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Cleaving the oxidative repair protein Ape1 enhances cell death mediated by granzyme A.

The cytolytic T lymphocyte protease granzyme A (GzmA) initiates a caspase-independent cell death pathway. Here we report that the rate-limiting enzyme of DNA base excision repair, apurinic endonuclease-1 (Ape1), which is also known as redox factor-1 (Ref-1), binds to GzmA and is contained in the SET complex, a macromolecular complex of 270-420 kDa that is associated with the endoplasmic reticulum and is targeted by GzmA during cell-mediated death. GzmA cleaves Ape1 after Lys31 and destroys its known oxidative repair functions. In so doing, GzmA may block cellular repair and force apoptosis. In support of this, cells with silenced Ape1 expression are more sensitive, whereas cells overexpressing noncleavable Ape1 are more resistant, to GzmA-mediated death.

Pubmed ID: 12524539

Authors

  • Fan Z
  • Beresford PJ
  • Zhang D
  • Xu Z
  • Novina CD
  • Yoshida A
  • Pommier Y
  • Lieberman J

Journal

Nature immunology

Publication Data

February 29, 2003

Associated Grants

None

Mesh Terms

  • Animals
  • Apoptosis
  • Base Sequence
  • Carbon-Oxygen Lyases
  • DNA
  • DNA Repair
  • DNA-(Apurinic or Apyrimidinic Site) Lyase
  • Gene Silencing
  • Granzymes
  • HeLa Cells
  • Humans
  • K562 Cells
  • Macromolecular Substances
  • Membrane Glycoproteins
  • Oxidation-Reduction
  • Perforin
  • Pore Forming Cytotoxic Proteins
  • RNA Interference
  • Recombinant Proteins
  • Serine Endopeptidases
  • T-Lymphocytes, Cytotoxic