Mutations in MTFMT Underlie a Human Disorder of Formylation Causing Impaired Mitochondrial Translation

• Published in: Cell metabolism Vol. 14; no. 3; pp. 428 - 434
• Main Authors: Tucker, Elena J., Hershman, Steven G., Köhrer, Caroline, Belcher-Timme, Casey A., Patel, Jinal, Goldberger, Olga A., Christodoulou, John, Silberstein, Jonathon M., McKenzie, Matthew, Ryan, Michael T., Compton, Alison G., Jaffe, Jacob D., Carr, Steven A., Calvo, Sarah E., RajBhandary, Uttam L., Thorburn, David R., Mootha, Vamsi K.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 07.09.2011
• Subjects: Animalia; Cells, Cultured; Child; children; Cyclooxygenase 1 - genetics; Cyclooxygenase 1 - metabolism; DNA, Mitochondrial - chemistry; DNA, Mitochondrial - genetics; exons; fibroblasts; Fibroblasts - metabolism; Fibroblasts - pathology; heterozygosity; Heterozygote; Humans; Hydroxymethyl and Formyl Transferases; Immunoblotting; Leigh Disease - genetics; Leigh Disease - metabolism; Leigh Disease - pathology; Lentivirus; mitochondria; Mitochondria - genetics; Mitochondria - metabolism; mitochondrial DNA; Mitochondrial Proteins - genetics; Mitochondrial Proteins - metabolism; Mutation; patients; Protein Biosynthesis - genetics; proteome; RNA, Transfer, Met - metabolism; Sequence Analysis, DNA; Transduction, Genetic; translation (genetics); Virion
• ISSN: 1550-4131; 1932-7420; 1932-7420
• DOI: 10.1016/j.cmet.2011.07.010

The metazoan mitochondrial translation machinery is unusual in having a single tRNAMet that fulfills the dual role of the initiator and elongator tRNAMet. A portion of the Met-tRNAMet pool is formylated by mitochondrial methionyl-tRNA formyltransferase (MTFMT) to generate N-formylmethionine-tRNAMet (fMet-tRNAmet), 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-tRNAMet 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-tRNAMet formylation. ► Mutations in MTFMT cause Leigh syndrome and combined OXPHOS deficiency ► Fibroblasts from patients with mutations in MTFMT have abnormal tRNAMet pools ► Met-tRNAMet formylation is critical for efficient human mitochondrial translation