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一名USP9Y完全缺失男性的精子发生情况

Spermatogenesis in a man with complete deletion of USP9Y.

作者信息

Luddi Alice, Margollicci Maria, Gambera Laura, Serafini Francesca, Cioni Maddalena, De Leo Vincenzo, Balestri Paolo, Piomboni Paola

机构信息

Department of Pediatrics, Obstetrics, and Reproductive Medicine, University of Siena, Italy.

出版信息

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.

摘要

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。

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