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在分离的绒泡菌线粒体中进行准确且高效的插入式RNA编辑。

Accurate and efficient insertional RNA editing in isolated Physarum mitochondria.

作者信息

Visomirski-Robic L M, Gott J M

机构信息

Department of Molecular Biology and Microbiology, School of Medicine, Case Western Reserve University, Cleveland, Ohio 44106, USA.

出版信息

RNA. 1995 Sep;1(7):681-91.

Abstract

RNA editing is a process whereby nucleotide insertion, deletion, or base substitution results in the production of an RNA whose sequence differs from that of its template. The mitochondrial RNAs of Physarum polycephalum are processed specifically at multiple sites by both mono- and dinucleotide insertions, as well as apparent cytidine (C) to uridine (U) changes. The precise mechanism and timing of these processing events are currently unknown. We describe here the development of an isolated mitochondrial system in which exogenously supplied nucleotides can be incorporated into RNAs under defined conditions. The results of S1 nuclease protection, nearest neighbor and RNase T1 fingerprint analyses indicate that the vast majority of these newly synthesized mitochondrial RNAs have been accurately and efficiently processed by both mono- and dinucleotide insertions. This work provides a direct demonstration of faithful nucleotide insertion in a mitochondrial editing system. In contrast, the newly synthesized RNAs are not processed by C to U changes in the isolated mitochondria, suggesting that the base changes observed in Physarum are unlikely to occur via a deletion/insertion mechanism.

摘要

RNA编辑是一个核苷酸插入、缺失或碱基替换导致产生一种RNA的过程,该RNA的序列与其模板序列不同。多头绒泡菌的线粒体RNA在多个位点通过单核苷酸和双核苷酸插入以及明显的胞嘧啶(C)到尿嘧啶(U)的变化进行特异性加工。这些加工事件的确切机制和时间目前尚不清楚。我们在此描述了一种分离的线粒体系统的开发,在该系统中,外源性提供的核苷酸可以在特定条件下掺入RNA中。S1核酸酶保护、最近邻分析和核糖核酸酶T1指纹分析结果表明,这些新合成的线粒体RNA绝大多数已通过单核苷酸和双核苷酸插入被准确且高效地加工。这项工作直接证明了线粒体编辑系统中核苷酸的忠实插入。相比之下,新合成的RNA在分离的线粒体中不会通过C到U的变化进行加工,这表明在多头绒泡菌中观察到的碱基变化不太可能通过缺失/插入机制发生。

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