Human Cytomegalovirus Induced Aberrant Expression of Non-coding RNAs

Human cytomegalovirus (HCMV) is a β-herpesvirus whose genome consists of double stranded linear DNA. HCMV genome can generate non-coding RNAs (ncRNAs) through transcription in its host cells. Besides that, HCMV infection also changes the ncRNAs expression profile of the host cells. ncRNAs play a key...

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Published inFrontiers in microbiology Vol. 13; p. 918213
Main Authors Yu, Zhongjie, Wang, Jing, Nan, Fulong, Shi, Wenyi, Zhang, Xianjuan, Jiang, Shasha, Wang, Bin
Format Journal Article
LanguageEnglish
Published Frontiers Media S.A 13.06.2022
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Summary:Human cytomegalovirus (HCMV) is a β-herpesvirus whose genome consists of double stranded linear DNA. HCMV genome can generate non-coding RNAs (ncRNAs) through transcription in its host cells. Besides that, HCMV infection also changes the ncRNAs expression profile of the host cells. ncRNAs play a key role in maintaining the normal physiological activity of cells, and the disorder of ncRNAs expression has numerous adverse effects on cells. However, until now, the relationship between ncRNAs and HCMV-induced adverse effects are not summarized in detail. This review aims to give a systematic summary of the role of HCMV infection in ncRNAs expression while providing insights into the molecular mechanism of unnormal cellular events caused by ncRNAs disorder. ncRNAs disorder induced by HCMV infection is highly associated with cell proliferation, apoptosis, tumorigenesis, and immune regulation, as well as the development of cardiovascular diseases, and the potential role of biomarker. We summarize the studies on HCMV associated ncRNAs disorder and suggest innovative strategies for eliminating the adverse effects caused by HCMV infection.
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Edited by: Patricia Fitzgerald-Bocarsly, The State University of New Jersey, United States
This article was submitted to Virology, a section of the journal Frontiers in Microbiology
Reviewed by: Qiliang Cai, Fudan University, China; Benjamin Anthony Krishna, Lerner Research Institute, Cleveland Clinic, United States
ISSN:1664-302X
1664-302X
DOI:10.3389/fmicb.2022.918213