In vitro secondary structure of the genomic RNA of satellite tobacco mosaic virus.

TitleIn vitro secondary structure of the genomic RNA of satellite tobacco mosaic virus.
Publication TypeJournal Article
Year of Publication2013
AuthorsAthavale, SS, J Gossett, J, Bowman, JC, Hud, NV, Williams, LDean, Harvey, SC
JournalPLoS One
Volume8
Issue1
Paginatione54384
Date Published2013
ISSN1932-6203
KeywordsBase Pairing, Genome, Nucleic Acid Conformation, RNA, Transfer, RNA, Viral, Tobacco, Tobacco mosaic satellite virus, Virion
Abstract

Satellite tobacco mosaic virus (STMV) is a T = 1 icosahedral virus with a single-stranded RNA genome. It is widely accepted that the RNA genome plays an important structural role during assembly of the STMV virion. While the encapsidated form of the RNA has been extensively studied, less is known about the structure of the free RNA, aside from a purported tRNA-like structure at the 3' end. Here we use selective 2'-hydroxyl acylation analyzed by primer extension (SHAPE) analysis to examine the secondary structure of in vitro transcribed STMV RNA. The predicted secondary structure is unusual in the sense that it is highly extended, which could be significant for protecting the RNA from degradation. The SHAPE data are also consistent with the previously predicted tRNA-like fold at the 3' end of the molecule, which is also known to hinder degradation. Our data are not consistent with the secondary structure proposed for the encapsidated RNA by Schroeder et al., suggesting that, if the Schroeder structure is correct, either the RNA is packaged as it emerges from the replication complex, or the RNA undergoes extensive refolding upon encapsidation. We also consider the alternative, i.e., that the structure of the encapsidated STMV RNA might be the same as the in vitro structure presented here, and we examine how this structure might be organized in the virus. This possibility is not rigorously ruled out by the available data, so it remains open to examination by experiment.

DOI10.1371/journal.pone.0054384
Alternate JournalPLoS ONE
PubMed ID23349871
PubMed Central IDPMC3551766
Grant ListGM 70785 / GM / NIGMS NIH HHS / United States