Transcription of the hepatitis B surface antigen gene in mouse cells transformed with cloned viral DNA

J Virol. 1982 Apr;42(1):100-5. doi: 10.1128/JVI.42.1.100-105.1982.

Abstract

Mouse L cells transformed with recombinant plasmids carrying hepatitis B virus (HBV) DNA fragments were used to study the transcription of the viral surface antigen gene (gene S). An HBV-specific, polyadenylated, 2.3-kilobase RNA was mapped on the HBV genome. This RNA hybridized with approximately 75% of the genome and excluded the region of the HBV core antigen gene (gene C). The 2.3-kilobase RNA species was present only in cell lines that produced hepatitis B surface antigen. An HBV-specific 2.3-kilobase RNA was also detected in human hepatoma cell line PLC/PRF/5 which produced hepatitis B surface antigen. A study of gene S expression in the transformed mouse L cells allowed us to localize the regions of initiation and termination of gene S transcription. Our results strongly suggest that the 2.3-kilobase RNA molecule is the mRNA of the major polypeptide of the envelope, which carries the viral surface antigen determinants.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cloning, Molecular
  • DNA, Viral / genetics*
  • Genes, Viral
  • Hepatitis B Surface Antigens / genetics*
  • Hepatitis B virus / genetics*
  • L Cells / metabolism
  • Mice
  • Operon
  • Plasmids
  • RNA, Messenger / genetics
  • RNA, Viral / genetics
  • Transcription, Genetic
  • Transformation, Genetic

Substances

  • DNA, Viral
  • Hepatitis B Surface Antigens
  • RNA, Messenger
  • RNA, Viral