Cargando…
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...
Autores principales: | , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1784689319276969984 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9019587 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT pangjingyuan characterizationofplasmaextrachromosomalcirculardnaingoutyarthritis AT panxiaoguang characterizationofplasmaextrachromosomalcirculardnaingoutyarthritis AT linling characterizationofplasmaextrachromosomalcirculardnaingoutyarthritis AT lilei characterizationofplasmaextrachromosomalcirculardnaingoutyarthritis AT yuanshuai characterizationofplasmaextrachromosomalcirculardnaingoutyarthritis AT hanpeng characterizationofplasmaextrachromosomalcirculardnaingoutyarthritis AT jixiaopeng characterizationofplasmaextrachromosomalcirculardnaingoutyarthritis AT lihailong characterizationofplasmaextrachromosomalcirculardnaingoutyarthritis AT wangcan characterizationofplasmaextrachromosomalcirculardnaingoutyarthritis AT chuzhaobin characterizationofplasmaextrachromosomalcirculardnaingoutyarthritis AT wuhaoru characterizationofplasmaextrachromosomalcirculardnaingoutyarthritis AT fanguangyi characterizationofplasmaextrachromosomalcirculardnaingoutyarthritis AT duxiao characterizationofplasmaextrachromosomalcirculardnaingoutyarthritis AT jiaichang characterizationofplasmaextrachromosomalcirculardnaingoutyarthritis |