Mahapatra S, Ghosh T, Adhya S
Genetic Engineering Laboratory, Indian Institute of Chemical Biology, Calcutta.
Nucleic Acids Res. 1994 Aug 25;22(16):3381-6. doi: 10.1093/nar/22.16.3381.
Using an in vitro ribonuclease protection assay, it was shown that synthetic antisense transcripts from the 5'-upstream region of the beta-tubulin gene are efficiently imported into isolated Leishmania mitochondria. Import occurred after a lag of about 30 min at 25 degrees C and was dependent on ATP. Preincubation experiments suggested that import consists of a slow interaction of mitochondria with RNA, followed by rapid ATP-dependent uptake. Import was saturable with antisense RNA at about 1 nM concentration, and sequence-specific, as shown by lack of import of other labelled transcripts. Deletion analysis demonstrated a correlation between efficiency of import and the number of oligopurine motifs on the antisense RNA. Several small ribosomal RNAs (srRNAs) and Leishmania tRNA competed with antisense RNA for import. Incubation of mitochondria with srRNAs and tRNA in the presence of radiolabelled UTP resulted in the ribonuclease-resistant labelling of these RNAs by the mitochondrial terminal uridylyl transferase. Extracts of isolated mitochondria contain a factor binding to antisense RNA, as shown by gel retardation assay. These observations indicate the presence of a receptor-mediated import pathway for srRNAs and tRNA in Leishmania mitochondria.
通过体外核糖核酸酶保护试验表明,来自β-微管蛋白基因5'-上游区域的合成反义转录本可有效导入分离的利什曼原虫线粒体。在25℃下约30分钟的延迟后发生导入,且依赖于ATP。预孵育实验表明,导入包括线粒体与RNA的缓慢相互作用,随后是快速的ATP依赖摄取。反义RNA在约1 nM浓度时导入达到饱和,并且具有序列特异性,如其他标记转录本缺乏导入所示。缺失分析表明导入效率与反义RNA上寡嘌呤基序的数量之间存在相关性。几种小核糖体RNA(srRNA)和利什曼原虫tRNA与反义RNA竞争导入。在放射性标记的UTP存在下,将线粒体与srRNA和tRNA一起孵育,导致这些RNA被线粒体末端尿苷酰转移酶进行核糖核酸酶抗性标记。凝胶阻滞试验表明,分离线粒体的提取物中含有一种与反义RNA结合的因子。这些观察结果表明利什曼原虫线粒体中存在一种受体介导的srRNA和tRNA导入途径。