A natural non-Watson-Crick base pair in human mitochondrial tRNAThr causes structural and functional susceptibility to local mutations

Nucleic Acids Res. 2018 May 18;46(9):4662-4676. doi: 10.1093/nar/gky243.

Abstract

Six pathogenic mutations have been reported in human mitochondrial tRNAThr (hmtRNAThr); however, the pathogenic molecular mechanism remains unclear. Previously, we established an activity assay system for human mitochondrial threonyl-tRNA synthetase (hmThrRS). In the present study, we surveyed the structural and enzymatic effects of pathogenic mutations in hmtRNAThr and then focused on m.15915 G > A (G30A) and m.15923A > G (A38G). The harmful evolutionary gain of non-Watson-Crick base pair A29/C41 caused hmtRNAThr to be highly susceptible to mutations disrupting the G30-C40 base pair in various ways; for example, structural integrity maintenance, modification and aminoacylation of tRNAThr, and editing mischarged tRNAThr. A similar phenomenon was observed for hmtRNATrp with an A29/C41 non-Watson-Crick base pair, but not in bovine mtRNAThr with a natural G29-C41 base pair. The A38G mutation caused a severe reduction in Thr-acceptance and editing of hmThrRS. Importantly, A38 is a nucleotide determinant for the t6A modification at A37, which is essential for the coding properties of hmtRNAThr. In summary, our results revealed the crucial role of the G30-C40 base pair in maintaining the proper structure and function of hmtRNAThr because of A29/C41 non-Watson-Crick base pair and explained the molecular outcome of pathogenic G30A and A38G mutations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anticodon
  • Base Pairing
  • Humans
  • Mitochondria / enzymology
  • Mutation*
  • RNA Editing
  • RNA, Mitochondrial / chemistry*
  • RNA, Mitochondrial / genetics
  • RNA, Mitochondrial / metabolism
  • RNA, Transfer, Thr / chemistry*
  • RNA, Transfer, Thr / genetics
  • RNA, Transfer, Thr / metabolism
  • Threonine-tRNA Ligase / metabolism
  • Transfer RNA Aminoacylation

Substances

  • Anticodon
  • RNA, Mitochondrial
  • RNA, Transfer, Thr
  • Threonine-tRNA Ligase