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小麦线粒体提取物中转录RNA前体的加工

Processing of transfer RNA precursors in a wheat mitochondrial extract.

作者信息

Hanic-Joyce P J, Gray M W

机构信息

Department of Biochemistry, Dalhousie University, Halifax, Nova Scotia, Canada.

出版信息

J Biol Chem. 1990 Aug 15;265(23):13782-91.

PMID:1696257
Abstract

To investigate mechanisms for processing of plant mitochondrial RNAs, we studied the fate of wheat mitochondrial tRNA precursors in a homologous soluble extract. Artificial precursor transcripts were synthesized in vitro using T3 or T7 RNA polymerase and DNA templates containing wheat mitochondrial tRNA genes and flanking sequences. We found that the mitochondrial extract supports processing of precursors containing both native and chloroplast-like (Joyce, P. B. M., and Gray, M. W. (1989) Nucleic Acids Res. 77, 5461-5476) wheat mitochondrial tRNA sequences. Incubation of precursor transcripts with the extract results in processing of tRNAs via precise 5'- and 3'-endonucleolytic cleavages. However, these cleavages are not ordered in vitro because intermediates composed of 5'-leader + tRNA and tRNA + 3'-trailer are present simultaneously throughout the course of the reaction. Sequence analysis of processed products confirmed that endonucleolytic cleavages occur at the expected positions, generating tRNAs with 5'-phosphoryl and 3'-hydroxyl termini. The mitochondrial extract also contains a tRNA nucleotidyltransferase activity that adds -CCAOH termini to the 3'-ends of processed tRNAs. This cell-free RNA processing system provides the basis for biochemical characterization of the various enzymes involved in the production and maturation of plant mitochondrial tRNAs.

摘要

为了研究植物线粒体RNA的加工机制,我们在同源可溶性提取物中研究了小麦线粒体tRNA前体的命运。使用T3或T7 RNA聚合酶以及包含小麦线粒体tRNA基因和侧翼序列的DNA模板在体外合成人工前体转录本。我们发现线粒体提取物支持加工包含天然和叶绿体样(乔伊斯,P.B.M.,和格雷,M.W.(1989年)《核酸研究》77,5461 - 5476)小麦线粒体tRNA序列的前体。将前体转录本与提取物一起温育会通过精确的5'和3'内切核酸酶切割产生tRNA的加工产物。然而,这些切割在体外没有顺序,因为由5'前导序列 + tRNA和tRNA + 3'尾随序列组成的中间体在整个反应过程中同时存在。加工产物的序列分析证实内切核酸酶切割发生在预期位置,产生具有5'磷酸和3'羟基末端的tRNA。线粒体提取物还含有一种tRNA核苷酸转移酶活性,可将-CCAOH末端添加到加工后的tRNA的3'末端。这个无细胞RNA加工系统为参与植物线粒体tRNA产生和成熟的各种酶的生化特性研究提供了基础。

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