APAF-1 is a transcriptional target of p53 in DNA damage-induced apoptosis

Cancer Res. 2001 Sep 15;61(18):6660-4.

Abstract

The expression of genes involved in p53-mediated apoptosis was studied using cDNA microarray after treating isogenic cell lines with either ionizing radiation or doxorubicin. Most of the known p53 transcriptional activation target genes clustered in a functional category defined by early and p53-dependent induction, regardless of the type of stress. Apoptotic protease activating factor-1 (APAF-1) emerged from this analysis as a novel p53 target gene. Genomic sequences upstream of the APAF-1 transcription start site contain a classic p53-responsive element that bound to p53. Consistently, p53 directly induced APAF-1 gene expression. Furthermore, DNA damage-mediated induction of APAF-1 mRNA and protein expression, accompanied by apoptosis, were strictly dependent on wild-type p53 function. These data are consistent with the hypothesis that APAF-1 is an essential downstream effector of p53-mediated apoptosis.

MeSH terms

  • Apoptosis / genetics*
  • Apoptotic Protease-Activating Factor 1
  • Cell Line
  • Colorectal Neoplasms / genetics
  • Colorectal Neoplasms / pathology
  • DNA Damage*
  • Gene Expression Profiling
  • Humans
  • Lymphocytes / drug effects
  • Lymphocytes / physiology
  • Lymphocytes / radiation effects
  • Multigene Family
  • Oligonucleotide Array Sequence Analysis
  • Proteins / genetics*
  • Transcriptional Activation / drug effects
  • Transcriptional Activation / genetics
  • Transcriptional Activation / radiation effects
  • Tumor Cells, Cultured
  • Tumor Suppressor Protein p53 / genetics*

Substances

  • APAF1 protein, human
  • Apoptotic Protease-Activating Factor 1
  • Proteins
  • Tumor Suppressor Protein p53