Molekulare Botanik, Universität Ulm, 89069, Ulm, Germany.
Plant Mol Biol. 2013 Mar;81(4-5):337-46. doi: 10.1007/s11103-012-0003-2. Epub 2013 Jan 4.
A forwards genetic screen of a chemically mutated plant population identified mitochondrial RNA editing factor 10 (MEF10) in Arabidopsis thaliana. MEF10 is a trans-factor required specifically for the C to U editing of site nad2-842. The MEF10 protein is characterized by a stretch of pentatricopeptide repeats (PPR) and a C-terminal extension domain ending with the amino acids DYW. Editing is lost in mutant plants but is recovered by transgenic introduction of an intact MEF10 gene. The MEF10 protein interacts with multiple organellar RNA editing factor 8 (MORF8) but not with other mitochondrial MORF proteins in yeast two hybrid assays. These results support the model that specific combinations of MORF and MEF proteins are involved in RNA editing in plant mitochondria.
通过对化学诱变的植物群体进行正向遗传学筛选,在拟南芥中鉴定到线粒体 RNA 编辑因子 10(MEF10)。MEF10 是一种反式因子,特异性地参与nad2-842 位点的 C 到 U 编辑。MEF10 蛋白的特征是一段五肽重复序列(PPR)和一个 C 末端延伸结构域,末端是氨基酸 DYW。在突变体植物中,编辑丢失,但通过转基因引入完整的 MEF10 基因可以恢复。在酵母双杂交实验中,MEF10 蛋白与多个细胞器 RNA 编辑因子 8(MORF8)相互作用,但不与其他线粒体 MORF 蛋白相互作用。这些结果支持这样的模型,即特定的 MORF 和 MEF 蛋白组合参与植物线粒体中的 RNA 编辑。