Verbitskiy Daniil, van der Merwe Johannes A, Zehrmann Anja, Brennicke Axel, Takenaka Mizuki
Institut für Molekulare Botanik, Universität Ulm, 89069 Ulm, Germany.
J Biol Chem. 2008 Sep 5;283(36):24374-81. doi: 10.1074/jbc.M803292200. Epub 2008 Jul 1.
Analysis of RNA editing in plant mitochondria has at least in vitro been hampered by very low activity. Consequently, none of the trans-acting factors involved has yet been identified. We here report that in vitro RNA editing increases dramatically when additional cognate recognition motifs are introduced into the template RNA molecule. Substrate RNAs with tandemly repeated recognition elements enhance in vitro RNA editing from 2-3% to 50-80%. The stimulation is not influenced by the editing status of a respective RNA editing site, suggesting that specific recognition of a site can be independent of the edited nucleotide itself. In vivo, attachment of the editing complex may thus be analogously initiated at sequence similarities in the vicinity of bona fide editing sites. This cis-acting enhancement decreases with increasing distance between the duplicated specificity signals; a cooperative effect is detectable up to approximately 200 nucleotides. Such repeated template constructs promise to be powerful tools for the RNA affinity identification of the as yet unknown trans-factors of plant mitochondrial RNA editing.
植物线粒体中RNA编辑的分析至少在体外受到极低活性的阻碍。因此,尚未鉴定出任何相关的反式作用因子。我们在此报告,当将额外的同源识别基序引入模板RNA分子时,体外RNA编辑会显著增加。具有串联重复识别元件的底物RNA可将体外RNA编辑从2%-3%提高到50%-80%。这种刺激不受相应RNA编辑位点编辑状态的影响,这表明对位点的特异性识别可能独立于被编辑的核苷酸本身。在体内,编辑复合体的附着可能因此类似地在真正编辑位点附近的序列相似性处启动。这种顺式作用增强随着重复特异性信号之间距离的增加而降低;在大约200个核苷酸范围内可检测到协同效应。这种重复模板构建体有望成为用于RNA亲和鉴定植物线粒体RNA编辑中尚未知的反式因子的强大工具。