Bioinformatic and Physical Characterizations of Genome-Scale Ordered RNA Structure in Mammalian RNA Viruses
- 1 December 2008
- journal article
- research article
- Published by American Society for Microbiology in Journal of Virology
- Vol. 82 (23) , 11824-11836
- https://doi.org/10.1128/jvi.01078-08
Abstract
By the analysis of thermodynamic RNA secondary structure predictions, we previously obtained evidence for evolutionarily conserved large-scale ordering of RNA virus genomes (P. Simmonds, A. Tuplin, and D. J. Evans, RNA 10:1337-1351, 2004). Genome-scale ordered RNA structure (GORS) was widely distributed in many animal and plant viruses, much greater in extent than RNA structures required for viral translation or replication, but in mammalian viruses was associated with host persistence. To substantiate the existence of large-scale RNA structure differences between viruses, a large set of alignments of mammalian RNA viruses and rRNA sequences as controls were examined by thermodynamic methods (to calculate minimum free energy differences) and by algorithmically independent RNAz and Pfold methods. These methods produced generally concordant results and identified substantial differences in the degrees of evolutionarily conserved, sequence order-dependent RNA secondary structure between virus genera and groups. A probe hybridization accessibility assay was used to investigate the physical nature of GORS. Transcripts of hepatitis C virus (HCV), hepatitis G virus/GB virus-C (HGV/GBV-C), and murine norovirus, which are predicted to be structured, were largely inaccessible to hybridization in solution, in contrast to the almost universal binding of probes to a range of unstructured virus transcripts irrespective of G+C content. Using atomic force microscopy, HCV and HGV/GBV-C RNA was visualized as tightly compacted prolate spheroids, while under the same experimental conditions the predicted unstructured poliovirus and rubella virus RNA were pleomorphic and had extensively single-stranded RNA on deposition. Bioinformatic and physical characterization methods both identified fundamental differences in the configurations of viral genomic RNA that may modify their interactions with host cell defenses and their ability to persist.Keywords
This publication has 53 references indexed in Scilit:
- Bioinformatic and functional analysis of RNA secondary structure elements among different genera of human and animal calicivirusesNucleic Acids Research, 2008
- Murine Noroviruses Comprising a Single Genogroup Exhibit Biological Diversity despite Limited Sequence DivergenceJournal of Virology, 2007
- The RNAz web server: prediction of thermodynamically stable and evolutionarily conserved RNA structuresNucleic Acids Research, 2007
- Size, shape, and flexibility of RNA structuresThe Journal of Chemical Physics, 2006
- RIG-I-Mediated Antiviral Responses to Single-Stranded RNA Bearing 5'-PhosphatesScience, 2006
- 5'-Triphosphate RNA Is the Ligand for RIG-IScience, 2006
- Identification of microRNAs of the herpesvirus familyNature Methods, 2005
- The RNA helicase RIG-I has an essential function in double-stranded RNA-induced innate antiviral responsesNature Immunology, 2004
- The gene-silencing efficiency of siRNA is strongly dependent on the local structure of mRNA at the targeted regionBiochemical and Biophysical Research Communications, 2004
- Multiple Secondary Structure Rearrangements during HIV-1 RNA DimerizationBiochemistry, 2002