Department of Medical Biology, Faculty of Medicine, Ondokuz Mayis University, Samsun, Turkey.
Department of Multidisciplinary Molecular Medicine, Health Sciences Institute, Ondokuz Mayis University, Samsun, Turkey.
Andrologia. 2021 Feb;53(1):e13827. doi: 10.1111/and.13827. Epub 2020 Oct 28.
To investigate the semiquantitative methylation alterations of MLH1 and MSH2 and the possible association among methylation of MLH1 and MSH2, sperm DNA fragmentation and sperm chromatin condensation in idiopathic oligoasthenoteratozoospermic men. Seventy-five idiopathic infertile men and 52 fertile and/or normozoospermic men were included in the study. SDF was analysed using the TUNEL assay in semen samples of 100 men. Promoter methylation of MLH1 and MSH2 genes was assessed by semiquantitative methylight analysis in semen samples of 39 and 40 men respectively. Sperm chromatin condensation was evaluated using aniline blue staining in 114 men. MLH1 promoter methylation was positively correlated with the percentage of aniline blue positive spermatozoa (r = 0.401, p = 0.0188). On the other hand, MSH2 promoter methylation was negatively correlated with sperm concentration and total sperm count (r = -0.421, p = 0.0068 and r = 0.4408, p = 0.009 respectively). The percentage of aniline blue positive spermatozoa in the control group was significantly lower than in the OAT group (p < 0.0001) and negatively correlated with total sperm count (r = -0.683, p < 0.0001), progressive sperm motility (r = -0.628, p < 0.0001), total motility (r = -0.639, p < 0.0001) and normal morphology (r = -0.668, p < 0.0001). Promoter methylation profile of MLH1 and MSH2 genes may play role on sperm DNA packaging and conventional semen parameters respectively.
探讨特发性少弱畸精子症患者精子 MLH1 和 MSH2 基因的半定量甲基化改变及其与精子 DNA 碎片、精子染色质凝聚的关系。
纳入 75 例特发性不孕男性和 52 例生育力正常或精子参数正常的男性。100 例男性的精液样本通过 TUNEL 法分析精子 DNA 碎片化(SDF),39 例和 40 例男性的精液样本通过半定量甲基化 LIGHT 分析评估 MLH1 和 MSH2 基因启动子甲基化,114 例男性的精子染色质凝聚通过苯胺蓝染色评估。
MLH1 启动子甲基化与苯胺蓝阳性精子百分比呈正相关(r=0.401,p=0.0188)。另一方面,MSH2 启动子甲基化与精子浓度和总精子计数呈负相关(r=-0.421,p=0.0068 和 r=-0.4408,p=0.009)。对照组的苯胺蓝阳性精子百分比明显低于 OAT 组(p<0.0001),与总精子计数(r=-0.683,p<0.0001)、前向运动精子百分比(r=-0.628,p<0.0001)、总运动精子百分比(r=-0.639,p<0.0001)和正常形态精子百分比(r=-0.668,p<0.0001)呈负相关。MLH1 和 MSH2 基因启动子甲基化谱可能分别影响精子 DNA 包装和常规精液参数。
特发性少弱畸精子症患者 MLH1 和 MSH2 基因的半定量甲基化改变可能与精子 DNA 碎片化、精子染色质凝聚及精子参数异常有关。