State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, World Health Organization Collaborating Center for Eye Care and Vision, Guangzhou, China.
Guangdong Provincial Clinical Research Center for Ocular Diseases, Guangzhou, China.
Epigenetics. 2024 Dec;19(1):2348840. doi: 10.1080/15592294.2024.2348840. Epub 2024 May 8.
To explore the role of lncRNA mA methylation modification in aqueous humour (AH) of patients with pseudoexfoliation glaucoma (PXG). Patients with open-angle PXG under surgery from June 2021 to December 2021 were selected. Age- and gender-matched patients with age-related cataract (ARC) were chosen as control. Patients underwent detailed ophthalmic examinations. 0.05-0.1 ml AH were extracted during surgery for MeRIP-Seq and RNA-Seq. Joint analysis was used to screen lncRNAs with differential mA methylation modification and expression. Online software tools were used to draw lncRNA-miRNA-mRNA network (ceRNA). Expression of lncRNAs and mRNAs was confirmed using quantitative real-time PCR. A total of 4151 lncRNAs and 4386 associated mA methylation modified peaks were identified in the PXG group. Similarly, 2490 lncRNAs and 2595 associated mA methylation modified peaks were detected in the control. Compared to the ARC group, the PXG group had 234 hypermethylated and 402 hypomethylated mA peaks, with statistically significant differences (| Fold Change (FC) |≥2, < 0.05). Bioinformatic analysis revealed that these differentially methylated lncRNA enriched in extracellular matrix formation, tight adhesion, TGF- β signalling pathway, AMPK signalling pathway, and MAPK signalling pathway. Joint analysis identified 10 lncRNAs with differential mA methylation and expression simultaneously. Among them, the expression of ENST000000485383 and ROCK1 were confirmed downregulated in the PXG group by RT-qPCR. mA methylation modification may affect the expression of lncRNA and participate in the pathogenesis of PXG through the ceRNA network. ENST000000485383-hsa miR592-ROCK1 May be a potential target pathway for further investigation in PXG mA methylation.
探讨长链非编码 RNA mA 甲基化修饰在假性剥脱性青光眼(PXG)患者房水中的作用。选择 2021 年 6 月至 12 月手术的开角型 PXG 患者为研究对象,选择年龄和性别匹配的年龄相关性白内障(ARC)患者为对照组。所有患者均接受详细的眼科检查。手术过程中提取 0.05-0.1ml 房水,用于 MeRIP-Seq 和 RNA-Seq。联合分析筛选差异 mA 甲基化修饰和表达的 lncRNA。在线软件工具用于绘制 lncRNA-miRNA-mRNA 网络(ceRNA)。采用实时荧光定量 PCR 验证 lncRNA 和 mRNA 的表达。在 PXG 组中鉴定出 4151 个 lncRNA 和 4386 个相关的 mA 甲基化修饰峰,在对照组中鉴定出 2490 个 lncRNA 和 2595 个相关的 mA 甲基化修饰峰。与 ARC 组相比,PXG 组有 234 个超甲基化峰和 402 个低甲基化峰,差异有统计学意义(| Fold Change (FC) |≥2,<0.05)。生物信息学分析显示,这些差异甲基化的 lncRNA 富集在细胞外基质形成、紧密粘连、TGF-β信号通路、AMPK 信号通路和 MAPK 信号通路。联合分析鉴定出 10 个同时具有差异 mA 甲基化和表达的 lncRNA。其中,ENST000000485383 和 ROCK1 的表达在 PXG 组中通过 RT-qPCR 证实下调。mA 甲基化修饰可能通过 ceRNA 网络影响 lncRNA 的表达,参与 PXG 的发病机制。ENST000000485383-hsa-miR592-ROCK1 可能是 PXG mA 甲基化的潜在研究靶点通路。