Translational regulation of ornithine decarboxylase and other enzymes of the polyamine pathway

Int J Biochem Cell Biol. 1999 Jan;31(1):107-22. doi: 10.1016/s1357-2725(98)00135-6.

Abstract

It has long been known that polyamines play an essential role in the proliferation of mammalian cells, and the polyamine biosynthetic pathway may provide an important target for the development of agents that inhibit carcinogenesis and tumor growth. The rate-limiting enzymes of the polyamine pathway, ornithine decarboxylase (ODC) and S-adenosylmethionine decarboxylase (AdoMetDC), are highly regulated in the cell, and much of this regulation occurs at the level of translation. Although the 5' leader sequences of ODC and AdoMetDC are both highly structured and contain small internal open reading frames (ORFs), the regulation of their translation appears to be quite different. The translational regulation of ODC is more dependent on secondary structure, and therefore responds to the intracellular availability of active eIF-4E, the cap-binding subunit of the eIF-4F complex, which mediates translation initiations. Cell-specific translation of AdoMetDC appears to be regulated exclusively through the internal ORF, which causes ribosome stalling that is independent of eIF-4E levels and decreases the efficiency with which the downstream ORF encoding AdoMetDC protein is translated. The translation of both ODC and AdoMetDC is negatively regulated by intracellular changes in the polyamines spermidine and spermine. Thus, when polyamine levels are low, the synthesis of both ODC and AdoMetDC is increased, and an increase in polyamine content causes a corresponding decrease in protein synthesis. However, an increase in active eIF-4E may allow for the synthesis of ODC even in the presence of polyamine levels that repress ODC translation in cells with lower levels of the initiation factor. In contrast, the amino acid sequence that is encoded by the upstream ORF is critical for polyamine regulation of AdoMetDC synthesis and polyamines may affect synthesis by interaction with the putative peptide, MAGDIS.

Publication types

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

MeSH terms

  • Adenosylmethionine Decarboxylase / genetics
  • Adenosylmethionine Decarboxylase / metabolism
  • Animals
  • Enzymes / genetics
  • Enzymes / metabolism
  • Gene Expression Regulation
  • Humans
  • Ornithine Decarboxylase / chemistry
  • Ornithine Decarboxylase / genetics*
  • Ornithine Decarboxylase / metabolism*
  • Peptide Initiation Factors / genetics
  • Peptide Initiation Factors / metabolism
  • Polyamines / metabolism*
  • Protein Biosynthesis*
  • Spermidine / metabolism
  • Spermine / metabolism

Substances

  • Enzymes
  • Peptide Initiation Factors
  • Polyamines
  • Spermine
  • Ornithine Decarboxylase
  • Adenosylmethionine Decarboxylase
  • Spermidine