Repression of the A8L gene, encoding the early transcription factor 82-kilodalton subunit, inhibits morphogenesis of vaccinia virions

J Virol. 1998 Jan;72(1):104-12. doi: 10.1128/JVI.72.1.104-112.1998.

Abstract

The vaccinia virus early transcription factor (VETF) is a DNA binding protein comprised of 70- and 82-kDa subunits encoded by the D6R and A8L genes, respectively. A previous investigation suggested a novel role for the 70-kDa subunit in the morphogenesis of vaccinia virus particles. The principal objectives of the present study were to determine if the 82-kDa subunit of VETF is also required for morphogenesis and, if so, whether the block occurs before or after the incorporation of the genome into the assembling virus particle. To address these and other questions, we constructed and characterized a conditionally lethal recombinant vaccinia virus in which the A8L gene is stringently repressed by the Escherichia coli lac operator system. The amount of 82-kDa protein synthesized could be regulated by the amount of inducer: from undetectable to higher than normal levels. Virus replication, as determined by plaque formation or virus yield upon synchronous infection, was dependent on inducer. Nevertheless, de novo synthesis of the 82-kDa subunit was not required for viral early, intermediate, and late gene expression or DNA replication. Overexpression of the A8L gene alone, produced by high concentrations of inducer, inhibited viral late protein synthesis, whereas overexpression of the D6R gene alone or both VETF genes simultaneously had little inhibitory effect. Laser confocal fluorescence and quantitative electron microscopic analyses revealed that immature and DNA-containing intermediate stage particles accumulated in the absence of inducer, indicating that the A8L protein has a role in morphogenesis of the core and subsequent events.

MeSH terms

  • Animals
  • Base Sequence
  • Cell Line
  • DNA Primers / genetics
  • DNA, Viral / genetics
  • DNA, Viral / metabolism
  • DNA-Binding Proteins / chemistry
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / physiology
  • Escherichia coli / genetics
  • Gene Expression Regulation, Viral
  • Genes, Viral*
  • HeLa Cells
  • Humans
  • Isopropyl Thiogalactoside / pharmacology
  • Lac Operon
  • Microscopy, Confocal
  • Microscopy, Electron
  • Molecular Weight
  • Mutation
  • Protein Conformation
  • Recombination, Genetic
  • Transcription Factors / chemistry
  • Transcription Factors / genetics*
  • Transcription Factors / physiology
  • Vaccinia virus / genetics*
  • Vaccinia virus / growth & development*
  • Vaccinia virus / physiology
  • Viral Proteins / chemistry
  • Viral Proteins / genetics*
  • Viral Proteins / physiology

Substances

  • DNA Primers
  • DNA, Viral
  • DNA-Binding Proteins
  • Transcription Factors
  • Viral Proteins
  • early transcription factor protein, Vaccinia virus
  • Isopropyl Thiogalactoside