Expression Profile and Function Analysis of Long Non-coding RNAs in the Infection of Coxsackievirus B3

被引:11
|
作者
Tong, Lei [1 ]
Qiu, Ye [2 ]
Wang, Hui [1 ]
Qu, Yunyue [1 ]
Zhao, Yuanbo [2 ]
Lin, Lexun [1 ]
Wang, Yan [3 ]
Xu, Weizhen [1 ]
Zhao, Wenran [3 ]
He, Hongyan [2 ]
Zhao, Guangze [4 ]
Zhang, Mary H. [4 ]
Yang, Decheng [4 ]
Ge, Xingyi [2 ]
Zhong, Zhaohua [1 ]
机构
[1] Harbin Med Univ, Dept Microbiol, Harbin 150081, Heilongjiang, Peoples R China
[2] Hunan Univ, Coll Biol, Changsha 410012, Hunan, Peoples R China
[3] Harbin Med Univ, Dept Cell Biol, Harbin 150081, Heilongjiang, Peoples R China
[4] Univ British Columbia, Dept Pathol & Lab Med, Vancouver, BC V6Z 1Y6, Canada
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Coxsackievirus B3 (CVB3); lncRNA-mRNA correlation network; Long non-coding RNA (lncRNA); XLOC-001188; NFAT5; ENHANCER RNAS; IDENTIFICATION; REPLICATION; BIOSYNTHESIS; MYOCARDITIS; APOPTOSIS; BIOLOGY; ROLES; PTEN;
D O I
10.1007/s12250-019-00152-x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The roles of lncRNAs in the infection of enteroviruses have been barely demonstrated. In this study, we used coxsackievirus B3 (CVB3), a typical enterovirus, as a model to investigate the expression profiles and functional roles of lncRNAs in enterovirus infection. We profiled lncRNAs and mRNA expression in CVB3-infected HeLa cells by lncRNA-mRNA integrated microarrays. As a result, 700 differentially expressed lncRNAs (431 up-regulated and 269 down-regulated) and 665 differentially expressed mRNAs (299 up-regulated and 366 down-regulated) were identified in CVB3 infection. Then we performed lncRNA-mRNA integrated pathway analysis to identify potential functional impacts of the differentially expressed mRNAs, in which lncRNA-mRNA correlation network was built. According to lncRNA-mRNA correlation, we found that XLOC-001188, an lncRNA down-regulated in CVB3 infection, was negatively correlated with NFAT5 mRNA, an anti-CVB3 gene reported previously. This interaction was supported by qPCR detection following siRNA-mediated knockdown of XLOC-001188, which showed an increase of NFAT5 mRNA and a reduction of CVB3 genomic RNA. In addition, we observed that four most significantly altered lncRNAs, SNHG11, RP11-145F16.2, RP11-1023L17.1 and RP11-1021N1.2 share several common correlated genes critical for CVB3 infection, such as BRE and IRF2BP1. In all, our studies reveal the alteration of lncRNA expression in CVB3 infection and its potential influence on CVB3 replication, providing useful information for future studies of enterovirus infection.
引用
收藏
页码:618 / 630
页数:13
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