Mutations within noncoding terminal sequences of model RNAs of Sendai virus: influence on reporter gene expression

J Virol. 1995 Aug;69(8):5128-31. doi: 10.1128/JVI.69.8.5128-5131.1995.

Abstract

A reverse-genetics system employing the chloramphenicol acetyltransferase (CAT) reporter gene has been established previously for Sendai virus. We utilized PCR-directed mutagenesis to introduce nucleotide additions, deletions, and/or substitutions within terminal Sendai virus RNA sequences. The influence of these mutations on replication-transcription of these model Sendai-CAT RNAs was analyzed by assaying CAT activity. Results from these experiments indicate that (i) Sendai-CAT RNAs expressing wild-type levels of CAT activity conform to the Sendai virus rule of six, (ii) apparent exceptions to the rule of six exist in that the 5' terminus of the Sendai-CAT RNA is more tolerant than the 3' terminus of nucleotide additions or deletions, and (iii) the 3' leader region of Sendai-CAT RNA appears to be sensitive not only to mutagenesis (single-nucleotide addition or deletion) but also to changes in its total nucleotide length.

Publication types

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

MeSH terms

  • Base Sequence
  • Chloramphenicol O-Acetyltransferase / genetics
  • Gene Expression*
  • Genes, Reporter*
  • Molecular Sequence Data
  • Mutagenesis, Insertional
  • Parainfluenza Virus 1, Human / genetics*
  • RNA, Viral / genetics*
  • Sequence Deletion

Substances

  • RNA, Viral
  • Chloramphenicol O-Acetyltransferase