Analysis of a 3′-translation enhancer in a tombusvirus: A dynamic model for RNA–RNA interactions of mRNA termini

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Abstract
Tomatobushy stunt virus is a (+)-strand RNA virus that is neither 5′-capped nor 3′-polyadenylated. Translation of viral proteins is instead mediated by an RNA element, the 3′-cap–independent translational enhancer (3′CITE), which is located in its 3′ untranslated region (UTR). The 3′CITE is proposed to recruit the translational machinery to the viral message, while a long-distance RNA–RNA interaction between the 3′CITE and 5′ UTR is thought to deliver the 43S ribosomal subunit to the 5′ end of the viral mRNA. Here we provide the first evidence that the 5′ UTR and 3′CITE interact physically. Mutational analysis showed that formation of this RNA–RNA interaction in vitro correlates well with efficient translation in vivo, thus supporting its functional relevance. Other analyses of the 3′CITE confirmed an overall Y-shaped RNA secondary structure and demonstrated the importance of numerous minor structural features for efficient translation of viral mRNAs. Functional studies on the role of the 5′ UTR revealed that despite the absence of a cap structure, 43S subunits load at the very 5′ end and scan in a 3′ direction. These results indicate that the 5′–3′ RNA–RNA interaction is likely disrupted by scanning ribosomal subunits and suggest a dynamic model for the interaction of mRNA termini during active translation.

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