感染柯萨奇病毒 B5 的 SH-SY5Y 细胞中差异表达的环状 RNA 的表达谱和 circRNA-miRNA-mRNA 调控网络

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY International Journal of Genomics Pub Date : 2022-10-10 eCollection Date: 2022-01-01 DOI:10.1155/2022/9298149
Jing Li, Heng Yang, Huaran Shi, Jihong Zhang, Wei Chen
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摘要

柯萨奇病毒 B5(CVB5)是手足口病(HFMD)的病原体,可导致神经系统并发症和死亡。循环 RNA(circRNA)已被证明在调节致病过程中发挥重要作用。然而,circRNA 在应对 CVB5 感染时的功能仍不清楚。我们的研究采用 RNA-seq 技术分析了感染或未感染 CVB5 的 SH-SY5Y 细胞中 circRNA 的表达谱。在SH-SY5Y细胞中表达的5665个circRNA中,发现163个circRNA有显著的差异表达。此外,基因本体(GO)和京都基因和基因组百科全书(KEGG)分析表明,在CVB5感染期间,差异表达的circRNA主要参与泛素介导的蛋白水解和信号通路。此外,我们还利用 RT-qPCR 验证了 RNA-seq 数据,并根据与宿主细胞先天免疫反应调控相关的两个 circRNA(如 hsa_circ_0008378 和 novel_circ_0014617)构建了 circRNA-miRNA-mRNA 相互作用网络。此外,我们还证实这两种 circRANs 能上调 IFN-I 信号通路中的关键因子,从而阻碍病毒复制。我们的数据提供了一个新的视角,有助于进一步了解病毒-宿主机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Expression Profiles of Differentially Expressed Circular RNAs and circRNA-miRNA-mRNA Regulatory Networks in SH-SY5Y Cells Infected with Coxsackievirus B5.

Coxsackievirus B5 (CVB5) is the causative agent of hand, foot, and mouth disease (HFMD) that can cause neurological complications and fatalities. Circular RNA (circRNA) has been shown to play an important role in regulating pathogenic processes. However, the functions of circRNA in response to CVB5 infection remain unclear. In our research, RNA-seq was employed to analyze the expression profiles of circRNAs in SH-SY5Y cells with or without CVB5 infection. Out of 5,665 circRNAs identified to be expressed in SH-SY5Y cells, 163 circRNAs were found to be differentially expressed significantly. Moreover, Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses showed that the differentially expressed circRNAs were mainly involved in ubiquitin-mediated proteolysis and signaling pathways during CVB5 infection. Additionally, RT-qPCR was used to validate the RNA-seq data, and a circRNA-miRNA-mRNA interaction network was constructed based on two circRNAs, such as hsa_circ_0008378 and novel_circ_0014617, which were associated with the regulation of innate immune response in host cells. Additionally, we confirmed the two circRANs up-regulated the key factors in the IFN-I signaling pathway, hampering viral replication. Our data provide a new perspective that facilitates further understanding of the virus-host mechanism.

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来源期刊
International Journal of Genomics
International Journal of Genomics BIOCHEMISTRY & MOLECULAR BIOLOGY-BIOTECHNOLOGY & APPLIED MICROBIOLOGY
CiteScore
5.40
自引率
0.00%
发文量
33
审稿时长
17 weeks
期刊介绍: International Journal of Genomics is a peer-reviewed, Open Access journal that publishes research articles as well as review articles in all areas of genome-scale analysis. Topics covered by the journal include, but are not limited to: bioinformatics, clinical genomics, disease genomics, epigenomics, evolutionary genomics, functional genomics, genome engineering, and synthetic genomics.
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