Human AP endonuclease possesses a significant activity as major 3'-5' exonuclease in human leukemia cells

Biochem Biophys Res Commun. 2003 Oct 17;310(2):522-8. doi: 10.1016/j.bbrc.2003.09.033.

Abstract

Apurinic/apyrimidinic (AP) endonuclease (Ape1) is the major cellular enzyme responsible for repairing AP-sites in DNA. It can cleave the DNA phosphodiester backbone immediately 5(') to an AP-site. Ape1 also shows 3(')-phosphodiesterase activity, a 3(')-phosphatase activity, and an RNaseH activity. However, regarding its exonuclease activity, it remains controversial whether human Ape1 may possess a 3(')-5(') exonuclease activity. During the course of study to search for the major nuclease activity to double-stranded DNA in human leukemia cells, we purified a 37 kDa Mg(2+)-dependent exonuclease from cytosolic fraction of human leukemia U937 cells. Surprisingly, this exonuclease is Ape1. We demonstrated for the first time that Ape1 possesses a significant activity as major 3(')-5(') exonuclease in human leukemia cells. In addition, we also observed that translocation of cytoplasmic Ape1 into nucleus occurs during DNA damage.

MeSH terms

  • Cell Nucleus / enzymology
  • Cytoplasm / enzymology
  • DNA-(Apurinic or Apyrimidinic Site) Lyase / analysis
  • DNA-(Apurinic or Apyrimidinic Site) Lyase / metabolism*
  • Exodeoxyribonucleases / analysis
  • Exodeoxyribonucleases / metabolism*
  • Humans
  • Leukemia / enzymology*
  • U937 Cells

Substances

  • Exodeoxyribonucleases
  • APEX1 protein, human
  • DNA-(Apurinic or Apyrimidinic Site) Lyase