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Accurate and efficient insertional RNA editing in isolated Physarum mitochondria.

机译:在分离的efficient线粒体中进行准确有效的插入RNA编辑。

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摘要

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.
机译:RNA编辑是一个过程,在该过程中核苷酸插入,缺失或碱基取代导致产生序列与其模板序列不同的RNA。多头Phys麦的线粒体RNA通过单核苷酸和二核苷酸插入以及明显的胞苷(C)到尿苷(U)的变化在多个位点进行特异性加工。这些处理事件的确切机制和时间安排目前未知。我们在这里描述了一种分离的线粒体系统的开发,其中可以在限定条件下将外源提供的核苷酸掺入RNAs中。 S1核酸酶保护,最近邻和RNase T1指纹分析的结果表明,这些新合成的线粒体RNA的绝大多数已通过单核苷酸和二核苷酸插入而被准确有效地处理。这项工作直接证明了在线粒体编辑系统中忠实核苷酸的插入。相反,新合成的RNA在分离的线粒体中未被C到U的变化处理,这表明在Physarum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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