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人类线粒体tRNA加工

Human mitochondrial tRNA processing.

作者信息

Rossmanith W, Tullo A, Potuschak T, Karwan R, Sbisà E

机构信息

Institut für Tumorbiologie-Krebsforschung, Universität Wien, Austria.

出版信息

J Biol Chem. 1995 May 26;270(21):12885-91. doi: 10.1074/jbc.270.21.12885.

Abstract

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.

摘要

转运RNA(tRNA)加工是哺乳动物线粒体基因表达中的核心事件。我们已经鉴定出参与HeLa细胞线粒体tRNA成熟的关键酶活性(核糖核酸酶P、前体tRNA 3'-内切核酸酶和ATP(CTP)-tRNA特异性核苷酸转移酶)。在同源线粒体体外加工系统中,不同的线粒体tRNA前体在tRNA的5'-和3'-末端被精确切割。5'-末端的切割先于3'-末端的切割,并且在同一体外系统中,tRNA是特异性添加CCA的底物。此外,通过比较酶学方法以及生化和免疫学技术,我们证明人类细胞含有两种不同的酶,它们从tRNA前体中去除5'-延伸,即先前表征的细胞核酶和新鉴定的线粒体核糖核酸酶P。这两种细胞同工酶具有不同的底物特异性,这似乎很好地适应了它们结构上不同的线粒体和细胞核tRNA底物。这种方法也可能有助于理解tRNA的结构多样性和共性。

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