Ma S, Ferguson K A, Arsovska S, Moens P, Chow V
Department of Obstetrics and Gynaecology, University of British Columbia, Vancouver, British Columbia, Canada.
Hum Reprod. 2006 Apr;21(4):980-5. doi: 10.1093/humrep/dei428. Epub 2005 Dec 22.
Studies using gene-linkage analysis have suggested that abnormal recombination during meiosis may lead to the production of aneuploid gametes; however, there is little direct evidence of a link between the two in human males. We analysed spermatocytes in the pachytene stage from a man with extremely high aneuploidy rates in his sperm. Testicular tissue specimens of the infertile man and two vasectomy reversals were processed with immuofluorescent techniques to visualize synaptonemal complex and recombination foci and fluorescent in situ hybridization on spermatocytes and sperm with probes for chromosomes 13, 21, 18, X and Y. We observed no recombination between sex chromosomes in the infertile man, while in two controls, we observed recombination rates of 79.3 and 81.0% between the sex chromosomes. This was associated with a total sex aneuploidy rate of 41.61% in testicular sperm of the infertile man (0.44 and 0.62% in two controls). Recombination on chromosome 21 was reduced in the infertile man, with 10.62% of spermatocytes showing no recombination (0 and 1.67% in two controls), as well as chromosome 13, with 53.98% having < or =1 recombination foci (22.05 and 21.67% in two controls). This was associated with increased aneuploidy for those chromosomes. Chromosome 18 aneuploidy was slightly increased, although there was no apparent decrease in recombination. These results provide the first evidence of both recombination and non-disjunction abnormalities in the same individual. This is also the only reported case of an infertile man who shows no recombination between the sex chromosomes, despite the formation of the sex body.
使用基因连锁分析的研究表明,减数分裂过程中的异常重组可能导致非整倍体配子的产生;然而,在人类男性中,几乎没有两者之间存在联系的直接证据。我们分析了一名精子非整倍体率极高的男性粗线期的精母细胞。对该不育男性以及两名输精管复通者的睾丸组织标本进行免疫荧光技术处理,以观察联会复合体和重组位点,并对精母细胞和精子进行荧光原位杂交,使用针对13号、21号、18号、X和Y染色体的探针。我们观察到该不育男性的性染色体之间没有重组,而在两名对照者中,我们观察到性染色体之间的重组率分别为79.3%和81.0%。这与该不育男性睾丸精子中41.61%的总性染色体非整倍体率相关(两名对照者分别为0.44%和0.62%)。不育男性中21号染色体上的重组减少,10.62%的精母细胞未出现重组(两名对照者分别为0和1.67%),13号染色体也是如此,53.98%的细胞具有≤1个重组位点(两名对照者分别为22.05%和21.67%)。这与这些染色体的非整倍体增加相关。18号染色体的非整倍体略有增加,尽管重组没有明显减少。这些结果首次证明了同一个体中存在重组和不分离异常。这也是唯一一例报道的不育男性,尽管形成了性体,但性染色体之间没有重组。