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Non-replicating vaccinia vector efficiently expresses bacteriophage T7 RNA polymerase.

Abstract
Modified vaccinia virus Ankara (MVA), a host range restricted and highly attenuated vaccinia virus strain, is unable to multiply in human and most other mammalian cell lines. Since viral gene expression is unimpaired in non-permissive cells recombinant MVA viruses are efficient as well as exceptionally safe expression vectors. We constructed a recombinant MVA that expresses the bacteriophage T7 RNA polymerase and tested its usefulness for transient expression of recombinant genes under the control of a T7 promoter. Using the chloramphenicol acetyltransferase (CAT) gene as a reporter gene, infection with MVA-T7pol allowed efficient synthesis of recombinant enzyme in mammalian cells. Despite the severe host restriction of MVA, enzyme activities induced by infection with MVA-T7pol were similar to those determined after infection with a replication-competent vaccinia-T7pol recombinant virus. Thus, MVA-T7pol may be used as a novel vaccinia vector to achieve T7 RNA polymerase-specific recombinant gene expression in the absence of productive vaccinia virus replication.
AuthorsG Sutter, M Ohlmann, V Erfle
JournalFEBS letters (FEBS Lett) Vol. 371 Issue 1 Pg. 9-12 (Aug 28 1995) ISSN: 0014-5793 [Print] England
PMID7664891 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Recombinant Fusion Proteins
  • Viral Proteins
  • Chloramphenicol O-Acetyltransferase
  • bacteriophage T7 RNA polymerase
  • DNA-Directed RNA Polymerases
  • beta-Galactosidase
Topics
  • Animals
  • Base Sequence
  • Cells, Cultured
  • Chick Embryo
  • Chloramphenicol O-Acetyltransferase (biosynthesis, genetics)
  • DNA-Directed RNA Polymerases (biosynthesis, genetics)
  • Fibroblasts
  • Gene Expression Regulation, Viral (genetics)
  • Genes, Reporter (genetics)
  • Genetic Vectors (genetics)
  • Haplorhini
  • HeLa Cells
  • Humans
  • Molecular Sequence Data
  • Promoter Regions, Genetic (genetics)
  • Recombinant Fusion Proteins (genetics)
  • Vaccinia virus (genetics, physiology)
  • Viral Proteins
  • Virus Replication
  • beta-Galactosidase (biosynthesis)

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