Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6141372 | Virology | 2011 | 10 Pages |
Abstract
The requirements for alignment of capped leader sequences along the viral genome during influenza transcription initiation (cap-snatching) have long been an enigma. In this study, competition experiments using an in vitro transcription assay revealed that influenza virus transcriptase prefers leader sequences with base complementarity to the 3â²-ultimate residues of the viral template, 10 or 11 nt from the 5â² cap. Internal priming at the 3â²-penultimate residue, as well as prime-and-realign was observed. The nucleotide identity immediately 5â² of the base-pairing residues also affected cap donor usage. Application to the in vitro system of RNA molecules with increased base complementarity to the viral RNA template showed stronger reduction of globin RNA leader initiated influenza transcription compared to those with a single base-pairing possibility. Altogether the results indicated an optimal cap donor consensus sequence of 7mG-(N)7-8-(A/U/G)-(A/U)-AGC-3â².
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Authors
Christina Geerts-Dimitriadou, Mark P. Zwart, Rob Goldbach, Richard Kormelink,