Abstract

20S RNA narnavirus is a positive strand RNA virus found in the yeast Saccharomyces cerevisiae. The viral genome (2514 nucleotides) only encodes a single protein (p91), the RNA-dependent RNA polymerase and does not have capsid proteins to form intracellular virions. The genomic RNA has no 3' poly(A) tail and perhaps no cap structure at the 5'-end; thus resembling an intermediate of mRNA degradation. The virus, however, escapes the host surveillance and replicates in the yeast cytoplasm persistently. The viral genome is not naked but exists in the form of a ribonucleoprotein complex with p91 in a 1:1 stoichiometry. Here we investigated interactions between p91 and the viral genome. Our results indicate that p91 directly or indirectly interacts with the RNA at the 5'- and 3'-end regions and to a lesser extent at a central part. The 3'-end site is identical to or overlaps with the 3' cis signal for replication identified previously. The 5'-site is at the second stem loop structure from the 5'-end (nucleotides 72-104), and this structure also contains a cis signal for replication. Analysis of mutants in the structure revealed a tight correlation between replication and formation of complexes. These results highlight the importance of ribonucleoprotein complexes for the viral life cycle. We will discuss implications of these findings especially on how the virus escapes from mRNA degradation pathways and resides in the cytoplasm persistently despite the lack of a protective capsid.

Highlights

  • Have extensively been studied, intracellular events leading to the maintenance and stable replication of the viral genome remain to be elucidated

  • 20S RNA narnavirus is a persistent positive strand RNA virus found in most laboratory strains of the yeast Saccharomyces cerevisiae [2, 3]

  • Further studies showed that most of the genomic strands exist in the form of ribonucleoprotein complexes with p91 in a 1:1 stoichiometry [13], suggesting that formation of these complexes is a key factor for the stabilization of the viral genome inside of the cell

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Summary

EXPERIMENTAL PROCEDURES

Immunoprecipitation of RNase-treated 20S RNA/p91 were performed as described in Ref. 19. NaCl, 0.05% Tween 20) containing 5 mM MgCl2, and digested onto a Nytran N membrane, and 20S RNA transcripts on the for 10 min at 25 °C with different concentrations of RNase A membrane were detected by hybridization. RNA was extracted directly from the lysates (Total RNA), slot-blotted, and hybridized with either the 20S RNA-specific probe or the 32P-labeled oligonucleotide RE368 (5Ј-CCTCATAAAACTGATACGAGCTTCTGCTATCC-3Ј) complementary to nt 963–994 in 25S rRNA. The latter was used to detect 25S rRNA as a loading control.

RESULTS
Findings
DISCUSSION
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