Mokánszki Attila, Ujfalusi Anikó, Gombos Éva, Balogh István
Department of Laboratory Medicine, Division of Clinical Genetics, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
J Hum Reprod Sci. 2018 Oct-Dec;11(4):329-336. doi: 10.4103/jhrs.JHRS_12_18.
The aim of this study was to establish the Y chromosome microdeletion and partial AZFc microdeletion/duplication frequency firstly in East Hungarian population and to gain information about the molecular mechanism of the heterogeneous phenotype identified in males bearing partial AZFc deletions and duplications.
Exactly determined sequences of azoospermia factor (AZF) region were amplified. Lack of amplification was detected for deletion. To determine the copy number of and genes, we performed a quantitative analysis. The primers flank an insertion/deletion difference, which permitted the polymerase chain reaction products to be separated by polyacrylamide gel electrophoresis.
Mann-Whitney/Wilcoxon two-sample test, Kruskal-Wallis test, and two-sample t-probe were used for statistical analysis.
AZFbc deletion was detected only in the azoospermic cases; AZFc deletion occurred significantly more frequently among azoospermic patients, than among oligozoospermic males. The frequency of gr/gr deletions was significantly higher in the oligozoospermic patients than in the normospermic group. The b2/b3 deletion and partial duplications were not different among our groups, while b1/b3 deletion was found only in the azoospermic group. In infertile males and in normozoospermic controls, similar Y haplogroup distribution was detected with the highest frequency of haplogroup P. The gr/gr deletion with haplogroup was more frequent in the oligozoospermic group than in the normozoospermic males. The b2/b3 deletion with E haplogroup was the most frequent, found only in the normozoospermic group.
Y microdeletion screening has prognostic value and can affect the clinical therapy. In case of Y chromosome molecular genetic aberrations, genetic counseling makes sense also for other males in the family because these types of aberrations are transmittable (from father to son 100% transmission).
本研究的目的是首先确定匈牙利东部人群中Y染色体微缺失和部分AZFc微缺失/重复的频率,并获取有关携带部分AZFc缺失和重复的男性中鉴定出的异质表型分子机制的信息。
对无精子症因子(AZF)区域的精确确定序列进行扩增。检测到扩增缺失则表明存在缺失。为了确定 和 基因的拷贝数,我们进行了定量分析。引物侧翼存在插入/缺失差异,这使得聚合酶链反应产物能够通过聚丙烯酰胺凝胶电泳分离。
采用Mann-Whitney/Wilcoxon双样本检验、Kruskal-Wallis检验和双样本t检验进行统计分析。
仅在无精子症病例中检测到AZFbc缺失;AZFc缺失在无精子症患者中出现的频率明显高于少精子症男性。少精子症患者中gr/gr缺失的频率明显高于正常精子症组。b2/b3缺失和部分重复在我们的研究组之间没有差异,而b1/b3缺失仅在无精子症组中发现。在不育男性和正常精子症对照组中,检测到相似的Y单倍群分布,其中单倍群P的频率最高。少精子症组中带有单倍群的gr/gr缺失比正常精子症男性更常见。带有E单倍群的b2/b3缺失最常见,仅在正常精子症组中发现。
Y微缺失筛查具有预后价值,可影响临床治疗。对于Y染色体分子遗传异常的情况,对家族中的其他男性进行遗传咨询也有意义,因为这些类型的异常是可遗传的(从父亲到儿子100%遗传)。