In vivo studies of translational repression mediated by the granulocyte-macrophage colony-stimulating factor AU-rich element

J Biol Chem. 2004 Apr 2;279(14):13354-62. doi: 10.1074/jbc.M308003200. Epub 2004 Jan 15.

Abstract

The AU-rich element (ARE) controls the turnover of many unstable mRNAs and their translation. The granulocyte-macrophage colony-stimulating factor (GM-CSF) ARE is known to be a destabilizing element, but its role in translation remains unclear. Here we studied in vivo the role of the GM-CSF ARE on the mRNA and protein expressions of an enhanced green fluorescent protein reporter gene. The GM-CSF ARE had a repressor effect on translation independently of its effect on mRNA levels. In the context of an internal ribosome entry site, the GM-CSF ARE still repressed translation but was no longer functional as a destabilizing element. Gel retardation assays showed that poly(A)-binding protein is displaced from the poly(A) tail when the ARE is present in the 3'-untranslated region. These data suggest that the GM-CSF ARE controls translation and mRNA decay by interfering with poly(A)-binding protein-mediated mRNA circularization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Flow Cytometry
  • Genes, Reporter
  • Granulocyte-Macrophage Colony-Stimulating Factor / genetics*
  • Granulocyte-Macrophage Colony-Stimulating Factor / metabolism*
  • Green Fluorescent Proteins
  • HeLa Cells
  • Humans
  • Luminescent Proteins / genetics
  • Molecular Sequence Data
  • Protein Biosynthesis / physiology*
  • RNA, Messenger / genetics
  • Transfection

Substances

  • Luminescent Proteins
  • RNA, Messenger
  • Green Fluorescent Proteins
  • Granulocyte-Macrophage Colony-Stimulating Factor