Key result
Ablation of ATOM core subunits reduced mitochondrial tRNA levels by 60% to 75% in Trypanosoma brucei, indicating that tRNAs and proteins use the same import channel across the mitochondrial outer membrane.
In trypanosomes, tRNAs and proteins use the same outer membrane import pore (ATOM40), but tRNA import does not require protein import receptors.
Has no immediate clinical application; extends basic understanding of mitochondrial import mechanisms while leaving open whether similar shared pathways.
in vivo import of tRNAs requires four subunits of the mitochondrial outer membrane protein translocase but not the two receptor subunits, one of which is essential for protein import. The latter shows that it is possible to uncouple mitochondrial tRNA import from protein import. Ablation of the intermembrane space domain of the translocase subunit, archaic translocase of the outer membrane (ATOM)14, on the other hand, while not affecting the architecture of the translocase, impedes both protein and tRNA import. A protein import intermediate arrested in the translocation channel prevents both protein and tRNA import. In the presence of tRNA, blocking events of single-channel currents through the pore formed by recombinant ATOM40 were detected in electrophysiological recordings. These results indicate that both types of macromolecules use the same import channel across the outer membrane. However, while tRNA import depends on the core subunits of the protein import translocase, it does not require the protein import receptors, indicating that the two processes are not mechanistically linked.
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Niemann et al. (2017) studied this question. Ablation of ATOM core subunits vs. Uninduced cells (wild-type ATOM expression) was evaluated on Mitochondrial tRNA steady-state levels. Ablation of ATOM core subunits reduced mitochondrial tRNA levels by 60% to 75% in Trypanosoma brucei, indicating that tRNAs and proteins use the same import channel across the mitochondrial outer membrane.
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