甲基化位点cg06972019调控琥珀酰化相关基因ENO1,抑制勃起功能障碍的发生。

IF 2.5 3区 生物学
Jian Wang, Siyuan Ye, Maoxiao Xu, Mengru Sun, Yang Lu, Zhenrong Piao, Fengmeng Teng, Maosen Zhang
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引用次数: 0

摘要

背景:本研究旨在探讨琥珀酰化相关基因表达与勃起功能障碍(ED)之间的因果关系。方法:通过查阅文献,鉴定出19个琥珀酰化相关基因,并与eQTLGen Consortium的顺式表达定量性状位点(cis-eQTL)数据进行交叉,最终筛选出16个具有顺式eqtl数据的基因。随后,我们从IEU OpenGWAS项目的223,805名欧洲男性参与者中下载了与勃起功能障碍(ED)相关的基因组数据,并进行了双样本孟德尔随机化(MR)分析。基于总结的孟德尔随机化(SMR)分析和ELISA检测进一步证实了ENO1基因表达与ED风险之间的统计学关联。通过中介分析探讨DNA甲基化在基因表达与ED之间的潜在调控作用。结果:通过MR分析,发现ENO1基因与ED之间存在显著的因果关系。结论:本研究通过孟德尔随机化和SMR分析揭示了ENO1基因在ED发生过程中的潜在因果关系,进一步验证了该基因表达与ED之间的关联,ENO1基因的过表达可能受甲基化位点cg06972019的调控。这些发现为ED的分子机制提供了新的见解,并可能为ED的早期诊断和靶向治疗提供新的生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The methylation site cg06972019 regulates the succinylation-related gene ENO1 to inhibit the occurrence of erectile dysfunction.

The methylation site cg06972019 regulates the succinylation-related gene ENO1 to inhibit the occurrence of erectile dysfunction.

The methylation site cg06972019 regulates the succinylation-related gene ENO1 to inhibit the occurrence of erectile dysfunction.

The methylation site cg06972019 regulates the succinylation-related gene ENO1 to inhibit the occurrence of erectile dysfunction.

Background: This study aims to explore the causal relationship between the expression of succinylation-related genes and erectile dysfunction (ED).

Method: Through a literature review, we identified 19 succinylation-related genes and intersected them with cis-expression Quantitative Trait Loci (cis-eQTL) data from the eQTLGen Consortium, ultimately selecting 16 genes with available cis-eQTL data. Subsequently, we downloaded genomic data related to erectile dysfunction (ED) from 223,805 European male participants in the IEU OpenGWAS project and performed a two-sample Mendelian Randomization (MR) analysis. Summary-based Mendelian Randomization (SMR) analysis and ELISA testing further confirmed the statistical association between ENO1 gene expression and ED risk. Mediation analysis was used to explore the potential regulatory role of DNA methylation in the relationship between gene expression and ED.

Result: Through MR analysis, a significant causal relationship between the ENO1 gene and ED was identified. The results indicated that the expression of the ENO1 gene has a significant causal effect on the risk of ED (OR: 1.2388, 95% CI: 1.0708-1.4332, p < 0.05). SMR analysis further confirmed the causal relationship between ENO1 gene expression and ED (SMR_p-value = 0.0040). Mediation analysis suggested that the methylation site cg06972019 may inhibit the occurrence of ED by regulating ENO1, with the mediation proportion accounting for 67.6% of the total effect (P = 0.0013). ELISA results showed that the serum ENO1 levels in ED patients were significantly higher than those in the healthy control group (p < 0.05), validating the potential role of ENO1 in ED.

Conclusion: This study revealed the potential causal relationship of the ENO1 gene in the development of ED through Mendelian Randomization and SMR analysis, further validating the association between gene expression and ED. The overexpression of the ENO1 gene may be regulated by the methylation site cg06972019. These findings provide new insights into the molecular mechanisms of ED and may offer new biomarkers for the early diagnosis and targeted treatment of ED.

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来源期刊
Hereditas
Hereditas Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.80
自引率
3.70%
发文量
0
期刊介绍: For almost a century, Hereditas has published original cutting-edge research and reviews. As the Official journal of the Mendelian Society of Lund, the journal welcomes research from across all areas of genetics and genomics. Topics of interest include human and medical genetics, animal and plant genetics, microbial genetics, agriculture and bioinformatics.
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