Abstract
Maintenance of genome integrity is of major importance for plus-stranded RNA viruses that are vulnerable to degradation by host ribonucleases or to replicase errors. We demonstrate that short truncations at the 5' end of a model Tomato bushy stunt virus (TBSV) RNA could be repaired during replication in yeast and plant cells. Although the truncations led to the loss of important cis-regulatory elements, the genome repair mechanisms led to the recovery of promoter and enhancer-like sequences in 92% of TBSV progeny. Using in vitro approaches, we demonstrate that the repaired TBSV RNAs are replication-competent. We propose three different mechanisms for genome repair: initiation of RNA synthesis from internal sequences and addition of nonviral nucleotides by the tombusvirus replicase; and via RNA recombination. The ability to repair cis-sequences makes the tombusvirus genome more flexible, which could be beneficial to increase the virus fitness and adaptation to new hosts.
Original language | English |
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Pages (from-to) | 96-105 |
Number of pages | 10 |
Journal | Virology |
Volume | 404 |
Issue number | 1 |
DOIs | |
State | Published - Aug 2010 |
Bibliographical note
Funding Information:The authors thank Dr. Judit Pogany for her critical review of the manuscript. This work was supported by NSF ( IOB-0517218 ) and the University of Kentucky .
Keywords
- Genome repair
- In vitro RNA synthesis
- Plant protoplast
- RNA promoter
- RNA replication enhancer
- Recombination
- Replication
- Yeast
- Yeast cell-free assay
ASJC Scopus subject areas
- Virology