Defines translation initiation mechanisms for leaderless mRNA in human mitochondria, suggesting new insights into mitochondrial function.
Mitochondrial translation is essential for cellular function, and its dysregulation is associated with mitochondrial disorders and cancer. However, the mechanisms by which human mitochondrial ribosomes initiate translation remain poorly understood, particularly because mitochondrial mRNAs generally lack the 5′ untranslated regions that guide translation initiation in bacterial and cytoplasmic systems. Using real-time single-molecule fluorescence measurements, biochemical assays, and cryo-EM analysis, we show that human mitochondrial translation initiation occurs through two parallel pathways. In one pathway, leaderless mRNA first loads onto the 28S small subunit, followed by recruitment of the 39S large subunit to form the 55S initiation complex. In the second pathway, a preassembled 55S monosome directly loads onto leaderless mRNA. Both pathways require recruitment of mtIF2 and fMet-tRNAMet before mRNA binding. However, the monosome-loading pathway tolerates non-formylated Met-tRNAMet and is suppressed by mtIF3. Together, these findings define the heterogeneous pathways of human mitochondrial translation initiation on leaderless mRNAs. How human mitochondrial ribosomes initiate translation remains elusive. Here, the authors combined biochemical reconstitution, single-molecule fluorescence spectroscopy, and cryo-EM approaches to define the heterogeneous pathways of human mitochondrial leaderless mRNA translation initiation.
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Shen et al. (2026) studied this question.
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