AZF gene expression analysis in peripheral leukocytes and testicular cells from idiopathic infertility.

Ning-Hong Song, Chang-Jun Yin, Wei Zhang, Zuo-Min Zhuo, Guan-Xiong Ding, Jing Zhang, Li-Xin Hua, Hong-Fei Wu
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引用次数: 3

Abstract

The aim of this study was to assess the frequency of AZF microdeletions in peripheral leukocytes and testicular cells in Chinese men with idiopathic infertility. Expression in testicular cells was also determined. In this study, we screened 62 idiopathic infertile patients, in whom karyotype, sperm count and hormonal parameters were evaluated. Genomic DNA was extracted from the peripheral leukocytes. Molecular analysis was performed by two multiplex polymerase chain reactions (PCR) using a set of eight sequence tagged sites (STS) from 3 different regions of the Y chromosome. Total cellular RNA was extracted from the testicular tissue using a Trizol-method. Reverse Transcription (RT) reactions were performed to synthesize cDNA. Amplification of DFFRY, RBM and DAZ genes was performed to analyze their expression in testicular cells. In this cohort, we found 12 submicroscopic deletions (12/62, 19.4%). Nine patients (9/33, 27.2%) were detected in the azoospermic group and three (3/29, 10.3%) in the severe oligozoospermic group. RT-PCR analysis from testicular cells gave normal amplifications for SRY and DFFRY mRNA in 62 idiopathic patients; two patients were negative for RBM expression; no RBM and DAZ were detected for a case; 12 patients had no expression in the AZFc region involving the DAZ gene. Of 12 cases, three patients with normal PCR analysis of DAZ gene on genomic DNA showed no RT-PCR amplification for DAZ mRNA. The use of RT-PCR of specific spermatid expressed genes in conjunction with examining microdeletions using peripheral leukocytes is suggested to avoid the transmission of the Y chromosomal microdeletions from a father to a son via testicular sperm aspiration (TESE), intracytoplasmic sperm injection (JCSI).

特发性不育症患者外周血白细胞和睾丸细胞中AZF基因表达分析。
本研究的目的是评估中国男性特发性不育症患者外周血白细胞和睾丸细胞中AZF微缺失的频率。在睾丸细胞中的表达也被测定。在这项研究中,我们筛选了62例特发性不孕症患者,对他们的核型、精子数量和激素参数进行了评估。从外周血白细胞中提取基因组DNA。分子分析采用两种多重聚合酶链反应(PCR),利用来自Y染色体3个不同区域的8个序列标记位点(STS)进行。用trizol法从睾丸组织中提取细胞总RNA。通过逆转录(RT)反应合成cDNA。扩增DFFRY、RBM和DAZ基因,分析其在睾丸细胞中的表达。在这个队列中,我们发现了12个亚微观缺失(12/62,19.4%)。无精症组9例(9/33,27.2%),重度少精症组3例(3/29,10.3%)。62例特发性患者睾丸细胞RT-PCR分析显示SRY和DFFRY mRNA扩增正常;2例患者RBM表达阴性;1例未检出RBM和DAZ;12例患者AZFc区无DAZ基因表达。12例患者中,3例基因组DNA上DAZ基因PCR分析正常的患者未发现DAZ mRNA的RT-PCR扩增。建议使用RT-PCR对特定精子表达基因进行检测,同时使用外周白细胞检测微缺失,以避免通过睾丸精子抽吸(TESE)、胞浆内单精子注射(JCSI)将Y染色体微缺失从父亲传给儿子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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