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The E-Class PPR Protein MEF3 of Arabidopsis thaliana Can Also Function in Mitochondrial RNA Editing With an Additional DYWn Domain

机译:拟南芥的E类PPR蛋白MEF3也可以通过附加的DYWn域在线粒体RNA编辑中起作用

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摘要

In plants, RNA editing is observed in mitochondria and plastids, changing selected C nucleotides into Us in both organelles. We here identify the PPR (pentatricopeptide repeat) protein MEF3 (mitochondrial editing factor 3) of the E domain PPR subclass by genetic mapping of a variation between ecotypes Columbia (Col) and Landsberg erecta (Ler) in Arabidopsis thaliana to be required for a specific RNA editing event in mitochondria. The Ler variant of MEF3 differs from Col in two amino acids in repeats 9 and 10, which reduce RNA editing levels at site atp4-89 to about 50% in Ler. In a T-DNA insertion line, editing at this site is completely lost. In Vitis vinifera the gene most similar to MEF3 continues into a DYW extension beyond the common E domain. Complementation assays with various combinations of PPR and E domains from the vine and A. thaliana proteins show that the vine E region can substitute for the A. thaliana E region with or without the DYW domain. These findings suggest that the additional DYW domain does not disturb the MEF3 protein function in mitochondrial RNA editing in A. thaliana.
机译:在植物中,在线粒体和质体中观察到RNA编辑,从而在两个细胞器中将选定的C核苷酸变为Us。我们在这里通过拟南芥中拟南芥生态类型Columbia(Col)和Landsberg erecta(Ler)之间的变异的遗传作图来鉴定E结构域PPR亚类的PPR(五肽重复序列)蛋白MEF3(线粒体编辑因子3)线粒体中的RNA编辑事件。 MEF3的Ler变体与Col的重复序列9和10中的两个氨基酸不同,这将Ler中atp4-89位点的RNA编辑水平降低至大约50%。在T-DNA插入线中,此站点上的编辑完全丢失。在葡萄中,与MEF3最相似的基因继续延伸到DYW延伸,超出了普通的E结构域。用来自葡萄和拟南芥蛋白质的PPR和E结构域的各种组合的互补测定法显示,具有或不具有DYW结构域的拟南芥E区域可以用藤蔓E区代替。这些发现表明,额外的DYW结构域不会干扰拟南芥线粒体RNA编辑中的MEF3蛋白功能。

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