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全基因组鉴定与类风湿关节炎相关的 RNA 修饰相关单核苷酸多态性。

Genome-wide identification of RNA modification-related single nucleotide polymorphisms associated with rheumatoid arthritis.

机构信息

Center for Genetic Epidemiology and Genomics, Department of Epidemiology, School of Public Health, Medical College of Soochow University, 199 Renai Road, Suzhou, Jiangsu, 215123, People's Republic of China.

Jiangsu Key Laboratory of Preventive and Translational Medicine for Geriatric Diseases, School of Public Health, Medical College of Soochow University, Suzhou, China.

出版信息

BMC Genomics. 2023 Mar 27;24(1):153. doi: 10.1186/s12864-023-09227-2.

Abstract

BACKGROUND

RNA modification plays important roles in many biological processes, such as gene expression control. The aim of this study was to identify single nucleotide polymorphisms related to RNA modification (RNAm-SNPs) for rheumatoid arthritis (RA) as putative functional variants.

METHODS

We examined the association of RNAm-SNPs with RA in summary data from a genome-wide association study of 19,234 RA cases and 61,565 controls. We performed eQTL and pQTL analyses for the RNAm-SNPs to find associated gene expression and protein levels. Furthermore, we examined the associations of gene expression and circulating protein levels with RA using two-sample Mendelian randomization analysis methods.

RESULTS

A total of 160 RNAm-SNPs related to mA, mA, A-to-I, mG, mC, mU and mAm modifications were identified to be significantly associated with RA. These RNAm-SNPs were located in 62 protein-coding genes, which were significantly enriched in immune-related pathways. RNAm-SNPs in important RA susceptibility genes, such as PADI2, SPRED2, PLCL2, HLA-A, HLA-B, HLA-DRB1, HLA-DPB1, TRAF1 and TXNDC11, were identified. Most of these RNAm-SNPs showed eQTL effects, and the expression levels of 26 of the modifiable genes (e.g., PADI2, TRAF1, HLA-A, HLA-DRB1, HLA-DPB1 and HLA-B) in blood cells were associated with RA. Circulating protein levels, such as CFB, GZMA, HLA-DQA2, IL21, LRPAP1 and TFF3, were affected by RNAm-SNPs and were associated with RA.

CONCLUSION

The present study identified RNAm-SNPs in the reported RA susceptibility genes and suggested that RNAm-SNPs may affect RA risk by affecting the expression levels of corresponding genes and proteins.

摘要

背景

RNA 修饰在许多生物过程中发挥重要作用,例如基因表达调控。本研究旨在鉴定与 RNA 修饰(RNAm-SNPs)相关的单核苷酸多态性,作为潜在的功能变异,以用于类风湿关节炎(RA)。

方法

我们在对 19234 例 RA 病例和 61565 例对照的全基因组关联研究的汇总数据中,检测了 RNAm-SNPs 与 RA 的关联。我们对 RNAm-SNPs 进行了 eQTL 和 pQTL 分析,以寻找相关的基因表达和蛋白质水平。此外,我们使用两样本 Mendelian 随机化分析方法,检测了基因表达和循环蛋白水平与 RA 的关联。

结果

共鉴定出 160 个与 mA、m6A、A-to-I、mG、mC、mU 和 mAm 修饰相关的 RNAm-SNPs,这些 SNPs 与 RA 显著相关。这些 RNAm-SNPs 位于 62 个编码蛋白的基因中,这些基因显著富集在免疫相关通路中。在重要的 RA 易感基因(如 PADI2、SPRED2、PLCL2、HLA-A、HLA-B、HLA-DRB1、HLA-DPB1、TRAF1 和 TXNDC11)中发现了 RNAm-SNPs。这些 RNAm-SNPs 大多数具有 eQTL 效应,并且血细胞中 26 个可修饰基因(如 PADI2、TRAF1、HLA-A、HLA-DRB1、HLA-DPB1 和 HLA-B)的表达水平与 RA 相关。CFB、GZMA、HLA-DQA2、IL21、LRPAP1 和 TFF3 等循环蛋白水平受 RNAm-SNPs 影响并与 RA 相关。

结论

本研究鉴定了报告的 RA 易感基因中的 RNAm-SNPs,并表明 RNAm-SNPs 可能通过影响相应基因和蛋白质的表达水平来影响 RA 风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18df/10045113/59b055ac3b54/12864_2023_9227_Fig1_HTML.jpg

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