The PAAD/PYRIN-only protein POP1/ASC2 is a modulator of ASC-mediated nuclear-factor-kappa B and pro-caspase-1 regulation

Biochem J. 2003 Jul 1;373(Pt 1):101-13. doi: 10.1042/BJ20030304.

Abstract

Proteins containing PAAD [pyrin, AIM (absent-in-melanoma), ASC [apoptosis-associated speck-like protein containing a CARD (caspase-recruitment domain)] and DD (death domain)-like] (PYRIN, DAPIN) domains are involved in innate immunity, regulating pathways leading to nuclear-factor-kappa B (NF-kappa B) and pro-caspase-1 activation. Many PAAD-family proteins have structures reminiscent of Nod-1, a putative intracellular sensor of lipopolysaccharide. Hereditary mutations in some of the PAAD-family genes are associated with auto-inflammatory diseases. Several of these proteins utilize the bipartite PAAD- and CARD-containing adapter protein ASC/TMS-1 (target of methylation-induced silencing) for linking to downstream signalling pathways. In the present paper, we describe characterization of human PAAD-only protein-1 (POP1)/ASC2, which is highly homologous with the PAAD domain of ASC, and which probably originated by gene duplication on chromosome 16. We demonstrate that POP1/ASC2 associates with ASC via PAAD-PAAD interactions and modulates NF-kappa B and pro-caspase-1 regulation by this adapter protein. In gene transfer experiments, POP1/ASC2 suppressed cytokine-mediated NF-kappa B activation similar to other PAAD-family proteins previously tested. Immunohistochemical studies showed expression of POP1/ASC2 predominantly in macrophages and granulocytes. We propose that POP1/ASC2 functions as a modulator of multidomain PAAD-containing proteins involved in NF-kappa B and pro-caspase-1 activation and innate immunity.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Apoptosis Regulatory Proteins
  • COS Cells
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Caspase 1
  • Caspases / metabolism*
  • Cell Line
  • Chlorocebus aethiops
  • Cloning, Molecular
  • Cytoskeletal Proteins
  • Enzyme Activation
  • Enzyme Precursors / metabolism*
  • Genes, Reporter
  • Humans
  • Luciferases / genetics
  • Molecular Sequence Data
  • NF-kappa B / metabolism*
  • Open Reading Frames
  • Polymerase Chain Reaction
  • Proteins / metabolism*
  • Pyrin
  • Recombinant Proteins / metabolism
  • Ribonucleoproteins / genetics
  • Ribonucleoproteins / metabolism*
  • Sequence Alignment
  • Sequence Homology, Amino Acid
  • Transfection

Substances

  • Apoptosis Regulatory Proteins
  • Carrier Proteins
  • Cytoskeletal Proteins
  • Enzyme Precursors
  • MEFV protein, human
  • NF-kappa B
  • POP1 protein, human
  • Proteins
  • Pyrin
  • Recombinant Proteins
  • Ribonucleoproteins
  • Luciferases
  • Caspases
  • Caspase 1