A novel p53-inducible apoptogenic gene, PRG3, encodes a homologue of the apoptosis-inducing factor (AIF)

  • Yoichi Ohiro
  • , Igor Garkavtsev
  • , Shinichiro Kobayashi
  • , Kodangattil R. Sreekumar
  • , Regan Nantz
  • , Bryan T. Higashikubo
  • , Shannon L. Duffy
  • , Ryuji Higashikubo
  • , Anny Usheva
  • , David Gius
  • , Nikolai Kley
  • , Nobuo Horikoshi

Research output: Contribution to journalArticlepeer-review

Abstract

The p53 tumor suppressor protein induces cell cycle arrest or apoptosis in response to cellular stresses. We have identified PRG3 (p53-responsive gene 3), which is induced specifically under p53-dependent apoptotic conditions in human colon cancer cells, and encodes a novel polypeptide of 373 amino acids with a predicted molecular mass of 40.5 kDa. PRG3 has significant homology to bacterial oxidoreductases and the apoptosis-inducing factor, AIF, and the gene was assigned to chromosome 10q21.3-q22.1. Expression of PRG3 was induced by the activation of endogenous p53 and it contains a p53-responsive element. Unlike AIF, PRG3 localizes in the cytoplasm and its ectopic expression induces apoptosis. An amino-terminal deletion mutant of PRG3 that lacks a putative oxidoreductase activity retains its apoptotic activity, suggesting that the oxidoreductase activity is dispensable for the apoptotic function of PRG3. The PRG3 gene is thus a novel p53 target gene in a p53-dependent apoptosis pathway.

Original languageEnglish (US)
Pages (from-to)163-171
Number of pages9
JournalFEBS Letters
Volume524
Issue number1-3
DOIs
StatePublished - Jul 31 2002
Externally publishedYes

Keywords

  • Apoptosis
  • Cloning
  • Oxidoreductase
  • Target gene
  • Transcription
  • p53

ASJC Scopus subject areas

  • Biophysics
  • Structural Biology
  • Biochemistry
  • Molecular Biology
  • Genetics
  • Cell Biology

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