Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation

Cell Metab. 2011 Sep 7;14(3):428-34. doi: 10.1016/j.cmet.2011.07.010.

Abstract

The metazoan mitochondrial translation machinery is unusual in having a single tRNA(Met) that fulfills the dual role of the initiator and elongator tRNA(Met). A portion of the Met-tRNA(Met) pool is formylated by mitochondrial methionyl-tRNA formyltransferase (MTFMT) to generate N-formylmethionine-tRNA(Met) (fMet-tRNA(met)), which is used for translation initiation; however, the requirement of formylation for initiation in human mitochondria is still under debate. Using targeted sequencing of the mtDNA and nuclear exons encoding the mitochondrial proteome (MitoExome), we identified compound heterozygous mutations in MTFMT in two unrelated children presenting with Leigh syndrome and combined OXPHOS deficiency. Patient fibroblasts exhibit severe defects in mitochondrial translation that can be rescued by exogenous expression of MTFMT. Furthermore, patient fibroblasts have dramatically reduced fMet-tRNA(Met) levels and an abnormal formylation profile of mitochondrially translated COX1. Our findings demonstrate that MTFMT is critical for efficient human mitochondrial translation and reveal a human disorder of Met-tRNA(Met) formylation.

Publication types

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

MeSH terms

  • Cells, Cultured
  • Child
  • Cyclooxygenase 1 / genetics
  • Cyclooxygenase 1 / metabolism*
  • DNA, Mitochondrial / chemistry*
  • DNA, Mitochondrial / genetics
  • Fibroblasts / metabolism*
  • Fibroblasts / pathology
  • Heterozygote
  • Humans
  • Hydroxymethyl and Formyl Transferases
  • Immunoblotting
  • Leigh Disease / genetics*
  • Leigh Disease / metabolism
  • Leigh Disease / pathology
  • Lentivirus
  • Mitochondria / genetics*
  • Mitochondria / metabolism
  • Mitochondrial Proteins / genetics*
  • Mitochondrial Proteins / metabolism
  • Mutation
  • Protein Biosynthesis* / genetics
  • RNA, Transfer, Met / metabolism*
  • Sequence Analysis, DNA
  • Transduction, Genetic
  • Virion

Substances

  • DNA, Mitochondrial
  • Mitochondrial Proteins
  • RNA, Transfer, Met
  • tRNA, formylmethionine-
  • Cyclooxygenase 1
  • PTGS1 protein, human
  • Hydroxymethyl and Formyl Transferases
  • methionyl-tRNA formyltransferase