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首页> 外文期刊>The Plant Cell >RNA PROCESSING FACTOR2 Is Required for 5' End Processing of nad9 and cox3 mRNAs in Mitochondria of Arabidopsis thaliana.
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RNA PROCESSING FACTOR2 Is Required for 5' End Processing of nad9 and cox3 mRNAs in Mitochondria of Arabidopsis thaliana.

机译:RNA处理因子2是拟南芥线粒体中nad9和cox3 mRNA 5'末端加工所必需的。

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摘要

In mitochondria of higher plants, the majority of 5' termini of mature mRNAs are generated posttranscriptionally. To gain insight into this process, we analyzed a natural 5' end polymorphism in the species Arabidopsis thaliana. This genetic approach identified the nuclear gene At1g62670, encoding a pentatricopeptide repeat protein. The functional importance of this mitochondrial restorer of fertility-like protein, designated RNA PROCESSING FACTOR2 (RPF2), is confirmed by the analysis of a respective T-DNA knockout mutant and its functional restoration by in vivo complementation. RPF2 fulfills two functions: it is required for the generation of a distinct 5' terminus of transcripts of subunit 9 of the NADH DEHYDROGENASE complex (nad9) and it determines the efficiency of 5' end formation of the mRNAs for subunit 3 of the CYTOCHROME C OXIDASE (cox3), the latter also being influenced by mitochondrial DNA sequences. Accordingly, recombinant RPF2 protein directly binds to a nad9 mRNA fragment in vitro. Two-dimensional gel electrophoresis and immunodetection analyses reveal that altered 5' processing does not influence accumulation of the nad9 and cox3 polypeptides. In accessions C24, Oystese-1, and Yosemite-0, different inactive RPF2 alleles exist, demonstrating the variability of this gene in ARABIDOPSIS: The identification of RPF2 is a major step toward the characterization of 5' mRNA processing in mitochondria of higher plants.
机译:在高等植物的线粒体中,大多数成熟mRNA的5'末端在转录后产生。为了深入了解这一过程,我们分析了拟南芥中的天然5'末端多态性。这种遗传方法确定了编码五碳肽重复蛋白的核基因At1g62670。通过分析相应的T-DNA敲除突变体及其通过体内互补的功能恢复,证实了这种育性样蛋白的线粒体恢复子的功能重要性,即RNA处理因子2(RPF2)。 RPF2具有两个功能:NADH脱氢酶复合物(nad9)9亚基的转录物独特的5'末端生成是必需的,并且它决定了CYTOCHROME C亚基3的mRNA的5'末端形成效率。氧化酶(cox3),后者也受线粒体DNA序列的影响。因此,重组RPF2蛋白在体外直接与nad9 mRNA片段结合。二维凝胶电泳和免疫检测分析表明,改变的5'加工过程不会影响nad9和cox3多肽的积累。在保藏号C24,Oystese-1和Yosemite-0中,存在不同的无活性RPF2等位基因,证明了该基因在ARABIDOPSIS中的变异性:RPF2的鉴定是表征高等植物线粒体5'mRNA加工的重要步骤。

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