Cap snatching of yeast L-A double-stranded RNA virus can operate in Trans and requires viral polymerase actively engaging in transcription

Eukaryotic mRNA bears a cap structure (m 7GpppX-) at the 5′ terminus crucial for efficient translation and stability. The yeast L-A double-stranded RNA virus furnishes its mRNA with this structure by a novel cap-snatching mechanism in which the virus transfers an m 7Gp moiety from host mRNA to the diphosphorylated 5′ terminus of the viral transcript, thus forming on it an authentic cap structure (referred to as cap0) in the budding yeast. This capping reaction is essential for efficient viral expression. His-154 of the capsid protein Gag is involved in the cap transfer. Here we show that the virus can utilize an externally added viral transcript as acceptor in the capping reaction. The acceptor needs to be 5′ diphosphorylated, consistent with the fact that the viral transcript bears diphosphate at the 5′ terminus. A 5′ triphosphorylated or monophosphorylated transcript does not function as acceptor. N7 methylation at the 5′ cap guanine of mRNA is essential for cap donor activity. We also demonstrate that the capping reaction requires the viral polymerase actively engaging in transcription. Because the cap-snatching site of Gag is located at the cytoplasmic surface of the virion, whereas Pol is confined inside the virion, the result indicates coordination between the cap-snatching and polymerization sites. This will allow L-A virus to efficiently produce capsid proteins to form new virions when Pol is actively engaging in transcription. The coordination may also minimize the risk of accidental capping of nonviral RNA when Pol is dormant. © 2012 by The American Society for Biochemistry and Molecular Biology, Inc.This work was supported by Grant BFU2010-15768 from the Spanish Ministry of Education and Science and by Fundación Ramón Areces.Peer Reviewe