Benet J, Martin R H
Department de Biologica Cellular i Fisiologia, Facultat de Medicina, Universitat Autonoma de Barcelona, Bellaterra, Spain.
Hum Genet. 1988 Apr;78(4):313-5. doi: 10.1007/BF00291725.
Human sperm chromosomes from a 47,XYY male were examined using the direct method of sperm chromosome analysis with two modifications in the semen processing. A total of 75 sperm complements was karyotyped and all of these contained one sex chromosome. The percentages of X- and Y-bearing sperm were 53% and 47%, respectively. There were 10 sperm with autosomal chromosomal abnormalities. The frequencies of numerical (4.0%), structural (10.6%), and total (13.3%) abnormalities were not significantly different from the frequencies observed in normal donors in our laboratory. Our results do not support the suggestion that XYY males have an increased risk of aneuploid progeny as a result of secondary non-disjunction or interchromosomal effects. They do support the hypothesis that one Y chromosome is eliminated in the germ cells of XYY males. However since our study provides the first information on sperm chromosomes in an XYY male, further studies on other XYY men are required.
采用精子染色体分析直接法并对精液处理进行了两项改进,对一名47,XYY男性的人类精子染色体进行了检查。共对75个精子核型进行了分析,所有这些精子都含有一条性染色体。含X染色体和Y染色体的精子百分比分别为53%和47%。有10个精子存在常染色体异常。数值异常(4.0%)、结构异常(10.6%)和总异常(13.3%)的频率与我们实验室正常供体中观察到的频率无显著差异。我们的结果不支持以下观点:由于二次不分离或染色体间效应,XYY男性产生非整倍体后代的风险增加。它们确实支持这样的假设:在XYY男性的生殖细胞中,一条Y染色体会被消除。然而,由于我们的研究提供了关于XYY男性精子染色体的首个信息,因此需要对其他XYY男性进行进一步研究。