p73 is transcriptionally regulated by DNA damage, p53, and p73

Oncogene. 2001 Feb 8;20(6):769-74. doi: 10.1038/sj.onc.1204149.


p73 is a member of the p53 family. Recent studies have shown that DNA damage can stabilize p73 protein and enhance p73-mediated apoptosis in a c-Abl dependent manner. To determine what regulates p73 transcriptionally, we analysed the expression of p73 in several cell lines following genotoxic stresses. We found that p73 is induced in certain cell lines when treated with therapeutic DNA damaging agents. We also found that p53 and p73, but not mutant p53(R249S) and p73beta292, directly induce the expression of the p73 gene. In addition, we found one potential p53-binding site in the promoter of the p73 gene. This binding site is responsive to p53, p73, and DNA damage. Taken together, these data suggest that p73 is transcriptionally regulated by DNA damage and p53, and is autoregulated.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Base Sequence
  • DNA Damage*
  • DNA-Binding Proteins / genetics*
  • Gene Expression Regulation
  • Genes, Tumor Suppressor
  • Molecular Sequence Data
  • Mutagens / pharmacology
  • Nuclear Proteins / genetics*
  • Response Elements
  • Transcription, Genetic
  • Tumor Cells, Cultured
  • Tumor Protein p73
  • Tumor Suppressor Protein p53 / genetics*
  • Tumor Suppressor Proteins


  • Antineoplastic Agents
  • DNA-Binding Proteins
  • Mutagens
  • Nuclear Proteins
  • Tumor Protein p73
  • Tumor Suppressor Protein p53
  • Tumor Suppressor Proteins