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Intron RNA editing is essential for splicing in plant mitochondria

机译:内含子RNA编辑对于植物线粒体的剪接至关重要

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Most plant mitochondria messenger RNAs (mRNAs) undergo editing through C-to-U conversions located mainly in exon sequences. However, some RNA editing events are found in non-coding regions at critical positions in the predicted secondary and tertiary structures of introns, suggesting that RNA editing could be important for splicing. Here, we studied the relationships between editing and splicing of the mRNA encoding the ribosomal protein S10 (rps10), which has a group II intron and five editing sites. Two of them, C2 and C3, predicted to stabilize the folded structure of the intron necessary for splicing, were studied by using rps10 mutants introduced into isolated potato mitochondria by electroporation. While mutations of C2 involved in EBS2/IBS2 interactions did not affect splicing, probably by the presence of an alternative EBS2' region in domain I of the intron, the edition of site C3 turned out to be critical for rps10 mRNA splicing; only the edited (U) form of the transcript was processed. Interestingly, RNA editing was strongly reduced in transcripts from two different intronless genes, rps10 from potato and cox2 from wheat, suggesting that efficient RNA processing may require a close interaction of factors engaged in different maturation processes. This is the first report linking editing and splicing in conditions close to the in vivo situation.
机译:大多数植物线粒体信使RNA(mRNA)通过主要位于外显子序列中的C到U转换进行编辑。但是,在预测的内含子二级和三级结构中关键位置的非编码区域中发现了一些RNA编辑事件,这表明RNA编辑对于剪接可能很重要。在这里,我们研究了编码核糖体蛋白S10(rps10)的mRNA的编辑与剪接之间的关系,该蛋白具有第二组内含子和五个编辑位点。通过使用通过电穿孔引入分离的马铃薯线粒体中的rps10突变体,研究了其中的两个预测为稳定拼接所需内含子折叠结构的C2和C3。尽管参与EBS2 / IBS2相互作用的C2突变不影响剪接,可能是由于内含子I域中存在另一个EBS2'区域,但事实证明,C3版对于rps10 mRNA剪接至关重要。仅处理了已编辑(U)的成绩单形式。有趣的是,来自两个不同无内含子基因的转录本中的RNA编辑被大大降低,来自马铃薯的rps10和来自小麦的cox2,这表明有效的RNA加工可能需要参与不同成熟过程的因子的紧密相互作用。这是在接近体内情况的条件下将编辑和拼接联系起来的第一份报告。

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