Poliovirus requires a precise 5' end for efficient positive-strand RNA synthesis

J Virol. 2000 Jul;74(14):6394-400. doi: 10.1128/jvi.74.14.6394-6400.2000.

Abstract

Poliovirus infectious RNA can be synthesized in vitro using phage DNA-dependent RNA-polymerases. These synthetic transcripts contain several extra nucleotides at the 5' end, which are deleted during replication to generate authentic viral genomes. We removed those 5'-end extra nucleotides utilizing a hammerhead ribozyme to produce transcripts with accurate 5' ends. These transcripts replicate substantially more rapidly in cell culture, demonstrating no lag before replication; they also replicate more efficiently in Xenopus laevis oocytes and in in vitro translation-replication cell extracts. In both systems, an exact 5' end is necessary for synthesis of positive-strand RNA but not negative-strand RNA.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cell Extracts
  • Cell Line
  • Humans
  • In Vitro Techniques
  • Oocytes / virology
  • Poliovirus / genetics
  • Poliovirus / metabolism*
  • Poliovirus / physiology
  • RNA, Catalytic / metabolism
  • RNA, Viral / biosynthesis*
  • RNA, Viral / chemistry
  • Virus Replication
  • Xenopus laevis

Substances

  • Cell Extracts
  • RNA, Catalytic
  • RNA, Viral