cis Acting RNA sequences control the gag-pol translation readthrough in murine leukemia virus

Virology. 1991 Jul;183(1):313-9. doi: 10.1016/0042-6822(91)90144-z.

Abstract

The pol gene of the Moloney murine leukemia virus (M-MuLV) is expressed as a Gag-Pol fusion protein through an in-frame suppression of the UAG termination codon located between the two genes. The role of nucleotide context in suppression was investigated, in a rabbit reticulocyte lysate translation system, using site-directed mutagenesis. The results indicate that the translational readthrough is mediated by at least 50 bases long RNA sequence located 3' to the gag UAG termination codon. Within this sequence a short purine-rich sequence adjacent to the amber codon, highly conserved among different retroviruses, appears essential for M-MuLV suppression. Two alternative putative stem and loop like RNA structures can be drawn at the gag-pol junction, one abutting the gag UAG codon, and the second downstream to it. None of these structures appears to be important to the suppression process.

MeSH terms

  • Animals
  • Base Sequence
  • Codon
  • Fusion Proteins, gag-pol / genetics*
  • Gene Expression Regulation, Viral
  • Genes, gag
  • Genes, pol
  • Molecular Sequence Data
  • Moloney murine leukemia virus / genetics*
  • Mutagenesis, Site-Directed
  • Nucleic Acid Conformation
  • Protein Biosynthesis*
  • RNA, Viral / chemistry*
  • Rabbits
  • Regulatory Sequences, Nucleic Acid*
  • Reticulocytes / metabolism
  • Suppression, Genetic
  • Terminator Regions, Genetic

Substances

  • Codon
  • Fusion Proteins, gag-pol
  • RNA, Viral