述了AZFa中的一个缺失,该缺失导致一名精子正常的男性及其兄弟和父亲中不存在USP9Y。这种大片段缺失与正常生育能力的关联表明,USP9Y迄今被认为是不育症和无精子症的候选基因,但在男性生殖中并不起关键作用。这些结果表明,在对不育或生育力低下男性的Y染色体进行微缺失筛查时,可能没有必要考虑USP9Y。