Involvement of Exo1b in DNA damage-induced apoptosis

Nucleic Acids Res. 2009 Jun;37(10):3452-63. doi: 10.1093/nar/gkp194. Epub 2009 Apr 1.

Abstract

Apoptosis is essential for the maintenance of inherited genomic integrity. During DNA damage-induced apoptosis, mechanisms of cell survival, such as DNA repair are inactivated to allow cell death to proceed. Here, we describe a role for the mammalian DNA repair enzyme Exonuclease 1 (Exo1) in DNA damage-induced apoptosis. Depletion of Exo1 in human fibroblasts, or mouse embryonic fibroblasts led to a delay in DNA damage-induced apoptosis. Furthermore, we show that Exo1 acts upstream of caspase-3, DNA fragmentation and cytochrome c release. In addition, induction of apoptosis with DNA-damaging agents led to cleavage of both isoforms of Exo1. The cleavage of Exo1 was mapped to Asp514, and shown to be mediated by caspase-3. Expression of a caspase-3 cleavage site mutant form of Exo1, Asp514Ala, prevented formation of the previously observed fragment without any affect on the onset of apoptosis. We conclude that Exo1 has a role in the timely induction of apoptosis and that it is subsequently cleaved and degraded during apoptosis, potentially inhibiting DNA damage repair.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis*
  • Caspase 3 / metabolism
  • Cell Line
  • Cytochromes c / metabolism
  • DNA Damage*
  • DNA Fragmentation
  • DNA Repair Enzymes / antagonists & inhibitors
  • DNA Repair Enzymes / metabolism
  • DNA Repair Enzymes / physiology*
  • Exodeoxyribonucleases / antagonists & inhibitors
  • Exodeoxyribonucleases / metabolism
  • Exodeoxyribonucleases / physiology*
  • HeLa Cells
  • Humans
  • Mice
  • Protein Serine-Threonine Kinases / metabolism
  • RNA Interference
  • Ultraviolet Rays

Substances

  • Cytochromes c
  • Protein Serine-Threonine Kinases
  • EXO1 protein, human
  • Exodeoxyribonucleases
  • Caspase 3
  • DNA Repair Enzymes