Short double-stranded RNAs of specific sequence activate ribosomal TAK1-D and induce a global inhibition of translation

Biol Chem. 2009 May-Jun;390(5-6):453-62. doi: 10.1515/BC.2009.046.

Abstract

We have previously shown that short double-stranded RNAs of specific sequence induce phosphorylation in the activation loop of splicing variant D of the transforming growth factor beta-activated protein kinase 1 (TAK1-D). Here, we further characterize this novel function of TAK1-D and the mechanisms of this dsRNA-triggered phenomenon. Using a dominant negative TAK1-D mutant we demonstrate that TAK1-D activation is functionally required to trigger the activation of p38 MAP kinase and c-JUN terminal kinase and to induce cell death in NCI-H460 cells. While total TAK1-D protein was found in the cytoplasm as well as in the ribosomal fraction, activated TAK1-D phosphorylated on T184 and T187 in the activation loop was found to be exclusively associated with the 80S ribosome. The association of TAK1-D with the ribosome suggests an involvement in translation-dependent signaling and we demonstrate here that dsRNA-mediated activation of TAK1-D leads to a downregulation of mRNA translation. In addition, we show that TAK1-D is also phosphorylated after the induction of ribotoxic stress. Our data indicate that TAK1-D plays a role in the signaling events triggered by selected types of ribotoxic stress.

MeSH terms

  • Apoptosis
  • Cell Line, Tumor
  • Humans
  • Lung / cytology
  • MAP Kinase Kinase Kinases / analysis*
  • MAP Kinase Kinase Kinases / genetics
  • MAP Kinase Kinase Kinases / metabolism*
  • Mutagenesis, Site-Directed
  • Phosphorylation
  • Protein Biosynthesis
  • RNA, Double-Stranded / chemistry
  • RNA, Double-Stranded / metabolism*
  • Ribosome Subunits, Large, Eukaryotic
  • Ribosomes / chemistry
  • Ribosomes / genetics
  • Ribosomes / metabolism*

Substances

  • RNA, Double-Stranded
  • MAP Kinase Kinase Kinases
  • MAP kinase kinase kinase 7