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Translational termination-reinitiation in RNA viruses
1Division of Virology, Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QP, UK. mlp34@cam.ac.uk
Biochemical Society Transactions
|December 2, 2010
Summary
Viruses use termination-dependent reinitiation to control protein expression from polycistronic mRNAs. This review explores how mRNA-rRNA interactions facilitate ribosomal reinitiation in various RNA viruses.
Area of Science:
- Virology
- Molecular Biology
- Genetics
Background:
- Viruses employ translational control on polycistronic mRNAs to regulate viral protein expression.
- Termination-dependent reinitiation is a key mechanism observed in both negative- and positive-strand RNA viruses.
- Dicistronic RNAs often feature overlapping stop and start codons for upstream and downstream open reading frames (ORFs).
Purpose of the Study:
- To review the mechanisms of termination-dependent reinitiation in RNA viruses.
- To highlight the role of mRNA-ribosomal RNA interactions in facilitating reinitiation.
- To discuss viral reinitiation strategies, including those independent of direct mRNA-rRNA interactions.
Main Methods:
- Literature review of viral translational control mechanisms.
- Analysis of specific viral RNA structures and sequences involved in reinitiation.
- Comparative study of reinitiation strategies across different RNA virus families.
Main Results:
- Termination-dependent reinitiation is a conserved viral strategy.
- mRNA-rRNA interactions are crucial for tethering ribosomal subunits, aiding reinitiation.
- Examples include influenza B and caliciviruses, showcasing specific sequence overlaps (e.g., UAAUG).
Conclusions:
- mRNA-rRNA interactions play a significant role in viral translational control.
- Understanding these mechanisms provides insights into viral replication and gene expression.
- Diverse strategies exist for viral reinitiation, with or without direct RNA-RNA contact.
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