Ubiquitin-dependent protein processing controls radiation-induced apoptosis through the N-end rule pathway

Exp Cell Res. 2000 May 25;257(1):48-57. doi: 10.1006/excr.2000.4870.

Abstract

The ubiquitination of nuclear proteins activated in human lymphocytes undergoing radiation-induced apoptosis and the subsequent downstream proteasomal protein processing, shown to be involved in apoptotic death control, may be dependent on an amino-terminal sequence identity of ubiquitin target proteins, the "N-end rule" pathway. Here we report that this selective pathway controls radiation-induced apoptosis and that it is involved in the initiation of this type of cell death. Dipeptide competitors of protein ubiquitination/processing dependent solely on the basic amino-terminal residues (type I) efficiently inhibited the radiation-induced apoptotic death phenotype, indicating that only the substrates of ubiquitination with basic NH2-terminal amino acids are involved in apoptotic death control. This selective inhibition was followed by an early, overall but also target-specific inhibition of ubiquitination and by an activation and stabilization of poly(ADP-ribose) polymerase (PARP) that occurs through inhibition of ubiquitination of its cleaved form (85 kDa). Interestingly, caspases-3 and -7 were not activated following irradiation, further suggesting that PARP cleavage may be regulated by an N-end rule pathway in a caspase-independent manner. These results highly suggest involvement of this subset of the ubiquitin system in the apoptotic death control and in the specific regulation of PARP activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids
  • Apoptosis / physiology*
  • Apoptosis / radiation effects
  • Cells, Cultured
  • Humans
  • Lymphocytes / pathology*
  • Lymphocytes / physiology*
  • Lymphocytes / radiation effects
  • Peptide Fragments
  • Poly(ADP-ribose) Polymerases / physiology*
  • Ubiquitins / physiology*

Substances

  • Amino Acids
  • Peptide Fragments
  • Ubiquitins
  • Poly(ADP-ribose) Polymerases