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Bacterial Artificial Chromosomes: A Functional Genomics Tool for the Study of Positive-strand RNA Viruses
Published on: December 29, 2015
Coronavirus Replication: Genomes, Subgenomic RNAs, and Defective Viral Genomes
Rory Williams1,2, Jack Hales2, William Collier2
1Centre for Health and Life Sciences, Coventry University, Coventry CV1 2UD, UK.
Abstract:
With the emergence of the SARS-CoV-2 pandemic the process of coronavirus replication has been under increasing scrutiny. During the replication of their genomic RNA, coronaviruses produce a range of other RNAs in addition to the negative-sense replicative intermediates of the genome, which includes a set of subgenomic RNAs. These subgenomic RNAs are nested within the sequence of the complete genome and can be both replicated further and act as templates for protein production. Alongside these functional products of discontinuous replication, coronaviruses produce defective viral genomes that can potentially impact both the virus and infected host cells. These interactions can arise from the ability of these defective viral genomes to impact the production of new infectious virions, through either competition with the wild-type genome for replication or by stimulating an antiviral response. Examining the behaviour of defective viral genomes can also help to elucidate the functional elements of the genome involved in the processes of replication and packaging. This review covers the process of intracellular replication by coronaviruses describing the mechanisms by which the different RNA species are produced. Of particular focus are factors involved in discontinuous replication that produces defective viral genomes, and the behaviour of coronavirus defective viral genomes.
Insights
Coronaviruses produce various RNA types during replication, including defective viral genomes. Studying these defective genomes reveals insights into viral replication and host interactions.
Area of Science:
- Virology
- Molecular Biology
- Genetics
Background:
- The SARS-CoV-2 pandemic heightened interest in coronavirus replication mechanisms.
- Coronaviruses generate diverse RNA species, including subgenomic RNAs and defective viral genomes (DVGs), during replication.
- DVGs can influence viral production and host antiviral responses.
Purpose of the Study:
- To review the intracellular replication process of coronaviruses.
- To detail the mechanisms of RNA species production, focusing on discontinuous replication.
- To examine the behavior and implications of coronavirus defective viral genomes.
Main Methods:
- Review of existing literature on coronavirus RNA replication.
- Analysis of mechanisms underlying discontinuous RNA synthesis.
- Examination of the role and impact of defective viral genomes.
Main Results:
- Coronaviruses employ discontinuous replication to produce subgenomic RNAs and DVGs.
- DVGs can compete with wild-type genomes, affecting virion production.
- DVGs may trigger antiviral responses in host cells.
Conclusions:
- Understanding DVG production and behavior is crucial for comprehending coronavirus replication.
- DVGs offer insights into essential genomic elements for replication and packaging.
- Further research into DVGs can inform antiviral strategies.
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