MLH1
MSH2
甲基化
DNA甲基化
生物
男科
男性不育
遗传学
DNA错配修复
不育
医学
基因
DNA修复
怀孕
基因表达
作者
Sezgin Güneş,Ashok Agarwal,Ralf Henkel,Asli Metin Mahmutoglu,Rakesh Sharma,Sandro C. Esteves,Abdulrahman Aljowair,D. Emirzeoglu,Abdullah Alkhani,Lucas Nogueira de Carvalho Pelegrini,Ahmad Joumah,Edmund Sabanegh
出处
期刊:Andrologia
[Wiley]
日期:2017-10-06
卷期号:50 (3): e12903-e12903
被引量:30
摘要
MLH1 and MSH2 are important genes for DNA mismatch repair and crossing over during meiosis and are implicated in male infertility. Therefore, the methylation patterns of the DNA mismatch repair genes MLH1 and MSH2 in oligozoospermic males were investigated. Ten oligozoospermic patients and 29 normozoospermic donors were analysed. Methylation profiles of the MLH1 and MSH2 promotors were analysed. In addition, sperm motility and seminal reactive oxygen species (ROS) were recorded. Receiver operating characteristic (ROC) analysis was conducted to determine the accuracy of the DNA methylation status of MLH1 and MSH2 to distinguish between oligozoospermic and normozoospermic men. In oligozoospermic men, MLH1 was significantly (p = .0013) more methylated compared to normozoospermic men. Additionally, there was a significant positive association (r = .384; p = .0159) between seminal ROS levels and MLH1 methylation. Contrary, no association between MSH2 methylation and oligozoospermia was found. ROC curve analysis for methylation status of MLH1 was significant (p = .0275) with an area under the curve of 61.1%, a sensitivity of 22.2% and a specificity of 100.0%. This pilot study indicates oligozoospermic patients have more methylation of MLH1 than normozoospermic patients. Whether hypermethylation of the MLH1 promoter plays a role in repairing relevant mismatches of sperm DNA strands in idiopathic oligozoospermia warrants further investigation.
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