ICE-LAP6, a novel member of the ICE/Ced-3 gene family, is activated by the cytotoxic T cell protease granzyme B

J Biol Chem. 1996 Jul 12;271(28):16720-4. doi: 10.1074/jbc.271.28.16720.

Abstract

Members of the ICE/Ced-3 gene family are likely effector components of the cell death machinery. Here, we characterize a novel member of this family designated ICE-LAP6. By phylogenetic analysis, ICE-LAP6 is classified into the Ced-3 subfamily which includes Ced-3, Yama/CPP32/apopain, Mch2, and ICE-LAP3/Mch3/CMH-1. Interestingly, ICE-LAP6 contains an active site QACGG pentapeptide, rather than the QACRG pentapeptide shared by other family members. Overexpression of ICE-LAP6 induces apoptosis in MCF7 breast carcinoma cells. More importantly, ICE-LAP6 is proteolytically processed into an active cysteine protease by granzyme B, an important component of cytotoxic T cell-mediated apoptosis. Once activated, ICE-LAP6 is able to cleave the death substrate poly(ADP-ribose) polymerase into signature apoptotic fragments.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Apoptosis / genetics
  • Binding Sites
  • Caenorhabditis elegans Proteins
  • Caspase 1
  • Caspase 9
  • Caspases*
  • Cysteine Endopeptidases / genetics*
  • Cysteine Endopeptidases / metabolism
  • DNA, Complementary
  • Granzymes
  • Helminth Proteins / genetics*
  • Humans
  • Molecular Sequence Data
  • Sequence Homology, Amino Acid
  • Serine Endopeptidases / metabolism*
  • T-Lymphocytes, Cytotoxic / enzymology*
  • Tumor Cells, Cultured

Substances

  • Caenorhabditis elegans Proteins
  • DNA, Complementary
  • Helminth Proteins
  • GZMB protein, human
  • Granzymes
  • Serine Endopeptidases
  • CASP9 protein, human
  • Caspase 9
  • Caspases
  • Cysteine Endopeptidases
  • ced-3 protein, C elegans
  • Caspase 1

Associated data

  • GENBANK/U56390