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对精子发生至关重要的Y染色体区域。

The Y chromosome region essential for spermatogenesis.

作者信息

Nakahori Y, Kuroki Y, Komaki R, Kondoh N, Namiki M, Iwamoto T, Toda T, Kobayashi K

机构信息

Department of Human Genetics, School of International Health, University of Tokyo, Japan.

出版信息

Horm Res. 1996;46 Suppl 1:20-3. doi: 10.1159/000185175.

Abstract

We analyzed DNA from 153 Japanese men with azoospermia or severe oligozoospermia whose Y chromosomes were cytogenetically normal. A total of 23 loci on the Y chromosome were examined: 15 loci within interval 6 including YRRM1 and DAZ, and 8 loci outside interval 6. Microdeletions were observed in 20 individuals. All deletions involved at least one locus within interval 6. The YRRM1 gene deletion was found in 4 patients, of whom 2 also lacked the SMCY gene. The remaining 16 individuals shared the absence of 10 loci between DYS7C and DYS239 including the DAZ gene. Among them, 13 were azoospermic while 3 showed a little sperm production, indicating that the common deletion resulted in phenotypic diversity. Since there is no region commonly deleted in all patients, azoospermia caused by deletion of the Y chromosome long arm may be genetically heterogeneous.

摘要

我们分析了153名患有无精子症或严重少精子症且Y染色体细胞遗传学正常的日本男性的DNA。共检测了Y染色体上的23个位点:6号区间内的15个位点,包括YRRM1和DAZ,以及6号区间外的8个位点。在20名个体中观察到微缺失。所有缺失均涉及6号区间内至少一个位点。在4名患者中发现了YRRM1基因缺失,其中2名患者也缺乏SMCY基因。其余16名个体在DYS7C和DYS239之间共有10个位点缺失,包括DAZ基因。其中,13名患者无精子,3名患者有少量精子产生,这表明常见缺失导致了表型多样性。由于并非所有患者都存在共同缺失区域,因此Y染色体长臂缺失导致的无精子症可能在遗传上是异质性的。

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