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与无精子症相关的Y染色体上一个新的热休克基因的缺失。

A deletion of a novel heat shock gene on the Y chromosome associated with azoospermia.

作者信息

Vinci Giovanna, Raicu Florina, Popa Luis, Popa Olivia, Cocos Relu, McElreavey Ken

机构信息

Reproduction, Fertility and Populations, Institut Pasteur, 25 rue du Dr Roux, 75724 Paris Cedex 15, France.

出版信息

Mol Hum Reprod. 2005 Apr;11(4):295-8. doi: 10.1093/molehr/gah153. Epub 2005 Feb 25.

Abstract

Deletions of the Y chromosome are a significant cause of spermatogenic failure. Three major deletion intervals have been defined and termed AZFa, AZFb and AZFc. Here, we report an unusual case of a proximal AZFb deletion that includes the Y chromosome palindromic sequence P4 and a novel heat shock factor (HSFY). This deletion neither include the genes EIF1AY, RPS4Y2 nor copies of the RBMY1 genes. The individual presented with idiopathic azoospermia. We propose that deletions of the testis-specific HSFY gene family may be a cause of unexplained cases of idiopathic male infertility. This deletion would not have been detected using current protocols for Y chromosome microdeletion screens, therefore we recommend that current screening protocols be extended to include this region and other palindrome sequences that contain genes expressed specifically in the testis.

摘要

Y染色体缺失是精子发生失败的一个重要原因。已确定三个主要缺失区间,分别称为AZFa、AZFb和AZFc。在此,我们报告一例不寻常的近端AZFb缺失病例,该缺失包括Y染色体回文序列P4和一个新的热休克因子(HSFY)。此缺失既不包括EIF1AY、RPS4Y2基因,也不包括RBMY1基因的拷贝。该个体表现为特发性无精子症。我们提出,睾丸特异性HSFY基因家族的缺失可能是特发性男性不育症不明原因病例的一个原因。使用当前的Y染色体微缺失筛查方案无法检测到这种缺失,因此我们建议将当前的筛查方案扩展到包括该区域以及其他包含在睾丸中特异性表达的基因的回文序列。

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