Department of High Altitude Disease, College of High Altitude Military Medicine, Third Military Medical University, Chongqing, 400038, China.
J Assist Reprod Genet. 2011 Sep;28(10):951-6. doi: 10.1007/s10815-011-9620-y. Epub 2011 Sep 10.
Mitochondria are factories for energy production and genetic alterations in mtDNA will directly impact OXPHOS function. The copy number of mtDNA (i.e., the number of mtDNA per spermatozoon) is one of the major mitochondrial genetic features. Besides mtDNA copy number, the change of either mtDNA or nDNA integrity is another important factor causing asthenospermia, or poor sperm motility in infertile men. In this study, we investigated the mtDNA copy number and the integrities of mtDNA and nDNA respectively in semen samples from different donors at 5,300 m altitudes.
Total DNA was extracted from semen samples from donors in two different altitudes. Quantitative PCR was performed to evaluate the mtDNA copy number. PCR amplification was used to examine the integrity of sperm mtDNA. Flow cytometry was carried out to investigate sperm nDNA integrity. All data were analyzed to show the statistical significance.
Sperm mtDNA copy number for those living at high altitude (5,300 m) for one month was significantly higher (P < 0.05) than for those at the lower altitude (1,400 m) or in donors who had been living at the 5,300 m altitude for 1 year. In addition, sperm mtDNA copy numbers were remarkably decreased (P < 0.05) in those who had lived at the greater altitude for 1 year compared to those who had lived there for one month. The ratio of nDNA integrity among the 10,000 sperms at high altitude for one month was significantly lower (P < 0.05) than that at the lower altitude (1,400 m) or at 5,300 m for 1 year, and the ratio of nDNA integrity sperms at high altitude for 1 year was increased, and higher than that for at the lower altitude (P < 0.05).
High altitude can alter the mtDNA copy number and nDNA integrity in the sperms.
线粒体是能量产生的工厂,mtDNA 的遗传改变将直接影响 OXPHOS 功能。mtDNA 的拷贝数(即每个精子中的 mtDNA 数量)是线粒体遗传的主要特征之一。除了 mtDNA 拷贝数之外,mtDNA 或 nDNA 完整性的变化也是导致不育男性精子活力差或弱精症的另一个重要因素。在这项研究中,我们分别研究了来自不同供体在 5300 米海拔高度的精液样本中的 mtDNA 拷贝数以及 mtDNA 和 nDNA 的完整性。
从两个不同海拔高度的供体的精液样本中提取总 DNA。通过定量 PCR 评估 mtDNA 拷贝数。PCR 扩增用于检查精子 mtDNA 的完整性。通过流式细胞术检测精子 nDNA 完整性。分析所有数据以显示统计学意义。
在高海拔(5300 米)生活一个月的精子 mtDNA 拷贝数明显高于低海拔(1400 米)或在 5300 米海拔生活一年的供体(P<0.05)。此外,在高海拔生活一年的精子 mtDNA 拷贝数明显低于生活一个月的精子(P<0.05)。在高海拔生活一个月的 10000 个精子中,nDNA 完整性的比例明显低于低海拔(1400 米)或在 5300 米海拔生活一年的精子(P<0.05),而在高海拔生活一年的精子中 nDNA 完整性的比例增加,并且高于低海拔的精子(P<0.05)。
高海拔会改变精子中的 mtDNA 拷贝数和 nDNA 完整性。