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Selective importation of RNA into isolated mitochondria from Leishmania tarentolae

Published online by Cambridge University Press:  01 July 2000

MARY ANNE T. RUBIO ,
XUAN LIU ,
HARUMI YUZAWA ,
JUAN D. ALFONZO  and
LARRY SIMPSON
MARY ANNE T. RUBIO
Affiliation:
Department of Microbiology, Immunology and Molecular Genetics, University of California, Los Angeles, School of Medicine, Los Angeles, California 90095, USA
XUAN LIU
Affiliation:
Howard Hughes Medical Institute, University of California, Los Angeles, School of Medicine, Los Angeles, California 90095, USA Current address: Osiris Therapeutics, Inc., 2001 Aliceanna Street, Baltimore, Maryland 21231, USA.
HARUMI YUZAWA
Affiliation:
Howard Hughes Medical Institute, University of California, Los Angeles, School of Medicine, Los Angeles, California 90095, USA Current address: Department of Bacteriology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-Ku, Tokyo 113-8421, Japan.
JUAN D. ALFONZO
Affiliation:
Department of Microbiology, Immunology and Molecular Genetics, University of California, Los Angeles, School of Medicine, Los Angeles, California 90095, USA
LARRY SIMPSON
Affiliation:
Department of Microbiology, Immunology and Molecular Genetics, University of California, Los Angeles, School of Medicine, Los Angeles, California 90095, USA Howard Hughes Medical Institute, University of California, Los Angeles, School of Medicine, Los Angeles, California 90095, USA
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Abstract

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.

Keywords

Leishmania tarentolaemitochondriaRNA importtRNA
Type
Research Article
Information
RNA , Volume 6 , Issue 7 , July 2000 , pp. 988 - 1003
Copyright
2000 RNA Society

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