利用人工合成的 P 型 PPR 编辑因子在植物细胞器中进行新的 RNA 碱基编辑

Sebastien Mathieu, Elena Lesch, Shahinez Garcia, Stefanie Graindorge, Mareike Schallenberg-Rudinger, Kamel Hammani
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引用次数: 0

摘要

在植物线粒体和叶绿体中,胞苷-尿苷 RNA 编辑在调节基因表达方面发挥着至关重要的作用。天然的 PLS 型 PPR 蛋白专门负责这一过程,而合成的 PPR 蛋白则为定向 RNA 编辑提供了巨大的潜力。在这项研究中,我们将合成的 P 型 PPR 引导蛋白与苔藓线粒体编辑因子 PPR56 的 DYW 胞苷脱氨酶结构域融合,从而设计出了嵌合编辑因子。这些设计PPR编辑因子(dPPRe)在大肠杆菌、烟草叶绿体和线粒体中引起了高效、精确的从头RNA编辑。对最有效的 dPPRe 进行的叶绿体转录组分析表明,脱靶效应极小,只有三个非目标 C 位点因与目标序列相似而被编辑。这项研究介绍了一种在植物细胞器中进行 RNA 碱基编辑的新颖而精确的方法,为适用于植物和其他潜在生物的基因调控新方法铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
De novo RNA base editing in plant organelles with engineered synthetic P-type PPR editing factors
In plant mitochondria and chloroplasts, cytidine-to-uridine RNA editing plays a crucial role in regulating gene expression. While natural PLS-type PPR proteins are specialized in this process, synthetic PPR proteins offer significant potential for targeted RNA editing. In this study, we engineered chimeric editing factors by fusing synthetic P-type PPR guides with the DYW cytidine deaminase domain of a moss mitochondrial editing factor, PPR56. These designer PPR editors (dPPRe) elicited efficient and precise de novo RNA editing in Escherichia coli, and in Nicotiana benthamiana chloroplasts and mitochondria. Chloroplast transcriptome-wide analysis of the most efficient dPPRe revealed minimal off-target effects, with only three non-target C sites edited due to sequence similarity with the intended target. This study introduces a novel and precise method for RNA base editing in plant organelles, paving the way for new approaches in gene regulation applicable to plants and potentially other organisms.
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