Prevention of rapid intracellular degradation of ODC by a carboxyl-terminal truncation

Science. 1989 Mar 17;243(4897):1493-5. doi: 10.1126/science.2928784.

Abstract

Ornithine decarboxylase (ODC) was converted from a protein with a short intracellular half-life in mammalian cells to a stable protein by truncating 37 residues at its carboxyl terminus. Cells expressing wild-type protein lost ODC activity with a half-life of approximately 1 hour. Cells expressing the truncated protein, however, retained full activity for at least 4 hours. Pulse-chase experiments in which immunoprecipitation and gel electrophoresis were used confirmed the stabilizing effect of the truncation. Thus, a carboxyl-terminal domain is responsible for the rapid intracellular degradation of murine ODC.

Publication types

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

MeSH terms

  • Animals
  • Cell Line
  • Cloning, Molecular
  • Mice
  • Ornithine Decarboxylase / genetics
  • Ornithine Decarboxylase / metabolism*
  • Recombinant Proteins / metabolism
  • Structure-Activity Relationship
  • Transfection

Substances

  • Recombinant Proteins
  • Ornithine Decarboxylase