Cheng Y W, Visomirski-Robic L M, Gott J M
Center for RNA Molecular Biology, Department of Molecular Biology and Microbiology, Case Western Reserve University School of Medicine, 10900 Euclid Avenue, Cleveland, OH 44106, USA.
EMBO J. 2001 Mar 15;20(6):1405-14. doi: 10.1093/emboj/20.6.1405.
RNAs in Physarum: mitochondria contain extra nucleotides that are not encoded by the mitochondrial genome, at least in the traditional sense. While it is known that insertion of non-encoded nucleotides is linked to RNA synthesis, the exact nature of this relationship remains unclear. Here we demonstrate that the efficiency of editing is sensitive not only to the concentration of the nucleotide that is inserted, but also to the concentration of the nucleotide templated just downstream of an editing site. These data strongly support a co-transcriptional mechanism of Physarum: RNA editing in which non-encoded nucleotides are added to the 3' end of nascent RNAs. These results also suggest that transcription elongation and nucleotide insertion are competing processes and that recognition of editing sites most likely involves transient pausing by the Physarum: mitochondrial RNA polymerase. In addition, the pattern of nucleotide concentration effects, the context of editing sites and the accuracy of the mitochondrial RNA polymerase argue that the mechanism of Physarum: editing is distinct from that of other co-transcriptional editing systems.
黏菌中的RNA:线粒体含有额外的核苷酸,至少在传统意义上,这些核苷酸不是由线粒体基因组编码的。虽然已知非编码核苷酸的插入与RNA合成有关,但这种关系的确切性质仍不清楚。在这里,我们证明编辑效率不仅对插入的核苷酸浓度敏感,而且对编辑位点下游紧邻的模板化核苷酸浓度也敏感。这些数据有力地支持了黏菌的共转录机制:RNA编辑,即在新生RNA的3'末端添加非编码核苷酸。这些结果还表明转录延伸和核苷酸插入是相互竞争的过程,并且编辑位点的识别很可能涉及黏菌线粒体RNA聚合酶的短暂暂停。此外,核苷酸浓度效应模式、编辑位点的背景以及线粒体RNA聚合酶的准确性表明,黏菌的编辑机制与其他共转录编辑系统不同。