Department of Andrology, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China.
National Clinical Research Center for Chinese Medicine Acupuncture and Moxibustion, Tianjin, China.
J Assist Reprod Genet. 2024 Oct;41(10):2795-2805. doi: 10.1007/s10815-024-03236-0. Epub 2024 Aug 27.
The aim of the current study was to investigate the mtDNA methylation levels and mtDNA copy numbers in the sperm of patients with asthenozoospermia and compare them to those observed in controls with normozoospermia.
Pyrosequencing analysis of the methylation levels of the mitochondrial D-loop and MT-CO1/chr1:631,907-632083/chrX:26,471,887-126,472,063 (hereinafter referred to as "MT-CO1-AVG") region and quantitative PCR analysis of the mtDNA copy number were performed on sperm from 30 patients with asthenozoospermia and 30 controls with normozoospermia.
Compared with those of controls with normozoospermia, the methylation levels of D-loop and MT-CO1-AVG regions and mtDNA copy number were significantly higher in patients with asthenozoospermia. The methylation level of the D-loop region in patients with asthenozoospermia and controls with normozoospermia and that of MT-CO1-AVG region in patients with asthenozoospermia showed a decreasing tendency with increasing total sperm motility. A significant inverse correlation between the mtDNA copy number and total sperm motility was observed in patients with asthenozoospermia but not in controls with normozoospermia. In patients with asthenozoospermia, but not in controls with normozoospermia, we observed a significant inverse correlation between D-loop methylation levels and mtDNA copy number, while no significant correlation was observed between MT-CO1-AVG methylation levels and mtDNA copy number.
These results reveal the occurrence of mtDNA methylation in human sperm and altered D-loop and MT-CO1-AVG methylation levels in patients with asthenozoospermia. Additional research is needed to determine the function of these features in the etiology and course of asthenozoospermia.
本研究旨在探讨弱精子症患者精子中线粒体 DNA(mtDNA)的甲基化水平和 mtDNA 拷贝数,并与正常精子对照进行比较。
采用焦磷酸测序分析线粒体 D 环和 MT-CO1/chr1:631,907-632083/chrX:26,471,887-126,472,063(以下简称“MT-CO1-AVG”)区域的甲基化水平,以及实时定量 PCR 分析 mtDNA 拷贝数,对 30 例弱精子症患者和 30 例正常精子对照者的精子进行检测。
与正常精子对照者相比,弱精子症患者的 D 环和 MT-CO1-AVG 区域的甲基化水平以及 mtDNA 拷贝数显著升高。弱精子症患者的 D 环区域和 MT-CO1-AVG 区域的甲基化水平与总精子活力呈逐渐下降的趋势。弱精子症患者 mtDNA 拷贝数与总精子活力呈显著负相关,但正常精子对照者则无此相关性。在弱精子症患者中,我们观察到 D 环甲基化水平与 mtDNA 拷贝数呈显著负相关,但在正常精子对照者中则无此相关性;而 MT-CO1-AVG 甲基化水平与 mtDNA 拷贝数之间无显著相关性。
这些结果揭示了人类精子中线粒体 DNA 甲基化的发生以及弱精子症患者 D 环和 MT-CO1-AVG 甲基化水平的改变。需要进一步的研究来确定这些特征在弱精子症的病因和病程中的作用。