Nuclear localization signals in the core protein of hepatitis C virus

Biochem Biophys Res Commun. 1994 Dec 15;205(2):1284-90. doi: 10.1006/bbrc.1994.2804.

Abstract

The core protein of the hepatitis C virus is derived from the N-terminal 191 amino acids of the viral polyprotein by proteolytic cleavage. In the current study, subcellular localizations of the HCV core and its beta-galactosidase fusion proteins in transfected cells were examined by indirect immunofluorescence and cytochemical staining. The core protein was located predominantly in the cytoplasm 6 days after a plasmid encoding the full-length core protein had been introduced into mammalian cells. A hydrophobic domain in the C-terminal region of the core protein may block the efficiency of nuclear transport, since a beta-galactosidase fusion protein that contains HCV core protein lacking the C-terminal 66-amino-acid was located within the nuclei of mammalian cells 24 hours posttransfection. Three independent nuclear localization signals were further identified in the N-terminal region of the HCV core protein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Carcinoma, Hepatocellular
  • Cell Line
  • Cell Nucleus / metabolism*
  • Chlorocebus aethiops
  • DNA Primers
  • Fluorescent Antibody Technique
  • Hepacivirus / metabolism*
  • Humans
  • Kidney
  • Liver Neoplasms
  • Molecular Sequence Data
  • Polymerase Chain Reaction
  • Recombinant Fusion Proteins / analysis
  • Recombinant Fusion Proteins / biosynthesis
  • Signal Transduction
  • Transfection
  • Tumor Cells, Cultured
  • Viral Core Proteins / analysis
  • Viral Core Proteins / biosynthesis*
  • beta-Galactosidase / biosynthesis

Substances

  • DNA Primers
  • Recombinant Fusion Proteins
  • Viral Core Proteins
  • nucleocapsid protein, Hepatitis C virus
  • beta-Galactosidase