Mercier S, Morel F, Roux C, Clavequin M C, Bresson J L
Service de Cytogénétique, Immunocytologie, Biologie du Développement et de la Reproduction, Hôpital Saint Jacques, Besançon, France.
Mol Hum Reprod. 1996 Jul;2(7):485-8. doi: 10.1093/molehr/2.7.485.
The sex chromosomes in spermatozoa of a 47,XYY fertile male were analysed simultaneously by dual fluorescence in-situ hybridization (FISH), with two probes (pHY2.1 and pXBR). Of the 100000 cells analysed, 95179 spermatozoa (95.18%) exhibited one or more hybridization signals. Of the hybridized nuclei, 85.37% showed a normal sex chromosome constitution (37.37% X-bearing cells and 48.00% Y-bearing cells), with an X:Y ratio of 0.78:1. A total of 14.63% of the hybridized nuclei exhibited sex chromosome aneuploidy with a majority of XY- and YY-bearing spermatozoa (9.37 and 4.65% respectively). Even if the majority of spermatozoa have chromosomal haploidy, a large proportion of them exhibits numerical errors for the sex chromosomes. These observations raise questions about the commonly-admitted notions concerning the absence of chromosomal risk for XYY male offspring.
利用两种探针(pHY2.1和pXBR)通过双重荧光原位杂交(FISH)技术,对一名47,XYY可育男性精子中的性染色体进行了同步分析。在分析的100000个细胞中,95179个精子(95.18%)显示出一个或多个杂交信号。在杂交核中,85.37%呈现正常的性染色体组成(含X染色体的细胞占37.37%,含Y染色体的细胞占48.00%),X:Y比例为0.78:1。总共14.63%的杂交核表现出性染色体非整倍体,其中大多数是含XY和YY的精子(分别占9.37%和4.65%)。即使大多数精子具有染色体单倍体,但其中很大一部分在性染色体上存在数目错误。这些观察结果对关于XYY男性后代不存在染色体风险的普遍认可观念提出了质疑。