Human immunodeficiency virus type 1 gag-pol frameshifting is dependent on downstream mRNA secondary structure: demonstration by expression in vivo. Academic Article uri icon

Overview

abstract

  • The human immunodeficiency virus type 1 (HIV-1) Gag-Pol fusion polyprotein is produced via ribosomal frameshifting. Previous studies in vitro and in Saccharomyces cerevisiae have argued against a significant role for RNA secondary structure 3' of the shift site, in contrast with other systems, in which such structure has been shown to be required. Here we show, by expressing the HIV-1 gag-pol domain in cultured vertebrate cells, that a stem-loop structure 3' of the HIV-1 shift site is indeed important for wild-type levels of frameshifting in vivo.

publication date

  • August 1, 1992

Research

keywords

  • Frameshift Mutation
  • Fusion Proteins, gag-pol
  • Genes, gag
  • Genes, pol
  • HIV-1
  • RNA, Messenger

Identity

PubMed Central ID

  • PMC241392

Scopus Document Identifier

  • 0026717107

Digital Object Identifier (DOI)

  • 10.1128/JVI.66.8.5147-5151.1992

PubMed ID

  • 1321294

Additional Document Info

volume

  • 66

issue

  • 8