Hepatitis B x protein inhibits p53-dependent DNA repair in primary mouse hepatocytes

S Prost, J M Ford, C Taylor, J Doig, D J Harrison

Research output: Contribution to journalArticlepeer-review

Abstract

The mechanisms by which the hepatitis B x protein (HBx) contributes to hepatocarcinogenesis remain unclear. However, interaction with the tumor suppressor gene p53 and inhibition of p53-dependent cellular functions, including nucleotide excision repair, could be central to this process. We studied the levels of global repair (removal of cyclobutane pyrimidine dimers (CPDs) and 6-4 photoproducts) and transcription-coupled repair (removal of CPDs in both strands of the dihydrofolate reductase gene) in primary wild-type and p53-null mouse hepatocytes. We show that global repair of CPDs appears to be more efficient in mouse hepatocytes than in other commonly studied rodent cells and approaches the levels of human cells and that p53 is required for global genomic DNA repair of CPDs but not for transcription-coupled repair. We then investigated the effect of HBx expression on hepatocyte nucleotide excision repair. We demonstrate that HBx expression affects DNA repair in a p53-dependent manner. Transient HBx expression reduces global DNA repair in wild-type cells to the level of p53-null hepatocytes and has no effect on the repair of a transfected damaged plasmid. Therefore, in viral hepatitis, the hepatitis B virus could inhibit the p53-dependent component of global repair leading, over time, to accumulation of genetic defects and fostering carcinogenesis.
Original languageEnglish
Pages (from-to)33327-32
Number of pages6
JournalJournal of Biological Chemistry
Volume273
Issue number50
Publication statusPublished - 1998

Keywords / Materials (for Non-textual outputs)

  • Animals
  • Cells, Cultured
  • DNA Damage
  • DNA Repair
  • Liver
  • Male
  • Mice
  • Mice, Knockout
  • Trans-Activators
  • Tumor Suppressor Protein p53

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