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Multiple specificity recognition motifs enhance plant mitochondrial RNA editing in vitro.多种特异性识别基序在体外增强植物线粒体RNA编辑
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2
Partially edited RNAs are intermediates of RNA editing in plant mitochondria.部分编辑的RNA是植物线粒体中RNA编辑的中间体。
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An in vitro RNA editing system from cauliflower mitochondria: editing site recognition parameters can vary in different plant species.来自花椰菜线粒体的体外RNA编辑系统:不同植物物种中编辑位点识别参数可能有所不同。
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4
RNA editing site recognition in heterologous plant mitochondria.异源植物线粒体中的RNA编辑位点识别
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RNA editing sites in plant mitochondria can share cis-elements.植物线粒体中的RNA编辑位点可以共享顺式元件。
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Recognition of RNA editing sites is directed by unique proteins in chloroplasts: biochemical identification of cis-acting elements and trans-acting factors involved in RNA editing in tobacco and pea chloroplasts.叶绿体中独特的蛋白质指导RNA编辑位点的识别:烟草和豌豆叶绿体中参与RNA编辑的顺式作用元件和反式作用因子的生化鉴定
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7
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Modeling sites of RNA editing as a fifth nucleotide state reveals progressive loss of edited sites from angiosperm mitochondria.将RNA编辑位点建模为第五种核苷酸状态揭示了被子植物线粒体中编辑位点的逐渐丧失。
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Different patterns in the recognition of editing sites in plant mitochondria.植物线粒体中编辑位点识别的不同模式。
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10
cis Recognition elements in plant mitochondrion RNA editing.植物线粒体RNA编辑中的顺式识别元件。
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Beyond a PPR-RNA recognition code: Many aspects matter for the multi-targeting properties of RNA editing factor PPR56.超越 PPR-RNA 识别码:许多因素影响 RNA 编辑因子 PPR56 的多靶向特性。
PLoS Genet. 2023 Aug 21;19(8):e1010733. doi: 10.1371/journal.pgen.1010733. eCollection 2023 Aug.
2
OTP970 Is Required for RNA Editing of Chloroplast Transcripts in .OTP970 对于. 中叶绿体转录本的 RNA 编辑是必需的。
Genes (Basel). 2022 Jan 14;13(1):139. doi: 10.3390/genes13010139.
3
High Level of Conservation of Mitochondrial RNA Editing Sites Among Four Species.四个物种中线粒体RNA编辑位点的高度保守性
G3 (Bethesda). 2019 Mar 7;9(3):709-717. doi: 10.1534/g3.118.200763.
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The longest mitochondrial RNA editing PPR protein MEF12 in Arabidopsis thaliana requires the full-length E domain.拟南芥中最长的线粒体RNA编辑PPR蛋白MEF12需要完整的E结构域。
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The RNA editing pattern of cox2 mRNA is affected by point mutations in plant mitochondria.cox2 mRNA 的 RNA 编辑模式受植物线粒体点突变的影响。
PLoS One. 2011;6(6):e20867. doi: 10.1371/journal.pone.0020867. Epub 2011 Jun 13.
6
A study of new Arabidopsis chloroplast RNA editing mutants reveals general features of editing factors and their target sites.一项关于新型拟南芥叶绿体 RNA 编辑突变体的研究揭示了编辑因子及其靶位点的一般特征。
Plant Cell. 2009 Nov;21(11):3686-99. doi: 10.1105/tpc.109.071472. Epub 2009 Nov 24.

本文引用的文献

1
The process of RNA editing in plant mitochondria.植物线粒体中的RNA编辑过程。
Mitochondrion. 2008 Jan;8(1):35-46. doi: 10.1016/j.mito.2007.09.004.
2
Cross-competition in editing of chloroplast RNA transcripts in vitro implicates sharing of trans-factors between different C targets.体外叶绿体RNA转录本编辑中的交叉竞争意味着不同C靶点之间反式作用因子的共享。
J Biol Chem. 2008 Mar 21;283(12):7314-9. doi: 10.1074/jbc.M709595200. Epub 2008 Jan 11.
3
Two RNA editing sites with cis-acting elements of moderate sequence identity are recognized by an identical site-recognition protein in tobacco chloroplasts.烟草叶绿体中具有中等序列同一性顺式作用元件的两个RNA编辑位点被同一种位点识别蛋白识别。
Nucleic Acids Res. 2008 Jan;36(1):311-8. doi: 10.1093/nar/gkm1026. Epub 2007 Nov 21.
4
RNA editing in plant mitochondria: assays and biochemical approaches.植物线粒体中的RNA编辑:分析方法与生化途径
Methods Enzymol. 2007;424:439-58. doi: 10.1016/S0076-6879(07)24020-0.
5
In vitro RNA editing in plant mitochondria does not require added energy.
FEBS Lett. 2007 Jun 12;581(14):2743-7. doi: 10.1016/j.febslet.2007.05.025. Epub 2007 May 21.
6
Conserved domain structure of pentatricopeptide repeat proteins involved in chloroplast RNA editing.参与叶绿体RNA编辑的五肽重复蛋白的保守结构域结构
Proc Natl Acad Sci U S A. 2007 May 8;104(19):8178-83. doi: 10.1073/pnas.0700865104. Epub 2007 May 2.
7
RNA editing site recognition in heterologous plant mitochondria.异源植物线粒体中的RNA编辑位点识别
Curr Genet. 2006 Dec;50(6):405-16. doi: 10.1007/s00294-006-0100-3. Epub 2006 Oct 11.
8
A pentatricopeptide repeat protein is a site recognition factor in chloroplast RNA editing.一个五肽重复序列蛋白是叶绿体RNA编辑中的位点识别因子。
J Biol Chem. 2006 Dec 8;281(49):37661-7. doi: 10.1074/jbc.M608184200. Epub 2006 Oct 2.
9
Mono- and dicotyledonous plant-specific RNA editing sites are correctly edited in both in organello systems.单子叶和双子叶植物特有的RNA编辑位点在两种细胞器系统中均被正确编辑。
FEBS Lett. 2006 Aug 7;580(18):4443-8. doi: 10.1016/j.febslet.2006.07.011. Epub 2006 Jul 14.
10
A simple in vitro RNA editing assay for chloroplast transcripts using fluorescent dideoxynucleotides: distinct types of sequence elements required for editing of ndh transcripts.一种使用荧光双脱氧核苷酸对叶绿体转录本进行体外RNA编辑的简单检测方法:ndh转录本编辑所需的不同类型序列元件
Plant J. 2006 Sep;47(5):802-10. doi: 10.1111/j.1365-313X.2006.02825.x. Epub 2006 Jul 11.

多种特异性识别基序在体外增强植物线粒体RNA编辑

Multiple specificity recognition motifs enhance plant mitochondrial RNA editing in vitro.

作者信息

Verbitskiy Daniil, van der Merwe Johannes A, Zehrmann Anja, Brennicke Axel, Takenaka Mizuki

机构信息

Institut für Molekulare Botanik, Universität Ulm, 89069 Ulm, Germany.

出版信息

J Biol Chem. 2008 Sep 5;283(36):24374-81. doi: 10.1074/jbc.M803292200. Epub 2008 Jul 1.

DOI:10.1074/jbc.M803292200
PMID:18596040
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3259818/
Abstract

Analysis of RNA editing in plant mitochondria has at least in vitro been hampered by very low activity. Consequently, none of the trans-acting factors involved has yet been identified. We here report that in vitro RNA editing increases dramatically when additional cognate recognition motifs are introduced into the template RNA molecule. Substrate RNAs with tandemly repeated recognition elements enhance in vitro RNA editing from 2-3% to 50-80%. The stimulation is not influenced by the editing status of a respective RNA editing site, suggesting that specific recognition of a site can be independent of the edited nucleotide itself. In vivo, attachment of the editing complex may thus be analogously initiated at sequence similarities in the vicinity of bona fide editing sites. This cis-acting enhancement decreases with increasing distance between the duplicated specificity signals; a cooperative effect is detectable up to approximately 200 nucleotides. Such repeated template constructs promise to be powerful tools for the RNA affinity identification of the as yet unknown trans-factors of plant mitochondrial RNA editing.

摘要

植物线粒体中RNA编辑的分析至少在体外受到极低活性的阻碍。因此,尚未鉴定出任何相关的反式作用因子。我们在此报告,当将额外的同源识别基序引入模板RNA分子时,体外RNA编辑会显著增加。具有串联重复识别元件的底物RNA可将体外RNA编辑从2%-3%提高到50%-80%。这种刺激不受相应RNA编辑位点编辑状态的影响,这表明对位点的特异性识别可能独立于被编辑的核苷酸本身。在体内,编辑复合体的附着可能因此类似地在真正编辑位点附近的序列相似性处启动。这种顺式作用增强随着重复特异性信号之间距离的增加而降低;在大约200个核苷酸范围内可检测到协同效应。这种重复模板构建体有望成为用于RNA亲和鉴定植物线粒体RNA编辑中尚未知的反式因子的强大工具。