Selective importation of RNA into isolated mitochondria from Leishmania tarentolae

• Published in: RNA (Cambridge) 2000-07, Vol.6 (7), p.988-1003, Article S1355838200991519
• Main Authors: RUBIO, MARY ANNE T., LIU, XUAN, YUZAWA, HARUMI, ALFONZO, JUAN D., SIMPSON, LARRY
• Format: Article
• Language: English
• Subjects: Adenosine Triphosphate - metabolism; Animals; Base Sequence; Binding, Competitive - drug effects; Digitonin - pharmacology; Dose-Response Relationship, Drug; Endopeptidase K - pharmacology; Enzyme Inhibitors - pharmacology; Indicators and Reagents - pharmacology; Kinetics; Leishmania - genetics; Leishmania - metabolism; Leishmania tarentolae; Membrane Potentials - drug effects; Micrococcal Nuclease - pharmacology; Mitochondria - drug effects; Mitochondria - genetics; Mitochondria - metabolism; Molecular Sequence Data; Oligomycins - pharmacology; ribonuclease P; RNA, Transfer - drug effects; RNA, Transfer - metabolism; RNA, Transfer, Gln - metabolism; RNA, Transfer, Ile - metabolism; Sodium Dodecyl Sulfate - pharmacology; Surface-Active Agents - pharmacology; Transcription, Genetic; tRNA Asp; tRNA Gln; tRNA Ile
• ISSN: 1355-8382; 1469-9001
• DOI: 10.1017/S1355838200991519

All mitochondrial tRNAs in kinetoplastid protozoa are encoded in the nucleus and imported from the cytosol. Incubation of two in vitro-transcribed tRNAs, tRNAIle(UAU) and tRNAGln(CUG), with isolated mitochondria from Leishmania tarentolae, in the absence of any added cytosolic fraction, resulted in a protease-sensitive, ATP-dependent importation, as measured by nuclease protection. Evidence that nuclease protection represents importation was obtained by the finding that Bacillus subtilis pre-tRNAAsp was protected from nuclease digestion and was also cleaved by an intramitochondrial RNase P-like activity to produce the mature tRNA. The presence of a membrane potential is not required for in vitro importation. A variety of small synthetic RNAs were also found to be efficiently imported in vitro. The data suggest that there is a structural requirement for importation of RNAs greater than ∼17 nt, and that smaller RNAs are apparently nonspecifically imported. The signals for importation of folded RNAs have not been determined, but the specificity of the process was illustrated by the higher saturation level of importation of the mainly mitochondria-localized tRNAIle as compared to the level of importation of the mainly cytosol-localized tRNAGln. Furthermore, exchanging the D-arm between the tRNAIle and the tRNAGln resulted in a reversal of the in vitro importation behavior and this could also be interpreted in terms of tertiary structure specificity.