HUMAN MITOCHONDRIAL TRANSFER-RNA PROCESSING

被引:131
作者
ROSSMANITH, W
TULLO, A
POTUSCHAK, T
KARWAN, R
SBISA, E
机构
[1] UNIV VIENNA, INST TUMORBIOL KREBSFORSCH, A-1010 VIENNA, AUSTRIA
[2] CNR, CTR STUDIO MITOCONDRI & METAB ENERGET, I-70126 BARI, ITALY
关键词
D O I
10.1074/jbc.270.21.12885
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
tRNA processing is a central event in mammalian mitochondrial gene expression. We have identified key enzymatic activities (ribonuclease P, precursor tRNA 3'-endonuclease, and ATP(CTP)-tRNA-specific nucleotidyltransferase) that are involved in HeLa cell mitochondrial tRNA maturation. Different mitochondrial tRNA precursors are cleaved precisely at the tRNA 5'- and 3'-ends in a homologous mitochondrial in vitro processing system, The cleavage at the 5'-end precedes that at the 3'-end, and the tRNAs are substrates for the specific CCA addition in the same in vitro system, Using a comparative enzymatic approach as well as biochemical and immunological techniques, we furthermore demonstrate that human cells contain two distinct enzymes that remove 5'-extensions from tRNA precursors, the previously characterized nuclear and the newly identified mitochondrial ribonuclease P. These two cellular isoenzymes have different substrate specificities that seem to be well adapted to their structurally disparate mitochondrial and nuclear tRNA substrates. This kind of approach may also help to understand the structural diversities and commonalities of tRNAs.
引用
收藏
页码:12885 / 12891
页数:7
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