An active role for the ribosome in determining the fate of oxidized mRNA

Cell Rep. 2014 Nov 20;9(4):1256-64. doi: 10.1016/j.celrep.2014.10.042. Epub 2014 Nov 13.

Abstract

Chemical damage to RNA affects its functional properties and thus may pose a significant hurdle to the translational apparatus; however, the effects of damaged mRNA on the speed and accuracy of the decoding process and their interplay with quality-control processes are not known. Here, we systematically explore the effects of oxidative damage on the decoding process using a well-defined bacterial in vitro translation system. We find that the oxidative lesion 8-oxoguanosine (8-oxoG) reduces the rate of peptide-bond formation by more than three orders of magnitude independent of its position within the codon. Interestingly, 8-oxoG had little effect on the fidelity of the selection process, suggesting that the modification stalls the translational machinery. Consistent with these findings, 8-oxoG mRNAs were observed to accumulate and associate with polyribosomes in yeast strains in which no-go decay is compromised. Our data provide compelling evidence that mRNA-surveillance mechanisms have evolved to cope with damaged mRNA.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Extracts
  • Guanosine / analogs & derivatives*
  • Guanosine / metabolism
  • Oxidation-Reduction
  • Peptides / metabolism
  • Polyribosomes / metabolism
  • Protein Biosynthesis
  • RNA Stability
  • RNA, Messenger / metabolism*
  • Ribosomes / metabolism*
  • Saccharomyces cerevisiae / metabolism

Substances

  • Cell Extracts
  • Peptides
  • RNA, Messenger
  • Guanosine
  • 8-hydroxyguanosine