IRES-dependent ribosome repositioning directs translation of a +1 overlapping ORF that enhances viral infection. Issue 22 (10th November 2018)

• Record Type: Journal Article
• Authors: Kerr, Craig H; Wang, Qing S; Moon, Kyung-Mee; Keatings, Kathleen; Allan, Douglas W; Foster, Leonard J; Jan, Eric
• Is Part Of: Nucleic acids research. Volume 46:Issue 22(2018)
• Page Start: 11952
• Page End: 11967
• Publication Date: 2018-11-10
• Subjects: Nucleic acids -- Periodicals; Molecular biology -- Periodicals; 572.805
• DOI: 10.1093/nar/gky1121
• Languages: English
• ISSNs: 0305-1048

Abstract

Abstract: RNA structures can interact with the ribosome to alter translational reading frame maintenance and promote recoding that result in alternative protein products. Here, we show that the internal ribosome entry site (IRES) from the dicistrovirus Cricket paralysis virus drives translation of the 0-frame viral polyprotein and an overlapping +1 open reading frame, called ORFx, via a novel mechanism whereby a subset of ribosomes recruited to the IRES bypasses 37 nucleotides downstream to resume translation at the +1-frame 13th non-AUG codon. A mutant of CrPV containing a stop codon in the +1 frame ORFx sequence, yet synonymous in the 0-frame, is attenuated compared to wild-type virus in a Drosophila infection model, indicating the importance of +1 ORFx expression in promoting viral pathogenesis. This work demonstrates a novel programmed IRES-mediated recoding strategy to increase viral coding capacity and impact virus infection, highlighting the diversity of RNA-driven translation initiation mechanisms in eukaryotes.