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Discovery of new genes and deletion editing in Physarum mitochondria enabled by a novel algorithm for finding edited mRNAs

机译:发现新基因并删除线粒体中线粒体的新方法

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摘要

Gene finding is complicated in organisms that exhibit insertional RNA editing. Here, we demonstrate how our new algorithm Predictor of Insertional Editing (PIE) can be used to locate genes whose mRNAs are subjected to multiple frameshifting events, and extend the algorithm to include probabilistic predictions for sites of nucleotide insertion; this feature is particularly useful when designing primers for sequencing edited RNAs. Applying this algorithm, we successfully identified the nad2, nad4L, nad6 and atp8 genes within the mitochondrial genome of Physarum polycephalum, which had gone undetected by existing programs. Characterization of their mRNA products led to the unanticipated discovery of nucleotide deletion editing in Physarum. The deletion event, which results in the removal of three adjacent A residues, was confirmed by primer extension sequencing of total RNA. This finding is remarkable in that it comprises the first known instance of nucleotide deletion in this organelle, to be contrasted with nearly 500 sites of single and dinucleotide addition in characterized mitochondrial RNAs. Statistical analysis of this larger pool of editing sites indicates that there are significant biases in the 2 nt immediately upstream of editing sites, including a reduced incidence of nucleotide repeats, in addition to the previously identified purine-U bias.
机译:在具有插入RNA编辑功能的生物中,基因发现很复杂。在这里,我们演示了如何使用我们的新算法“插入编辑预测因子”(PIE)来定位其mRNA遭受多次移码事件的基因,并扩展该算法以包括核苷酸插入位点的概率预测;当设计用于对编辑的RNA进行测序的引物时,此功能特别有用。应用此算法,我们成功地鉴定了多头Phys草线粒体基因组中的nad2,nad4L,nad6和atp8基因,这些基因在现有程序中并未被发现。他们的mRNA产物的表征导致了意想不到的发现Physarum中核苷酸缺失编辑的发现。通过总RNA的引物延伸测序证实了导致三个相邻的A残基被去除的缺失事件。该发现是值得注意的,因为它包括该细胞器中核苷酸缺失的第一个已知实例,与特征性线粒体RNA中近500个单核苷酸和二核苷酸添加位点形成对比。对较大编辑位点池的统计分析表明,除了先前确定的嘌呤-U偏位以外,紧邻编辑位点上游的2 nt也存在明显的偏位,包括核苷酸重复的发生率降低。

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