Literature DB >> 18638511

Role of tRNA-like structures in controlling plant virus replication.

Theo W Dreher1.   

Abstract

Transfer RNA-like structures (TLSs) that are sophisticated functional mimics of tRNAs are found at the 3'-termini of the genomes of a number of plant positive strand RNA viruses. Three natural aminoacylation identities are represented: valine, histidine, and tyrosine. Paralleling this variety in structure, the roles of TLSs vary widely between different viruses. For Turnip yellow mosaic virus, the TLS must be capable of valylation in order to support infectivity, major roles being the provision of translational enhancement and down-regulation of minus strand initiation. In contrast, valylation of the Peanut clump virus TLS is not essential. An intermediate situation seems to exist for Brome mosaic virus, whose RNAs 1 and 2, but not RNA 3, need to be capable of tyrosylation to support infectivity. Other known roles for certain TLSs include: (i) the recruitment of host CCA nucleotidyltransferase as a telomerase to maintain intact 3' CCA termini, (ii) involvement in the encapsidation of viral RNAs, and (iii) presentation of minus strand promoter elements for replicase recognition. In the latter role, the promoter elements reside within the TLS but are not functionally dependent on tRNA mimicry. The phylogenetic distribution of TLSs indicates that their evolutionary history includes frequent horizontal exchange, as has been observed for protein-coding regions of plant positive strand RNA viruses.

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Year:  2008        PMID: 18638511      PMCID: PMC2676847          DOI: 10.1016/j.virusres.2008.06.010

Source DB:  PubMed          Journal:  Virus Res        ISSN: 0168-1702            Impact factor:   3.303


  118 in total

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Journal:  Virology       Date:  1991-01       Impact factor: 3.616

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Authors:  J B Goodwin; T W Dreher
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Authors:  R Giegé; C Florentz; T W Dreher
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9.  Comparison and functional implications of the 3D architectures of viral tRNA-like structures.

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10.  RNA-based regulation of transcription and translation of aureusvirus subgenomic mRNA1.

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