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Abnormal Hypermethylation of the VDAC2 Promoter is a Potential Cause of Idiopathic Asthenospermia in Men

机译:VDAC2启动子的异常过度甲基化是男性特发性弱精子症的潜在原因

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摘要

This study aimed to explore the association between the methylation status of the VDAC2 gene promoter region and idiopathic asthenospermia (IAS). Twenty-five IAS patients and 27 fertile normozoospermia (NZ) were involved. GC-2spd cells were treated with different concentrations of 5-aza-2′-deoxycytidine (5-Aza-CdR) for 24 h and 48 h. qRT-PCR was conducted to reveal whether or not VDAC2 expression was regulated by methylated modification. A dual-luciferase activity detection was used to verify VDAC2 promoter activity in GC-2spd cells. Bisulphite genomic sequence was used to analyse DNA methylation of the VDAC2 promoter. The results showed that VDAC2 expression was significantly increased after treated with 5-Aza-CdR. A strong activity of the promoter (−2000 bp to +1000 bp) was detected by dual-luciferase activity detection (P < 0.05). The bisulphite genomic sequencing and correlation analysis showed that sperm motility was positively associated with the methylation pattern of uncomplete methylation and mild hypermethylation, and negatively related to the percentage of moderate methylation. In conclusion, high methylation of the VDAC2 promoter CpGs could be positively correlated with low sperm motility. Abnormal methylation of VDAC2 promoter may be a potential cause to idiopathic asthenospermia.
机译:这项研究旨在探讨VDAC2基因启动子区域的甲基化状态与特发性弱精子症(IAS)之间的关联。涉及25例IAS患者和27例可育正常精子症(NZ)。用不同浓度的5-氮杂-2'-脱氧胞苷(5-氮杂-CdR)处理GC-2spd细胞24 h和48 h。进行qRT-PCR以揭示VDAC2表达是否受甲基化修饰调控。使用双重萤光素酶活性检测来验证GC-2spd细胞中的VDAC2启动子活性。亚硫酸氢盐基因组序列用于分析VDAC2启动子的DNA甲基化。结果表明,用5-Aza-CdR处理后,VDAC2表达显着增加。通过双萤光素酶活性检测(P the <0.05),检测到该启动子具有很强的活性(-2000 bp至+1000 bp)。亚硫酸氢盐基因组测序和相关分析表明,精子活力与甲基化不完全和轻度甲基化程度呈正相关,与中等甲基化百分比呈负相关。总之,VDAC2启动子CpG的高甲基化可能与低精子活动性正相关。 VDAC2启动子的甲基化异常可能是特发性弱精子症的潜在原因。

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