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gRNA/pre-mRNA annealing and RNA chaperone activities of RBP16.

机译:RBP16的gRNA / pre-mRNA退火和RNA伴侣活性。

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Editing in trypanosomes involves the addition or deletion of uridines at specific sites to produce translatable mitochondrial mRNAs. RBP16 is an accessory factor from Trypanosoma brucei that affects mitochondrial RNA editing in vivo and also stimulates editing in vitro. We report here experiments aimed at elucidating the biochemical activities of RBP16 involved in modulating RNA editing. In vitro RNA annealing assays demonstrate that RBP16 significantly stimulates the annealing of gRNAs to cognate pre-mRNAs. In addition, RBP16 also facilitates hybridization of partially complementary RNAs unrelated to the editing process. The RNA annealing activity of RBP16 is independent of its high-affinity binding to gRNA oligo(U) tails, consistent with the previously reported in vitro editing stimulatory properties of the protein. In vivo studies expressing recombinant RBP16 in mutant Escherichia coli strains demonstrate that RBP16 is an RNA chaperone and that in addition to RNA annealing activity, it contains RNA unwinding activity. Our data suggest that the mechanism by which RBP16 facilitates RNA editing involves its capacity to modulate RNA secondary structure and promote gRNA/pre-mRNA annealing.
机译:锥虫体中的编辑涉及在特定位点添加或删除尿苷,以产生可翻译的线粒体mRNA。 RBP16是布鲁氏锥虫的辅助因子,可影响体内线粒体RNA编辑,并在体外刺激编辑。我们在这里报告旨在阐明参与调节RNA编辑的RBP16的生化活性的实验。体外RNA退火测定表明RBP16显着刺激了gRNA的退火,使其与前mRNA同源。另外,RBP16还促进与编辑过程无关的部分互补RNA的杂交。 RBP16的RNA退火活性与其与gRNA oligo(U)尾巴的高亲和力结合无关,这与先前报道的该蛋白的体外编辑刺激特性一致。在突变大肠杆菌菌株中表达重组RBP16的体内研究表明,RBP16是一种RNA分子伴侣,除了具有RNA退火活性外,它还具有RNA解链活性。我们的数据表明,RBP16促进RNA编辑的机制涉及其调节RNA二级结构并促进gRNA / pre-mRNA退火的能力。

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