Active transcription of the human FAS/CD95/TNFRSF6 gene involves the p53 family

Biochem Biophys Res Commun. 2009 Sep 18;387(2):399-404. doi: 10.1016/j.bbrc.2009.07.063. Epub 2009 Jul 16.

Abstract

p63 and p73 express two main classes of isoforms: isoforms which contain the transactivation domain (TAp73 and TAp63) executing transcriptional activity and dominant-negative isoforms which are truncated at the NH2-terminus acting as operant inhibitors of TAp73, TAp63 and wild-type p53, and thus possessing oncogenic potential. Like wt p53, TAp63 and TAp73 isoforms transactivate target genes that activate apoptosis signaling pathways. In an attempt to understand how the CD95 gene is regulated by the p53 family, we investigated the contributions of a p53-responsive element (RE) within the first intron of the CD95 gene as well as three elements within the promoter. The intronic element conferred transcriptional activation by p53, TAp63 and TAp73 and cooperated with the p53-REs in the promoter of the CD95 gene. Cooperation between the p53-REs in the promoter and the intronic p53-binding site resulted in maximal transcriptional activation of the CD95 gene by the p53 family.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Binding Sites
  • Cell Line, Tumor
  • DNA-Binding Proteins / metabolism
  • Humans
  • Introns
  • Molecular Sequence Data
  • Nuclear Proteins / metabolism
  • Promoter Regions, Genetic
  • Trans-Activators / metabolism
  • Transcription Factors
  • Transcription, Genetic*
  • Transcriptional Activation*
  • Tumor Protein p73
  • Tumor Suppressor Protein p53 / metabolism*
  • Tumor Suppressor Proteins / metabolism
  • fas Receptor / genetics*

Substances

  • DNA-Binding Proteins
  • FAS protein, human
  • Nuclear Proteins
  • TP63 protein, human
  • TP73 protein, human
  • Trans-Activators
  • Transcription Factors
  • Tumor Protein p73
  • Tumor Suppressor Protein p53
  • Tumor Suppressor Proteins
  • fas Receptor