Jenderny J, Röhrborn G
Hum Genet. 1987 Aug;76(4):385-8. doi: 10.1007/BF00272450.
A modified technique has been developed for the visualization of the chromosomes in human sperm. The cytogenetic analysis of 129 G-banded human sperm metaphases of 6 normal donors showed an incidence of structural and numerical chromosome abnormalities of 7.8%. Two out of 129 spermatozoa were aneuploid (1.6%). The frequency of sperms with chromatid-type aberrations was 2.3% (3/129). Chromosome-type aberrations were found in 5 out of 129 (3.9%) spermatozoa. X to Y ratio did not differ significantly from the expected one-to-one ratio. Twenty-six sperm complements from a patient 18-20 months after testes exposure to 30 Gy were examined. A significant increase of numerical and structural chromosome abnormalities was not observed. Chromatid-type aberrations were found in two sperm complements (7.7%) and chromosome-type aberrations in one sperm complement (3.9%). The cytogenetic analysis of 15 human sperms from a cancer patient 26 months after chemotherapy showed an increased frequency of aberrant sperm complements (33.4%). One chromatid-type (6.7%), three chromosome-type aberrations (20.0%) and one (6.7%) hyperploid sperm complement could be observed. The sample size is still too small to answer the question whether chemical mutagens may increase the frequency of chromosomal abnormalities in human sperm.
已开发出一种改良技术用于观察人类精子中的染色体。对6名正常供体的129个经G带染色的人类精子中期相进行细胞遗传学分析,结果显示结构和数目染色体异常的发生率为7.8%。129个精子中有2个为非整倍体(1.6%)。具有染色单体型畸变的精子频率为2.3%(3/129)。在129个精子中有5个(3.9%)发现有染色体型畸变。X与Y的比例与预期的一对一比例无显著差异。对一名患者在睾丸接受30 Gy照射后18 - 20个月的26个精子核型进行了检查。未观察到数目和结构染色体异常的显著增加。在两个精子核型中发现有染色单体型畸变(7.7%),在一个精子核型中发现有染色体型畸变(3.9%)。对一名癌症患者化疗后26个月的15个人类精子进行细胞遗传学分析,结果显示异常精子核型的频率增加(33.4%)。可观察到一个染色单体型畸变(6.7%)、三个染色体型畸变(20.0%)和一个超倍体精子核型(6.7%)。样本量仍然太小,无法回答化学诱变剂是否会增加人类精子中染色体异常频率这一问题。