Acar H, Kilinç M, Cora T, Aktan M, Taşkapu H
Department of Medical Genetics, Selçuk University, Faculty of Medicine, Konya, Turkey.
Urol Int. 2000;64(4):202-8. doi: 10.1159/000030531.
We studied the frequency of aneuploidy in sperm nuclei of six infertile men with abnormal semen profile and normal karyotype, using fluorescence in situ hybridization (FISH) with DNA probes for chromosomes 8, 10, X and Y. The control group consisted of four healthy fertile men with normal karyotype and semen profiles. The purpose of this study was to determine whether there are differences between infertile male donors and control donors for: (1) the incidence of sex chromosome aneuploidy, and (2) the number of disomies for chromosomes 8, and 10 cosegregating with chromosomes X and Y. FISH analysis showed no significant differences of sex ratios of the sperm nuclei in and between infertile and control groups. The most significant abnormalities in the infertile group were clusters of sperm nuclei bearing XY and XYY. In addition, the incidence of disomic sperm nuclei for chromosomes 8 and 10 consegregating with sex chromosomes was not significantly different between the patient and control groups, nor within them. However, the total frequency of aneuploid sperm nuclei was significantly different between the infertile group and the control group. We observed a significant excess of sperm nuclei bearing chromosome 10 along with disomy for chromosome Y (10YY). In conclusion, our results from FISH analysis demonstrate a significantly increased frequency of aneuploidy for the sex chromosomes in sperm nuclei from infertile men. Therefore it may be concluded that infertility is a risk factor for sex chromosome aneuploidy in sperm nuclei.
我们使用针对8号、10号、X和Y染色体的DNA探针进行荧光原位杂交(FISH),研究了6名精液异常但核型正常的不育男性精子核中的非整倍体频率。对照组由4名核型和精液指标正常的健康有生育能力的男性组成。本研究的目的是确定不育男性供体与对照供体在以下方面是否存在差异:(1)性染色体非整倍体的发生率,以及(2)与X和Y染色体共分离的8号和10号染色体的二体数目。FISH分析显示,不育组与对照组内部及之间精子核的性别比例无显著差异。不育组中最显著的异常是携带XY和XYY的精子核簇。此外,患者组与对照组之间以及组内,与性染色体共分离的8号和10号染色体的二体精子核发生率均无显著差异。然而,不育组与对照组之间非整倍体精子核的总频率存在显著差异。我们观察到携带10号染色体并伴有Y染色体二体(10YY)的精子核显著增多。总之,我们的FISH分析结果表明,不育男性精子核中性染色体的非整倍体频率显著增加。因此,可以得出结论,不育是精子核中性染色体非整倍体的一个风险因素。