Abstract
Influenza A virus genome RNA segment 7 encodes three known mRNAs, two of which, M2 mRNA and M mRNA3, are derived by alternative splicing of the primary collinear mRNA transcript using alternative 5' splice sites. The function of M mRNA3 is currently unknown, therefore we attempted to determine whether it is essential for virus replication. Recombinant viruses unable to produce M mRNA3 and/or M2 mRNA were created by mutating the shared 3' splice site. Growth of the mutant viruses in M2-expressing MDCK cells was not significantly affected by the lack of M mRNA3. During the course of a wild-type virus infection, levels of M mRNA3 began to decrease while those of M2 mRNA increased, which may indicate a potential mechanism of alternative splicing control. These data suggest that neither M mRNA3 nor any potential protein product are essential for influenza virus replication in tissue culture.
| Original language | English |
|---|---|
| Pages (from-to) | 3097-3101 |
| Number of pages | 5 |
| Journal | Journal of General Virology |
| Volume | 89 |
| DOIs | |
| Publication status | Published - Dec 2008 |
Keywords
- ION-CHANNEL PROTEIN
- INFECTED-CELLS
- VIRION RNA
- GENERATION
- STABILITY
- SEGMENT-7
- SEQUENCES
- SITES
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