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Electroporation of DNA into Physarum polycephalum Mitochondria: Effects on Transcription and RNA Editing in Isolated Organelles

机译:DNA电穿孔入多头Phys线粒体:对转录和孤立的细胞器中的RNA编辑的影响。

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摘要

Mitochondrial RNAs in the acellular slime mold Physarum polycephalum contain nucleotides that are not encoded in the mitochondrial genes from which they are transcribed. These site-specific changes are quite extensive, comprising ~4% of the residues within mRNAs and ~2% of rRNAs and tRNAs. These “extra” nucleotides are added co-transcriptionally, but the means by which this is accomplished have not been elucidated. The cox1 mRNA also contains four sites of C to U changes, which occur post-transcriptionally, most likely via targeted deamination. The currently available in vitro systems for studying P. polycephalum editing are limited in that the template is the entire ~63,000 bp mitochondrial genome. This presents a significant challenge when trying to define the signals that specify editing sites. In an attempt to overcome this issue, a method for introducing DNA into isolated P. polycephalum mitochondria via electroporation has been developed. Exogenous DNA is expressed, but the transcripts synthesized from these templates are not edited under the conditions tested. However, transcripts derived from the mitochondrial genome are accurately edited after electroporation, indicating that the editing machinery is still functional. These findings suggest that this method may ultimately provide a feasible approach to elucidating editing signals.
机译:脱细胞粘液霉菌cephal头中的线粒体RNA包含未转录的线粒体基因中编码的核苷酸。这些位点特异性变化非常广泛,包括mRNA中约4%的残基以及rRNA和tRNA的约2%。这些“额外的”核苷酸是通过共转录方式添加的,但尚未阐明实现此目的的手段。 cox1 mRNA还包含从C到U变化的四个位点,这些位点在转录后发生,最有可能是通过靶向脱氨作用而发生的。目前用于研究多头假单胞菌编辑的体外系统受到限制,因为模板是整个〜63,000 bp的线粒体基因组。当试图定义指定编辑站点的信号时,这提出了巨大的挑战。为了克服这个问题,已经开发了一种通过电穿孔将DNA引入分离的多头疟原虫线粒体的方法。表达了外源DNA,但是从这些模板合成的转录本在测试条件下不被编辑。但是,从线粒体基因组中获得的转录本在电穿孔后可以得到准确的编辑,表明该编辑工具仍在起作用。这些发现表明,该方法最终可以为阐明编辑信号提供一种可行的方法。

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