Mechanism of ribosome shunting in Rice tungro bacilliform pararetrovirus

RNA. 2006 May;12(5):841-50. doi: 10.1261/rna.2285806. Epub 2006 Mar 23.

Abstract

In plant pararetroviruses, pregenomic RNA serves both as a template for replication through reverse transcription and a polysictronic mRNA. This RNA has a complex leader sequence preceding the first large ORF. The leader contains multiple short ORFs and strong secondary structure, both inhibiting ribosome scanning. Translation on this RNA is initiated by shunting, in which scanning ribosomes bypass a large portion of the leader with the inhibitory secondary structure and short ORFs. In Cauliflower mosaic virus (CaMV), the ribosome shunting mechanism involves translation of the 5'-proximal short ORF terminating in front of the secondary structure that appears to force ribosomes to take off and resume scanning at a landing site downstream of the structure. Using two plant protoplast systems and shunt-competent wheat-germ extracts, we demonstrate that in Rice tungro bacilliform virus (RTBV) shunting also depends on the first short ORF followed by strong secondary structure. Swapping of the conserved shunt elements between CaMV and RTBV revealed the importance of nucleotide composition of the landing sequence for efficient shunting. The results suggest that the mechanism of ribosome shunting is evolutionary conserved in plant pararetroviruses.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 5' Untranslated Regions
  • Badnavirus / genetics*
  • Base Sequence
  • Caulimovirus / genetics
  • Chloramphenicol O-Acetyltransferase / metabolism
  • Conserved Sequence
  • DNA, Viral / chemistry
  • DNA, Viral / genetics*
  • Genes, Plant
  • Genes, Reporter
  • In Vitro Techniques
  • Models, Genetic
  • Molecular Sequence Data
  • Nucleic Acid Conformation
  • Open Reading Frames
  • Oryza / virology*
  • Plant Extracts
  • Plant Viruses / genetics*
  • Point Mutation
  • Protein Biosynthesis
  • Protoplasts / metabolism
  • Ribosomes / genetics
  • Ribosomes / metabolism*
  • Transcription, Genetic
  • Triticum

Substances

  • 5' Untranslated Regions
  • DNA, Viral
  • Plant Extracts
  • Chloramphenicol O-Acetyltransferase