Regulation of polyamine metabolism by translational control

Amino Acids. 2012 Feb;42(2-3):611-7. doi: 10.1007/s00726-011-1036-6. Epub 2011 Aug 3.

Abstract

Polyamines are low molecular weight, positively charged compounds that are ubiquitous in all living cells. They play a crucial role in many biochemical processes including regulation of transcription and translation, modulation of enzyme activities, regulation of ion channels and apoptosis. A strict balance between synthesis, catabolism and excretion tightly controls the cellular concentration of polyamines. The concentrations of rate-limiting enzymes in the polyamine synthesis and degradation pathways are regulated at different levels, including transcription, translation and degradation. Polyamines can modulate the translation of most of the enzymes required for their synthesis and catabolism through feedback mechanisms that are unique for each enzyme. Translational control is associated with cis-acting and trans-acting factors that can be influenced by the concentration of polyamines through mechanisms that are not completely understood. In this review, we present an overview of the translational control mechanisms of the proteins in the polyamine pathway, including ornithine decarboxylase (ODC), ODC antizyme, S-adenosylmethionine decarboxylase and spermidine/spermine N(1) acetyltransferase, highlighting the areas where more research is needed. A better understanding of the translational control of these enzymes would offer the possibility of a novel pharmacological intervention against cancer and other diseases.

Publication types

  • Review

MeSH terms

  • Acetyltransferases / metabolism
  • Adenosylmethionine Decarboxylase / metabolism
  • Animals
  • Biogenic Polyamines / metabolism*
  • Humans
  • Ornithine Decarboxylase / metabolism
  • Protein Biosynthesis*
  • Proteins / metabolism

Substances

  • Biogenic Polyamines
  • Proteins
  • ornithine decarboxylase antizyme
  • Acetyltransferases
  • diamine N-acetyltransferase
  • Ornithine Decarboxylase
  • Adenosylmethionine Decarboxylase