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Coronavirus mRNA synthesis involves fusion of non-contiguous sequences
The EMBO Journal
|January 1, 1983
Summary
The mouse hepatitis virus (MHV) creates genomic RNA and subgenomic messenger RNAs (mRNAs) in the host cell cytoplasm. A unique polymerase jumping mechanism fuses non-contiguous leader and body sequences to form these mRNAs.
Area of Science:
- Virology
- Molecular Biology
- Genetics
Background:
- Coronaviruses, such as mouse hepatitis virus (MHV), possess a positive-stranded RNA genome.
- Viral RNA synthesis, including genomic and subgenomic messenger RNAs (mRNAs), occurs within the host cell's cytoplasm.
- The structure of MHV mRNAs involves leader and body sequences that are not adjacent on the viral genome.
Purpose of the Study:
- To elucidate the mechanism of subgenomic mRNA formation in MHV-infected cells.
- To investigate the process by which non-contiguous RNA sequences are joined during viral RNA synthesis.
Main Methods:
- Analysis of viral RNA synthesis in MHV-infected host cells.
- Characterization of the structure of genomic and subgenomic RNAs.
- Investigating the role of viral polymerase in RNA ligation.
Main Results:
- MHV genomic RNA and six subgenomic mRNAs are synthesized in the host cell cytoplasm.
- MHV mRNAs consist of leader and body sequences that are non-contiguous on the genome.
- RNA fusion appears to be mediated by a specific 'polymerase jumping' event.
Conclusions:
- The synthesis of MHV subgenomic mRNAs involves a novel mechanism of RNA ligation.
- The 'polymerase jumping' event is crucial for fusing non-contiguous RNA sequences, enabling the formation of functional mRNAs.