An adenosine-to-inosine tRNA-editing enzyme that can perform C-to-U deamination of DNA

Proc Natl Acad Sci U S A. 2007 May 8;104(19):7821-6. doi: 10.1073/pnas.0702394104. Epub 2007 May 1.

Abstract

Adenosine-to-inosine editing in the anticodon of tRNAs is essential for viability. Enzymes mediating tRNA adenosine deamination in bacteria and yeast contain cytidine deaminase-conserved motifs, suggesting an evolutionary link between the two reactions. In trypanosomatids, tRNAs undergo both cytidine-to-uridine and adenosine-to-inosine editing, but the relationship between the two reactions is unclear. Here we show that down-regulation of the Trypanosoma brucei tRNA-editing enzyme by RNAi leads to a reduction in both C-to-U and A-to-I editing of tRNA in vivo. Surprisingly, in vitro, this enzyme can mediate A-to-I editing of tRNA and C-to-U deamination of ssDNA but not both in either substrate. The ability to use both DNA and RNA provides a model for a multispecificity editing enzyme. Notably, the ability of a single enzyme to perform two different deamination reactions also suggests that this enzyme still maintains specificities that would have been found in the ancestor deaminase, providing a first line of evidence for the evolution of editing deaminases.

MeSH terms

  • Adenosine / metabolism
  • Adenosine Deaminase / physiology*
  • Amino Acid Sequence
  • Base Sequence
  • Cell Line
  • Cytidine / metabolism
  • Cytidine Deaminase / physiology*
  • Deamination
  • Inosine / metabolism
  • Molecular Sequence Data
  • RNA Editing*
  • RNA Interference
  • Uridine / metabolism

Substances

  • Inosine
  • Cytidine
  • Adenosine Deaminase
  • Cytidine Deaminase
  • Adenosine
  • Uridine