首页> 外文期刊>Human Reproduction >Mossman, J.A.a d , Slate, J.a , Birkhead, T.R.a , Moore, H.D.b , Pacey, A.A.c Mitochondrial haplotype does not influence sperm motility in a UK population of men
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Mossman, J.A.a d , Slate, J.a , Birkhead, T.R.a , Moore, H.D.b , Pacey, A.A.c Mitochondrial haplotype does not influence sperm motility in a UK population of men

机译:Mossman,J.A. a d,Slate,J.a,Birkhead,T.R.a,Moore,H.D.b,Pacey,A.c线粒体单倍型不会影响英国男性人群的精子活力。

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Background Sperm motility is regulated by mitochondrial enzymes that are partially encoded by mitochondrial DNA (mtDNA). MtDNA has therefore been suggested as a putative genetic marker of male fertility. However, recent studies in different populations have identified both significant and non-significant associations between mtDNA variation and sperm motility. Here, we tested whether mtDNA variation was associated with sperm motility in a large cohort of men from the UK, to test the robustness of previous studies and the reliability of mtDNA as a marker of poor sperm motility.Methods A total of 463 men attending for semen analysis as part of infertility investigations were recruited from a UK laboratory. Sperm motility was measured using both computer-assisted sperm analysis and traditional manual measurements. MtDNA haplogroup and haplotype were determined in 357 and 298 men, respectively, using single nucleotide polymorphism (SNP) markers throughout the mtDNA genome, and compared with sperm motility data. The linkage between the SNP markers, and possible associations between individual SNPs and motility, were also investigated. Results We found no statistical association between haplogroup or haplotype and sperm motility, regardless of how it was measured (P > 0.05 in all cases). Moreover, individual SNPs which were in linkage disequilibrium and dispersed across the mitochondrial genome, and therefore sensitive to mtDNA variation, were not predictive of sperm motility. Conclusions Mitochondrial haplotype is unlikely to be a reliable genetic marker of male factor infertility.
机译:背景技术精子的运动性由线粒体DNA(mtDNA)部分编码的线粒体酶调节。因此,MtDNA被认为是雄性育性的公认遗传标记。但是,最近在不同人群中进行的研究已经确定了mtDNA变异与精子活力之间的显着和非显着关联。在这里,我们测试了英国大量男性的mtDNA变异是否与精子活力有关,以检验以前的研究的稳健性以及mtDNA作为精子活力低下的指标的可靠性。方法共有463名男性参加精液分析是不孕症调查的一部分,是从英国实验室招募的。使用计算机辅助的精子分析和传统的手动测量来测量精子活力。使用整个mtDNA基因组中的单核苷酸多态性(SNP)标记分别确定了357名和298名男性的MtDNA单倍型和单倍型,并与精子活力数据进行了比较。还研究了SNP标记之间的联系,以及各个SNP与运动之间的可能联系。结果我们发现单倍型或单倍型与精子活力之间无统计学联系,无论如何测量(在所有情况下,P> 0.05)。此外,处于连锁不平衡状态并分散在线粒体基因组中的单个SNP,因此对mtDNA变异敏感,不能预测精子的运动能力。结论线粒体单倍型不太可能成为男性不育症的可靠遗传标记。

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