Tian Meiping, Bao Huaqiong, Martin Francis L, Zhang Jie, Liu Liangpo, Huang Qingyu, Shen Heqing
Key Lab of Urban Environment and Health, Institute of Urban Environment, Chinese Academy of Sciences, Xiamen, China.
Chongqing Key Laboratory of Birth Defects and Reproductive Health, Affiliated Hospital of Chongqing Institute for Population and Family Planning, Chongqing, China.
Biol Reprod. 2014 Oct;91(4):101. doi: 10.1095/biolreprod.114.122465. Epub 2014 Sep 10.
Whether there is a relationship between quality, DNA methylation, and mitochondrial DNA (mtDNA) copy number in human-derived sperm specimens is unknown. A cohort (n = 118) of male partners of couples who were undergoing fertility assessment because of an idiopathic inability to conceive were recruited. Sperm motility parameters were determined by computer-aided sperm analysis (CASA), while sperm quality was assessed using World Health Organization criteria, mtDNA copy number was measured by real-time PCR, and DNA methylation patterns were analyzed employing high-melting resolution PCR and bisulfite sequencing PCR. The mtDNA copy number negatively correlated with semen parameters, including sperm motility, concentration, morphology, progression, and motion characteristics (r for -0.19 to -0.54; P < 0.05 for all). As a surrogate marker for global DNA methylation, LINE-1 negatively correlated with sperm motility (r = -0.25; P = 0.009). Meanwhile, after adjustment for age, length of abstinence, smoking, and alcohol intake, there was a suggested association for increased LINE-1 methylation and mtDNA copy number tertiles versus sperm motility (odd ratios were 1.0, 2.6, and 4.7, and 1.0, 2.5, and 4.9, respectively). Altered mtDNA copy number and DNA methylation may serve as genetic and epigenetic markers to assess human sperm quality together with CASA parameters.
在人类精子样本中,质量、DNA甲基化和线粒体DNA(mtDNA)拷贝数之间是否存在关联尚不清楚。招募了一组(n = 118)因特发性不孕而接受生育评估的夫妇的男性伴侣。精子活力参数通过计算机辅助精子分析(CASA)测定,精子质量使用世界卫生组织标准进行评估,mtDNA拷贝数通过实时PCR测量,DNA甲基化模式采用高熔解分辨率PCR和亚硫酸氢盐测序PCR进行分析。mtDNA拷贝数与精液参数呈负相关,包括精子活力、浓度、形态、进展和运动特征(r为-0.19至-0.54;所有P < 0.05)。作为全球DNA甲基化的替代标志物,LINE-1与精子活力呈负相关(r = -0.25;P = 0.009)。同时,在调整年龄禁欲时间、吸烟和饮酒量后,提示LINE-1甲基化增加和mtDNA拷贝数三分位数与精子活力之间存在关联(优势比分别为1.0、2.6和4.7,以及1.0、2.5和4.9)。改变的mtDNA拷贝数和DNA甲基化可能与CASA参数一起作为评估人类精子质量的遗传和表观遗传标志物。