Molekulare Botanik, Universität Ulm, Ulm, Germany.
FEBS Lett. 2010 Oct 8;584(19):4181-6. doi: 10.1016/j.febslet.2010.08.049. Epub 2010 Sep 7.
RNA editing in plant mitochondria posttranscriptionally changes multiple cytidines to uridines. The RNA editing trans-factor MEF1 was identified via ecotype-specific editing polymorphisms in Arabidopsis thaliana. Complementation assays reveal that none of the three amino acid changes between Columbia (Col) and C24 individually alters RNA editing. Only one combination of these polymorphisms lowers editing at two of the three target sites, suggesting additive effects of the involved SNPs. Functional importance of the C-terminal DYW domain was analysed with DYW-truncated and extended constructs. These do not recover RNA editing in protoplasts and regain only low levels in stable transformants. In MEF1, the DYW domain is thus required for full competence in RNA editing and its C-terminus has to be accessible.
植物线粒体中的 RNA 编辑在后转录过程中将多个胞嘧啶转变为尿嘧啶。通过拟南芥生态型特异性编辑多态性,鉴定出 RNA 编辑转因子 MEF1。互补测定表明,哥伦比亚(Col)和 C24 之间的三个氨基酸变化中没有一个单独改变 RNA 编辑。只有这三种多态性的一种组合降低了三个靶位点中的两个的编辑水平,表明所涉及的 SNP 具有累加效应。用 DYW 截断和扩展构建体分析了 C 末端 DYW 结构域的功能重要性。这些在原生质体中不能恢复 RNA 编辑,在稳定转化体中仅恢复低水平。因此,在 MEF1 中,DYW 结构域对于 RNA 编辑的完全活性是必需的,并且其 C 末端必须是可及的。