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反向遗传学筛选鉴定了五个 E 类 PPR 蛋白,它们参与拟南芥线粒体中的 RNA 编辑。

Reverse genetic screening identifies five E-class PPR proteins involved in RNA editing in mitochondria of Arabidopsis thaliana.

机构信息

Molekulare Botanik, Universität Ulm, 89069 Ulm, Germany.

Molekulare Botanik, Universität Ulm, 89069 Ulm, Germany.

出版信息

J Biol Chem. 2010 Aug 27;285(35):27122-27129. doi: 10.1074/jbc.M110.128611. Epub 2010 Jun 21.

Abstract

RNA editing in flowering plant mitochondria post-transcriptionally alters several hundred nucleotides from C to U, mostly in mRNAs. Several factors required for specific RNA-editing events in plant mitochondria and plastids have been identified, all of them PPR proteins of the PLS subclass with a C-terminal E-domain and about half also with an additional DYW domain. Based on this information, we here probe the connection between E-PPR proteins and RNA editing in plant mitochondria. We initiated a reverse genetics screen of T-DNA insertion lines in Arabidopsis thaliana and investigated 58 of the 150 E-PPR-coding genes for a function in RNA editing. Six genes were identified to be involved in mitochondrial RNA editing at specific sites. Homozygous mutants of the five genes MEF18-MEF22 display no gross disturbance in their growth or development patterns, suggesting that the editing sites affected are not crucial at least in the greenhouse. These results show that a considerable percentage of the E-PPR proteins are involved in the functional processing of site-specific RNA editing in plant mitochondria.

摘要

在开花植物的线粒体中转录后 RNA 编辑将数百个核苷酸从 C 改变为 U,主要发生在 mRNA 中。已经鉴定出几种植物线粒体和质体中特定 RNA 编辑事件所需的因素,它们都是 PLS 亚类的 PPR 蛋白,具有 C 末端 E 结构域,大约一半还具有额外的 DYW 结构域。基于这些信息,我们在这里探讨 E-PPR 蛋白与植物线粒体中 RNA 编辑之间的联系。我们在拟南芥中启动了 T-DNA 插入系的反向遗传学筛选,并研究了 150 个 E-PPR 编码基因中的 58 个在特定位点的 RNA 编辑功能。确定了六个基因参与线粒体 RNA 编辑。MEF18-MEF22 这五个基因的纯合突变体在其生长或发育模式中没有明显的干扰,这表明受影响的编辑位点至少在温室中并不至关重要。这些结果表明,相当一部分 E-PPR 蛋白参与了植物线粒体中特定位点 RNA 编辑的功能处理。

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