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Characterization of Plasma Extrachromosomal Circular DNA in Gouty Arthritis

Objective: 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. Methods: The Circle-Seq app...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019587/
https://www.ncbi.nlm.nih.gov/pubmed/35464862
http://dx.doi.org/10.3389/fgene.2022.859513
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author 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
author_facet 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
author_sort Pang, Jingyuan
collection PubMed
description Objective: 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. Methods: 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. Results: 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. Conclusion: Our discovery reveals the novel potential biological roles of plasma eccDNAs in gouty arthritis.
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spelling pubmed-90195872022-04-21 Characterization of Plasma Extrachromosomal Circular DNA in Gouty Arthritis 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 Front Genet Genetics Objective: 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. Methods: 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. Results: 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. Conclusion: Our discovery reveals the novel potential biological roles of plasma eccDNAs in gouty arthritis. Frontiers Media S.A. 2022-04-06 /pmc/articles/PMC9019587/ /pubmed/35464862 http://dx.doi.org/10.3389/fgene.2022.859513 Text en Copyright © 2022 Pang, Pan, Lin, Li, Yuan, Han, Ji, Li, Wang, Chu, Wu, Fan, Du and Ji. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
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
Characterization of Plasma Extrachromosomal Circular DNA in Gouty Arthritis
title Characterization of Plasma Extrachromosomal Circular DNA in Gouty Arthritis
title_full Characterization of Plasma Extrachromosomal Circular DNA in Gouty Arthritis
title_fullStr Characterization of Plasma Extrachromosomal Circular DNA in Gouty Arthritis
title_full_unstemmed Characterization of Plasma Extrachromosomal Circular DNA in Gouty Arthritis
title_short Characterization of Plasma Extrachromosomal Circular DNA in Gouty Arthritis
title_sort characterization of plasma extrachromosomal circular dna in gouty arthritis
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019587/
https://www.ncbi.nlm.nih.gov/pubmed/35464862
http://dx.doi.org/10.3389/fgene.2022.859513
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