Groupe ARN (RNA Group), Laboratoire de Génomique Fonctionnelle (Laboratory for Functional Genomics), Département de Microbiologie et d'Infectiologie, Faculté de Médecine et des Sciences de la Santé, Université de Sherbrooke, Sherbrooke, Québec, Canada.
PLoS One. 2007 May 30;2(5):e472. doi: 10.1371/journal.pone.0000472.
In eukaryotes, short RNAs guide a variety of enzymatic activities that range from RNA editing to translation repression. It is hypothesized that pre-existing proteins evolved to bind and use guide RNA during evolution. However, the capacity of modern proteins to adopt new RNA guides has never been demonstrated. Here we show that Rnt1p, the yeast orthologue of the bacterial dsRNA-specific RNase III, can bind short RNA transcripts and use them as guides for sequence-specific cleavage. Target cleavage occurred at a constant distance from the Rnt1p binding site, leaving the guide RNA intact for subsequent cleavage. Our results indicate that RNase III may trigger sequence-specific RNA degradation independent of the RNAi machinery, and they open the road for a new generation of precise RNA silencing tools that do not trigger a dsRNA-mediated immune response.
在真核生物中,短 RNA 指导各种酶活性,范围从 RNA 编辑到翻译抑制。据推测,在进化过程中,现有的蛋白质进化为结合并使用指导 RNA。然而,现代蛋白质是否能够采用新的 RNA 向导还从未得到证实。在这里,我们展示了酵母中细菌 dsRNA 特异性 RNase III 的同源物 Rnt1p 可以结合短 RNA 转录本,并将其用作序列特异性切割的向导。靶切割发生在距 Rnt1p 结合位点恒定距离处,从而使向导 RNA 保持完整,以备后续切割。我们的结果表明,RNase III 可能触发独立于 RNAi 机制的序列特异性 RNA 降解,并且为新一代不触发 dsRNA 介导的免疫反应的精确 RNA 沉默工具开辟了道路。