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• W2123378889 abstract "Nonsegmented negative-sense (nsNS) RNA viruses typically replicate within the host cell cytoplasm and do not have access to the host mRNA capping machinery. These viruses have evolved a unique mechanism for mRNA cap formation in that the guanylyltransferase transfers GDP rather than GMP onto the 5′ end of the RNA. Working with vesicular stomatitis virus (VSV), a prototype nsNS RNA virus, we now provide genetic and biochemical evidence that its mRNA cap methylase activities are also unique. Using recombinant VSV, we determined the function in mRNA cap methylation of a predicted binding site in the polymerase for the methyl donor, S -adenosyl- l -methionine. We found that amino acid substitutions to this site disrupted methylation at the guanine-N-7 (G-N-7) position or at both the G-N-7 and ribose-2′-O (2′-O) positions of the mRNA cap. These studies provide genetic evidence that the two methylase activities share an S -adenosyl- l -methionine-binding site and show that, in contrast to other cap methylation reactions, methylation of the G-N-7 position is not required for 2′-O methylation. These findings suggest that VSV evolved an unusual strategy of mRNA cap methylation that may be shared by other nsNS RNA viruses." @default.
• W2123378889 created "2016-06-24" @default.
• W2123378889 creator A5008176889 @default.
• W2123378889 creator A5013944987 @default.
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• W2123378889 date "2006-05-30" @default.
• W2123378889 modified "2023-10-14" @default.
• W2123378889 title "A unique strategy for mRNA cap methylation used by vesicular stomatitis virus" @default.
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• W2123378889 doi "https://doi.org/10.1073/pnas.0509821103" @default.
• W2123378889 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/1482520" @default.
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• W2123378889 hasPublicationYear "2006" @default.
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