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  3. Coronavirus takeover of host cell translation and intracellular antiviral response: a molecular perspective.

Coronavirus takeover of host cell translation and intracellular antiviral response: a molecular perspective.

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DOI
10.48350/191476
Publisher DOI
10.1038/s44318-023-00019-8
PubMed ID
38200146
Abstract
Coronaviruses are a group of related RNA viruses that cause respiratory diseases in humans and animals. Understanding the mechanisms of translation regulation during coronaviral infections is critical for developing antiviral therapies and preventing viral spread. Translation of the viral single-stranded RNA genome in the host cell cytoplasm is an essential step in the life cycle of coronaviruses, which affects the cellular mRNA translation landscape in many ways. Here we discuss various viral strategies of translation control, including how members of the Betacoronavirus genus shut down host cell translation and suppress host innate immune functions, as well as the role of the viral non-structural protein 1 (Nsp1) in the process. We also outline the fate of viral RNA, considering stress response mechanisms triggered in infected cells, and describe how unique viral RNA features contribute to programmed ribosomal -1 frameshifting, RNA editing, and translation shutdown evasion.
Date Issued
2024-01
Publication Type
Article
Subject(s)
500 Science > 570 Life sciences; biology
500 Science > 540 Chemistry
Subjects
Coronaviruses SARS-CoV-2 Translation Translation regulation Viral protein synthesis
Language(s)
en
Author(s)
Karousis, Evangelos  
Departement für Chemie, Biochemie und Pharmazie (DCBP) Universität Bern  
Schubert, Katharina
Ban, Nenad
Additional Credits
Departement für Chemie, Biochemie und Pharmazie (DCBP) Universität Bern  
Multidisciplinary Center for Infectious Diseases (MCID)  
Journal
The EMBO journal
Publisher
EMBO Press
ISSN
1460-2075
Access(Rights)
open.access
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