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两种 RNA 编辑形式对于变形虫线粒体 tRNA 的成熟是必需的。

Two forms of RNA editing are required for tRNA maturation in Physarum mitochondria.

机构信息

Center for RNA Molecular Biology, Case Western Reserve University, 10900 Euclid Avenue, Cleveland, OH 44106, USA.

出版信息

RNA. 2010 Mar;16(3):482-8. doi: 10.1261/rna.1958810. Epub 2010 Jan 27.

Abstract

The mitochondrial genome of Physarum polycephalum encodes five tRNAs, four of which are edited by nucleotide insertion. Two of these tRNAs, tRNA(met1) and tRNA(met2), contain predicted mismatches at the beginning (proximal end) of the acceptor stem. In addition, the putative 5' end of tRNA(met2) overlaps the 3' end of a small, abundant, noncoding RNA, which we term ppoRNA. These anomalies led us to hypothesize that these two Physarum mitochondrial tRNAs undergo additional editing events. Here, we show that tRNA(met1) and tRNA(met2) each has a nonencoded G at its 5' end. In contrast to the other nucleotides that are added to Physarum mitochondrial RNAs, these extra G residues are likely added post-transcriptionally based on (1) the absence of added G in precursor transcripts containing inserted C and AA residues, (2) the presence of potential intermediates characteristic of 5' replacement editing, and (3) preferential incorporation of GTP into tRNA molecules under conditions that do not support transcription. This is the first report of both post-transcriptional nucleotide insertions and the addition of single Gs in P. polycephalum mitochondrial transcripts. We postulate that tRNA(met1) and tRNA(met2) are acted upon by an activity similar to that present in the mitochondria of certain other amoebozoons and chytrid fungi, suggesting that enzymes that repair the 5' end of tRNAs may be widespread.

摘要

多头绒泡菌的线粒体基因组编码了 5 个 tRNA,其中 4 个通过核苷酸插入进行编辑。这 5 个 tRNA 中的 2 个(tRNA(met1)和 tRNA(met2))在接受茎的起始(近端)处具有预测的错配。此外,tRNA(met2)的假定 5'端与一个小而丰富的非编码 RNA 的 3'端重叠,我们将其称为 ppoRNA。这些异常现象使我们假设这两个多头绒泡菌线粒体 tRNA 经历了额外的编辑事件。在这里,我们表明 tRNA(met1)和 tRNA(met2)在其 5'端都有一个非编码的 G。与添加到 Physarum 线粒体 RNA 的其他核苷酸不同,这些额外的 G 残基可能是基于以下原因添加的:(1) 在包含插入的 C 和 AA 残基的前体转录物中没有添加 G;(2) 存在 5' 替换编辑的特征中间产物;(3) 在不支持转录的条件下,GTP 优先掺入 tRNA 分子中。这是首次在多头绒泡菌线粒体转录物中报道了转录后核苷酸插入和单个 G 的添加。我们推测 tRNA(met1)和 tRNA(met2)受到类似于某些其他变形虫和壶菌线粒体中存在的活性的作用,这表明修复 tRNA 5' 端的酶可能广泛存在。

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