Department of Genetics and Reproduction, Veterinary Research Institute, Hudcova 70, Brno, Czech Republic.
J Assist Reprod Genet. 2013 Mar;30(3):391-405. doi: 10.1007/s10815-012-9921-9. Epub 2013 Jan 15.
To analyse relationships between semen parameters, sperm chromatin integrity and frequencies of chromosomally unbalanced, disomic and diploid sperm in 13 Robertsonian and 37 reciprocal translocation carriers and to compare the results with data from 10 control donors.
Conventional semen analysis, Sperm Chromatin Structure Assay and FISH with probes for chromosomes involved in the individual translocations and for chromosomes X, Y, 7, 8, 13, 18 and 21.
Normal semen parameters were found in 30.8 % of Robertsonian and 59.5 % of reciprocal translocation carriers. The rates of unbalanced sperm were 12.0 % in Robertsonian and 55.1 % in reciprocal translocation carriers with no difference between normospermic patients and those showing altered semen parameters. Significantly increased frequencies of spermatozoa showing defects in chromatin integrity and condensation, aneuploidy for chromosomes not involved in a translocation and diploidy were detected in translocation carriers with abnormal semen parameters. Normospermic reciprocal translocation carriers showed an increase in chromosome 13 disomy compared to the control group. There was no relationship between gametic and somatic aneuploidy in 12 translocation carriers studied by FISH on sperm and lymphocytes. The frequency of motile sperm was negatively correlated with the frequency of sperm showing disomy, diploidy and defective chromatin condensation.
Abnormal semen parameters can serve as indicators of an additional risk of forming spermatozoa with defective chromatin and aneuploidy in translocation carriers.
分析 13 例罗伯逊易位和 37 例相互易位携带者的精液参数、精子染色质完整性与染色体非整倍体、双着丝粒和二倍体精子的频率之间的关系,并与 10 名对照供体的结果进行比较。
常规精液分析、精子染色质结构分析和用涉及个体易位的染色体探针以及 X、Y、7、8、13、18 和 21 号染色体探针进行荧光原位杂交(FISH)。
30.8%的罗伯逊易位携带者和 59.5%的相互易位携带者具有正常的精液参数。非平衡精子的比率在罗伯逊易位携带者中为 12.0%,在相互易位携带者中为 55.1%,在正常精子参数的患者和精液参数改变的患者之间没有差异。在精液参数异常的易位携带者中,发现精子染色质完整性和浓缩缺陷、未涉及易位的染色体非整倍体以及二倍体精子的频率显著增加。与对照组相比,正常精液参数的相互易位携带者的染色体 13 三体率增加。在通过 FISH 在精子和淋巴细胞中研究的 12 例易位携带者中,未发现配子和体细胞非整倍体之间存在关系。有活力精子的频率与显示非整倍体、二倍体和染色质浓缩缺陷的精子频率呈负相关。
异常的精液参数可作为易位携带者形成染色质和染色体非整倍体缺陷精子的附加风险的指标。