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痛风性关节炎患者血浆染色体外环状DNA的特征分析

Characterization of Plasma Extrachromosomal Circular DNA in Gouty Arthritis.

作者信息

Pang Jingyuan, Pan Xiaoguang, Lin Ling, Li Lei, Yuan Shuai, Han Peng, Ji Xiaopeng, Li Hailong, Wang Can, Chu Zhaobin, Wu Haoru, Fan Guangyi, Du Xiao, Ji Aichang

机构信息

Medical School, Shandong University of Traditional Chinese Medicine, Jinan, China.

Lars Bolund Institute of Regenerative Medicine, Qingdao-Europe Advanced Institute for Life Sciences, BGI-Qingdao, Qingdao, China.

出版信息

Front Genet. 2022 Apr 6;13:859513. doi: 10.3389/fgene.2022.859513. eCollection 2022.

Abstract

Extrachromosomal circular DNA elements (eccDNAs) are known for their broad existence in cells and plasma, which may potentially play important roles in many biological processes. Our aim was to identify potentially functional or marked eccDNAs in gout patients. The Circle-Seq approach was applied for eccDNA detection from plasma in acute gout patients and healthy controls. Further analysis was performed on the distribution of genomic elements and eccDNA gene annotations in two groups. We detected 57,216 and 109,683 eccDNAs from the acute gout and healthy control plasma, respectively. EccDNAs were mapped to the reference genome to identify diverse classes of genomic elements and there was no significant difference of eccDNAs on genomic element annotation between gout and control group. A total of 256 eccDNA-associated genes were detected as gout unique eccDNA genes, including COL1A1 and EPB42, which potentially contribute to hyperuricemia and gout, and a couple of genes involved in inflammation or immune response. Enrichment analysis showed that these eccDNA genes were highly correlated with defense response, stress response, and immune and inflammatory responses, including T cell receptor signaling pathway, Fc epsilon RI signaling pathway, and JAK-STAT signaling pathway. Our discovery reveals the novel potential biological roles of plasma eccDNAs in gouty arthritis.

摘要

染色体外环状DNA元件(eccDNA)因其在细胞和血浆中广泛存在而闻名,它们可能在许多生物学过程中发挥重要作用。我们的目的是鉴定痛风患者中潜在具有功能或有标记的eccDNA。采用Circle-Seq方法从急性痛风患者和健康对照者的血浆中检测eccDNA。对两组中基因组元件的分布和eccDNA基因注释进行了进一步分析。我们分别从急性痛风患者和健康对照者的血浆中检测到57216个和109683个eccDNA。将eccDNA映射到参考基因组以鉴定不同类别的基因组元件,痛风组和对照组之间在基因组元件注释上的eccDNA没有显著差异。共检测到256个与eccDNA相关的基因作为痛风独特的eccDNA基因,包括COL1A1和EPB42,它们可能导致高尿酸血症和痛风,以及一些参与炎症或免疫反应的基因。富集分析表明,这些eccDNA基因与防御反应、应激反应以及免疫和炎症反应高度相关,包括T细胞受体信号通路、FcεRI信号通路和JAK-STAT信号通路。我们的发现揭示了血浆eccDNA在痛风性关节炎中的新的潜在生物学作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cdf/9019587/1cc271d913fb/fgene-13-859513-g001.jpg

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