Abstract

Tomato bushy stunt virus (TBSV) is the prototypical member of the genus Tombusvirus in the family Tombusviridae. The (+)-strand RNA genome of TBSV lacks both a 5' cap and a 3' poly(A) tail and instead contains a 3'-terminal RNA sequence that acts as a cap-independent translational enhancer (3' CITE). In this study, we have determined the RNA secondary structure of the translation-specific central segment of the 3' CITE, termed region 3.5 (R3.5). MFOLD structural modeling combined with solution structure mapping and comparative sequence analysis indicate that R3.5 adopts a branched structure that contains three major helices. Deletion and substitution studies revealed that two of these extended stem-loop (SL) structures are essential for 3' CITE activity in vivo. In particular, the terminal loop of one of these SLs, SL-B, was found to be critical for translation. Compensatory mutational analysis showed that SL-B functions by base pairing with another SL, SL3, in the 5' untranslated region of the TBSV genome. Thus, efficient translation of TBSV mRNA in vivo requires a 5'-3' RNA-RNA interaction that effectively circularizes the message. Similar types of interactions are also predicted to occur in TBSV subgenomic mRNAs between their 5' untranslated regions and the 3' CITE, and both genomic and subgenomic 5'-3' interactions are well conserved in all members of the genus Tombusvirus. In addition, a survey of other genera in Tombusviridae revealed the potential for similar 5'-3' RNA-RNA-based interactions in their viral mRNAs, suggesting that this mechanism extends throughout this large virus family.

Highlights

  • Tomato bushy stunt virus (TBSV) is the prototypical member of the genus Tombusvirus in the family Tombusviridae

  • Similar types of interactions are predicted to occur in TBSV subgenomic mRNAs between their 5؅ untranslated regions and the 3؅ CITE, and both genomic and subgenomic 5؅-3؅ interactions are well conserved in all members of the genus Tombusvirus

  • RNA Secondary Structure of R3.5—The 3Ј cap-independent translational enhancer (3Ј CITE) is composed of three contiguous regions that were defined on the basis of their presence (RIII and RIV) or absence (R3.5) in prototypical

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Summary

A POTENTIAL COMMON MECHANISM FOR TOMBUSVIRIDAE*

Eukaryotic (ϩ)-strand RNA viruses must either possess a 5Ј cap and 3Ј poly(A) tail or adopt alternative strategies that allow for efficient translation of their encoded viral proteins [1, 2] In this regard, translationally active viral RNA genomes have been identified that do not contain one or both of these terminal mRNAs structures. To compensate for the absence of both a 5Ј cap and a 3Ј poly(A) tail [11, 14, 15], BYDV1 (genus Luteovirus) [16, 17] and several members of the large family Tombusviridae, including STNV (genus Necrovirus) [18, 19], TBSV (genus Tombusvirus) [20, 21], TCV (genus Carmovirus) [22], Hibiscus chlorotic ringspot virus (genus Carmovirus) [23], and RCNMV (genus Dianthovirus) [24] contain RNA sequences in the 3Ј region of their genomes that function as translational enhancers (TEs). This type of RNA-based mechanism may be used by other genera in the family Tombusviridae

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