Brandriff B F, Gordon L A, Moore D, Carrano A V
Lawrence Livermore National Laboratory, University of California 94550.
Cytogenet Cell Genet. 1988;47(1-2):29-36. doi: 10.1159/000132500.
We have analyzed structural aberrations in 5,000 sperm chromosome complements obtained from 20 men over a 5-yr period by fusion of human sperm with hamster eggs. Detailed data are presented on 366 abnormal cells with 379 analyzable breakpoints. The frequency of cells with structural aberrations ranged from 1.9% to 14.5% among donors; this interindividual variability was statistically significant (p less than 0.0001). In contrast, repeat samples from individual men showed no significant variation over time. The number of sperm chromosome sets processed per hamster egg had no effect on the frequency with which structural aberrations occurred, nor were sperm chromosome abnormalities altered by varying capacitation or culture conditions. The spectrum of structural aberrations observed in human sperm chromosomes and a chi-square analysis of breakpoints based on DNA content are presented. Although human sperm chromosome abnormalities were visualized with a cross-species system, we believe that they represent an inherent, biologically significant phenomenon.
我们在5年时间里,通过人精子与仓鼠卵融合,对从20名男性获取的5000个精子染色体组进行了结构畸变分析。给出了366个异常细胞及379个可分析断点的详细数据。供体中结构畸变细胞的频率在1.9%至14.5%之间;这种个体间差异具有统计学意义(p小于0.0001)。相比之下,来自个体男性的重复样本随时间未显示出显著变化。每个仓鼠卵处理的精子染色体组数对结构畸变发生的频率没有影响,改变获能或培养条件也不会改变精子染色体异常情况。展示了在人类精子染色体中观察到的结构畸变谱以及基于DNA含量的断点卡方分析。尽管人类精子染色体异常是在跨物种系统中观察到的,但我们认为它们代表了一种内在的、具有生物学意义的现象。