Key result
A long-range RNA-RNA interaction spanning ~3000 nucleotides in the tombusvirus genome facilitates efficient assembly of the viral RNA replicase and is essential for viral genome replication.
A long-range RNA-RNA interaction spanning ~3000 nucleotides forms a discontinuous RNA platform essential for tombusvirus RNA replicase assembly and genome replication.
May inform RNA-targeted antiviral design; leaves open validation in human viral systems.
Plus-strand RNA viruses contain RNA elements within their genomes that mediate a variety of fundamental viral processes. The traditional view of these elements is that of local RNA structures. This perspective, however, is changing due to increasing discoveries of functional viral RNA elements that are formed by long-range RNA-RNA interactions, often spanning thousands of nucleotides. The plus-strand RNA genomes of tombusviruses exemplify this concept by possessing different long-range RNA-RNA interactions that regulate both viral translation and transcription. Here we report that a third fundamental tombusvirus process, viral genome replication, requires a long-range RNA-based interaction spanning approximately 3000 nts. In vivo and in vitro analyses suggest that the discontinuous RNA platform formed by the interaction facilitates efficient assembly of the viral RNA replicase. This finding has allowed us to build an integrated model for the role of global RNA structure in regulating the reproduction of a eukaryotic RNA virus, and the insights gained have extended our understanding of the multifunctional nature of viral RNA genomes.
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Wu et al. (2009) studied Tombusvirus infection. Mutational analysis of UL-DL RNA interaction vs. Wild-type viral genome was evaluated on Viral RNA genome accumulation and replicase assembly. A long-range RNA-RNA interaction spanning ~3000 nucleotides in the tombusvirus genome facilitates efficient assembly of the viral RNA replicase and is essential for viral genome replication.
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