Inhibition of pseudorabies virus replication by a chimeric trans-gene product repressing transcription of the immediate-early gene

Virology. 1995 Jun 20;210(1):128-40. doi: 10.1006/viro.1995.1324.

Abstract

A chimeric gene encoding a fusion protein consisting of the DNA-binding domain of the immediate-early (IE) protein of pseudorabies virus (PRV) and a tail-truncated Vmw65 of herpes simplex virus 1, lacking the transcription activation domain, was constructed. The chimeric gene product inhibited transcription from the PRV IE promoter in a transient expression assay. A HeLa cell line stably transformed with the chimeric gene showed remarkable resistance to PRV infection. In the transformed cells infected with PRV, transcription of the PRV IE gene was repressed, indicating that the resistance of the cells to PRV infection was due to interference with IE gene transcription by the fusion protein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Cell Line, Transformed
  • Chimera
  • Chloramphenicol O-Acetyltransferase / analysis
  • Chloramphenicol O-Acetyltransferase / biosynthesis
  • Gene Expression Regulation, Viral*
  • Genes, Immediate-Early*
  • HeLa Cells
  • Herpes Simplex Virus Protein Vmw65 / biosynthesis
  • Herpes Simplex Virus Protein Vmw65 / metabolism
  • Herpesvirus 1, Human / genetics
  • Herpesvirus 1, Human / physiology
  • Herpesvirus 1, Suid / genetics
  • Herpesvirus 1, Suid / physiology*
  • Humans
  • Immediate-Early Proteins / biosynthesis
  • Immediate-Early Proteins / metabolism*
  • Kinetics
  • Molecular Sequence Data
  • Oligonucleotide Probes
  • Plasmids
  • Promoter Regions, Genetic
  • Recombinant Fusion Proteins / biosynthesis
  • Recombinant Fusion Proteins / metabolism
  • Restriction Mapping
  • Suppression, Genetic
  • Time Factors
  • Transcription, Genetic*
  • Viral Plaque Assay
  • Virus Replication*

Substances

  • Herpes Simplex Virus Protein Vmw65
  • Immediate-Early Proteins
  • Oligonucleotide Probes
  • Recombinant Fusion Proteins
  • Chloramphenicol O-Acetyltransferase