Demonstrates that tRNA and protein import into T. brucei mitochondria occur via distinct mechanisms.
Challenges assumptions of unified mitochondrial import; leaves open whether distinct tRNA pathways exist in mammalian cells or offer therapeutic targets.
Import of tRNA into the mitochondrial matrix of Trypanosoma brucei was reconstituted in vitro. Efficient import required the hydrolysis of externally added ATP and was shown to be a carrier-mediated process depending on proteinaceous receptors on the surface of mitochondria. A partly synthetic tRNA(Tyr) as well as a physiological tRNA(Lys) were imported along the same pathway. Contrary to import of all matrix-localized proteins, tRNA import does not require a membrane potential. Furthermore, addition of an excess of import-competent tRNA had no effect on import of a mitochondrial matrix protein. In summary, these results show that tRNAs and proteins in T. brucei are imported by fundamentally different mechanisms.
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Nabholz et al. (1999) studied this question.
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