Genome-Wide Search for Competing Endogenous RNAs Responsible for the Effects Induced by Ebola Virus Replication and Transcription Using a trVLP System.
Zhong-Yi Wang, Zhen-Dong Guo, Jia-Ming Li, Zong-Zheng Zhao, Ying-Ying Fu, Chun-Mao Zhang, Yi Zhang, Li-Na Liu, Jun Qian, Lin-Na Liu
Author Information
Zhong-Yi Wang: Academy of Military Medical Sciences, Beijing, China.
Zhen-Dong Guo: Academy of Military Medical Sciences, Beijing, China.
Jia-Ming Li: Key Laboratory of Jilin Province for Zoonosis Prevention and Control, Changchun, China.
Zong-Zheng Zhao: Academy of Military Medical Sciences, Beijing, China.
Ying-Ying Fu: Academy of Military Medical Sciences, Beijing, China.
Chun-Mao Zhang: Academy of Military Medical Sciences, Beijing, China.
Yi Zhang: Academy of Military Medical Sciences, Beijing, China.
Li-Na Liu: Key Laboratory of Jilin Province for Zoonosis Prevention and Control, Changchun, China.
Jun Qian: Academy of Military Medical Sciences, Beijing, China.
Lin-Na Liu: Academy of Military Medical Sciences, Beijing, China.
Understanding how infected cells respond to Ebola virus (EBOV) and how this response changes during the process of viral replication and transcription are very important for establishing effective antiviral strategies. In this study, we conducted a genome-wide screen to identify long non-coding RNAs (lncRNAs), circular RNAs (circRNAs), micro RNAs (miRNAs), and mRNAs differentially expressed during replication and transcription using a tetracistronic transcription and replication-competent virus-like particle (trVLP) system that models the life cycle of EBOV in 293T cells. To characterize the expression patterns of these differentially expressed RNAs, we performed a series cluster analysis, and up- or down-regulated genes were selected to establish a gene co-expression network. Competing endogenous RNA (ceRNA) networks based on the RNAs responsible for the effects induced by EBOV replication and transcription in human cells, including circRNAs, lncRNAs, miRNAs, and mRNAs, were constructed for the first time. Based on these networks, the interaction details of circRNA-chr19 were explored. Our results demonstrated that circRNA-chr19 targeting miR-30b-3p regulated CLDN18 expression by functioning as a ceRNA. These findings may have important implications for further studies of the mechanisms of EBOV replication and transcription. These RNAs potentially have important functions and may be promising targets for EBOV therapy.
