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      ICE-LAP3, a novel mammalian homologue of the Caenorhabditis elegans cell death protein Ced-3 is activated during Fas- and tumor necrosis factor-induced apoptosis.

      The Journal of Biological Chemistry
      Animals, Fetus, Caenorhabditis elegans Proteins, Apoptosis, Humans, Gene Expression, Antigens, CD95, Caspases, pharmacology, Rats, Tumor Cells, Cultured, Cysteine Endopeptidases, Caenorhabditis elegans, physiology, Adult, DNA Primers, Molecular Sequence Data, Helminth Proteins, Protein Precursors, Sequence Homology, Amino Acid, biosynthesis, Protein Biosynthesis, Tumor Necrosis Factor-alpha, Recombinant Proteins, Multigene Family, metabolism, Breast Neoplasms, Amino Acid Sequence, drug effects, Caspase 7, Polymerase Chain Reaction, Base Sequence, chemistry, Proteins, Cell Line, Female

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          Abstract

          Members of the ICE/ced-3 gene family have been implicated as components of the cell death pathway. Based on similarities with the structural prototype interleukin-1 beta-converting enzyme (ICE), family members are synthesized as proenzymes that are proteolytically processed to form active heterodimeric enzymes. In this report, we describe a novel member of this growing gene family, ICE-LAP3, which is closely related to the death effector Yama/CPP32/Apopain. Pro-ICE-LAP3 is a 35-kDa protein localized to the cytoplasm and expressed in a variety of tissues and cell lines. Overexpression of a truncated version of ICE-LAP3 (missing the pro-domain) induces apoptosis in MCF7 breast carcinoma cells. Importantly, upon receipt of a death stimulus, endogenous ICE-LAP3 is processed to its subunit forms, suggesting a physiological role in cell death. This is the first report to demonstrate processing of a native ICE/ced-3 family member during execution of the death program and the first description of the subcellular localization of an ICE/ced-3 family member.

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