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首页> 外文期刊>Plant and cell physiology >The E-class PPR protein MEF3 of Arabidopsis thaliana can also function in mitochondrial RNA editing with an additional DYW domain.
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The E-class PPR protein MEF3 of Arabidopsis thaliana can also function in mitochondrial RNA editing with an additional DYW domain.

机译:拟南芥(Erabidopsis thaliana)的E类PPR蛋白MEF3还可以通过额外的DYW域在线粒体RNA编辑中发挥作用。

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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。我们在这里通过对生态类型Columbia(Col)和Landsberg erecta (L )之间的变异进行遗传作图来鉴定E域PPR亚类的PPR(五肽重复序列)蛋白MEF3(线粒体编辑因子3)线粒体中特定RNA编辑事件所需的拟南芥中的er )。 MEF3的L 变体与Col的不同之处在于重复序列9和10中的两个氨基酸,这使 atp4 -89位点的RNA编辑水平降低到L < 。在T-DNA插入线中,此站点上的编辑完全丢失。在 Vitis vinifera 中,与 MEF3 最相似的基因继续延伸到DYW延伸,超出了普通E结构域。用来自葡萄树和的PPR和E结构域的各种组合进行补充测定。拟南芥蛋白显示藤蔓E区可以代替 A。带有或不带有DYW结构域的拟南芥E区。这些发现表明,额外的DYW结构域不会干扰A中线粒体RNA编辑中的MEF3蛋白功能。拟南芥

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