Increased synthesis of polycistronic mRNA associated with increased polyadenylation by vesicular stomatitis virus

Virology. 1992 Jul;189(1):67-78. doi: 10.1016/0042-6822(92)90682-f.

Abstract

Electron microscopy suggested that the mRNA produced in vitro by tsG16(I), a temperature-sensitive mutant of vesicular stomatitis virus, contained an increased proportion of polycistronic mRNAs. Using hybrid selection, we found that the poly(A)+ mRNA synthesized in vitro by tsG16(I) contained approximately two to three times more polycistronic mRNA than did poly(A)+ mRNA synthesized in vitro by the parental wild-type (wt) virus. The increase in polycistronic mRNA occurred at all intergenic junctions examined. In vitro, tsG16(I) has an increased polyadenylation phenotype and a temperature-sensitive transcriptase activity that appear to be due to different mutations. Partial revertants of tsG16(I), which have lost the aberrant polyadenylation phenotype but retain the in vitro thermosensitive transcriptase, produced wt amounts of polycistronic mRNA. This suggested that the increased production of polycistronic mRNA by tsG16(I) may be associated with the increased polyadenylation phenotype of this mutant. These data further support the hypothesis that an increase in size of poly(A) tracts is associated with increased production of polycistronic mRNA.

Publication types

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

MeSH terms

  • Base Sequence
  • Chromosome Mapping
  • Genes, Viral / genetics*
  • Microscopy, Electron
  • Molecular Sequence Data
  • Mutation
  • Nucleic Acid Hybridization
  • Poly A / metabolism*
  • RNA, Messenger / drug effects
  • RNA, Messenger / metabolism*
  • RNA, Messenger / ultrastructure
  • RNA-Directed DNA Polymerase / genetics
  • RNA-Directed DNA Polymerase / metabolism
  • Reading Frames / genetics
  • S-Adenosylhomocysteine / pharmacology
  • Transcription, Genetic* / drug effects
  • Vesicular stomatitis Indiana virus / metabolism*
  • Viral Structural Proteins / genetics*

Substances

  • RNA, Messenger
  • Viral Structural Proteins
  • Poly A
  • S-Adenosylhomocysteine
  • RNA-Directed DNA Polymerase