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Altered Crossover Distribution and Frequency in Spermatocytes of Infertile Men with Azoospermia

机译:不育症男性无精子症精子细胞中交叉分布和频率的改变

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摘要

During meiosis, homologous chromosomes pair to facilitate the exchange of DNA at crossover sites along the chromosomes. The frequency and distribution of crossover formation are tightly regulated to ensure the proper progression of meiosis. Using immunofluorescence techniques, our group and others have studied the meiotic proteins in spermatocytes of infertile men, showing that this population displays a reduced frequency of crossovers compared to fertile men. An insufficient number of crossovers is thought to promote chromosome missegregation, in which case the faulty cell may face meiotic arrest or contribute to the production of aneuploid sperm. Increasing evidence in model organisms has suggested that the distribution of crossovers may also be important for proper chromosome segregation. In normal males, crossovers are shown to be rare near centromeres and telomeres, while frequent in subtelomeric regions. Our study aims to characterize the crossover distribution in infertile men with non-obstructive (NOA) and obstructive azoospermia (OA) along chromosomes 13, 18 and 21. Eight of the 16 NOA men and five of the 21 OA men in our study displayed reduced crossover frequency compared to control fertile men. Seven NOA men and nine OA men showed altered crossover distributions on at least one of the chromosome arms studied compared to controls. We found that although both NOA and OA men displayed altered crossover distributions, NOA men may be at a higher risk of suffering both altered crossover frequencies and distributions compared to OA men. Our data also suggests that infertile men display an increase in crossover formation in regions where they are normally inhibited, specifically near centromeres and telomeres. Finally, we demonstrated a decrease in crossovers near subtelomeres, as well as increased average crossover distance to telomeres in infertile men. As telomere-guided mechanisms are speculated to play a role in crossover formation in subtelomeres, future studies linking crossover distribution with telomere integrity and sperm aneuploidy may provide new insight into the mechanisms underlying male infertility.
机译:在减数分裂期间,同源染色体配对以促进沿着染色体的交换位点处的DNA交换。严格控制交叉形成的频率和分布,以确保减数分裂的适当进展。我们的研究小组和其他研究小组使用免疫荧光技术研究了不育男性精子细胞中的减数分裂蛋白,表明与可育男性相比,该人群的交配频率降低。人们认为交换次数不足会促进染色体错集,在这种情况下,故障细胞可能会面临减数分裂停滞或促进非整倍性精子的产生。模型生物中越来越多的证据表明,交叉的分布对于正确的染色体分离也可能很重要。在正常男性中,在着丝粒和端粒附近很少出现交叉现象,而在亚端粒区域则很常见。我们的研究旨在表征非阻塞性(NOA)和阻塞性无精子症(OA)的不育男性沿染色体13、18和21的交叉分布特征。在我们的研究中,16名NOA男性中有8名和21名OA男性中有5名显示减少与控制可育男性相比,交叉频率更高。与对照相比,在所研究的至少一个染色体臂上,有7名NOA男子和9名OA男子表现出改变的交叉分布。我们发现,尽管NOA和OA男性均表现出改变的分频分布,但与OA男性相比,NOA男性可能面临更高的分频频率和分布改变的风险。我们的数据还表明,不育男性在正常受其抑制的区域,特别是着丝粒和端粒附近,跨界形成增加。最后,我们证明了在不育男性中近端粒的交换减少,以及到端粒的平均交换距离增加。由于端粒引导的机制被认为在亚端粒的交叉形成中起作用,因此将交叉分布与端粒完整性和精子非整倍性联系起来的未来研究可能会为男性不育的潜在机制提供新的见解。

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