Molecular basis of translation termination at noncanonical stop codons in human mitochondria

Research output: Contribution to journalJournal articleResearchpeer-review

  • Martin Saurer
  • Marc Leibundgut
  • Hima Priyanka Nadimpalli
  • Alain Scaiola
  • Tanja Schönhut
  • Richard G Lee
  • Stefan J Siira
  • Oliver Rackham
  • René Dreos
  • Tea Lenarčič
  • Kummer, Eva
  • David Gatfield
  • Aleksandra Filipovska
  • Nenad Ban

The genetic code that specifies the identity of amino acids incorporated into proteins during protein synthesis is almost universally conserved. Mitochondrial genomes feature deviations from the standard genetic code, including the reassignment of two arginine codons to stop codons. The protein required for translation termination at these noncanonical stop codons to release the newly synthesized polypeptides is not currently known. In this study, we used gene editing and ribosomal profiling in combination with cryo-electron microscopy to establish that mitochondrial release factor 1 (mtRF1) detects noncanonical stop codons in human mitochondria by a previously unknown mechanism of codon recognition. We discovered that binding of mtRF1 to the decoding center of the ribosome stabilizes a highly unusual conformation in the messenger RNA in which the ribosomal RNA participates in specific recognition of the noncanonical stop codons.

Original languageEnglish
Issue number6644
Pages (from-to)531-536
Number of pages6
Publication statusPublished - 2023

    Research areas

  • Humans, Codon, Terminator, Cryoelectron Microscopy, Peptide Termination Factors/chemistry, Protein Biosynthesis, Proteins/genetics, Mitochondria/genetics, Peptide Chain Termination, Translational

ID: 346587943