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Cross-linking, ligation, and sequencing of hybrids reveals RNA-RNA interactions in yeast

机译:杂种的交联,连接和测序揭示了酵母中的RNA-RNA相互作用

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摘要

Many protein-protein and protein-nucleic acid interactions have been experimentally characterized, whereas RNA-RNA interactions have generally only been predicted computationally. Here, we de scribe a high-throughput method to identify intramolecular and intermolecular RNA-RNA interactions, experimentally by cross linking, ligation, and sequencing of hybrids (CLASH). As validation, we identified 39 known target sites for box C/D modification-guide small nucleolar RNAs (snoRNAs) on the yeast pre-rRNA. Novel snoRNA-rRNA hybrids were recovered between snR4-5S and U14- 25S. These are supported by native electrophoresis and consistent with previously unexplained data. The U3 snoRNA was found to be associated with sequences close to the 3' side of the central pseu doknot in 18S rRNA, supporting a role in formation of this structure. Applying CLASH to the yeast U2 spliceosomal snRNA led to a revised predicted secondary structure, featuring alternative folding of the 3' domain and long-range contacts between the 3' and 5' domains. CLASH should allow transcriptome-wide analyses of RNA-RNA interactions in many organisms.
机译:已经通过实验表征了许多蛋白质-蛋白质和蛋白质-核酸相互作用,而RNA-RNA相互作用通常仅是通过计算预测的。在这里,我们描述了一种高通量方法,可通过交联,连接和杂交体测序(CLASH)实验性地鉴定分子内和分子间RNA-RNA相互作用。作为验证,我们为酵母前rRNA上的框C / D修饰指导小核仁RNA(snoRNA)确定了39个已知靶位。在snR4-5S和U14-25S之间回收了新的snoRNA-rRNA杂种。这些由天然电泳支持,并与以前无法解释的数据一致。 U3 snoRNA被发现与18S rRNA中靠近中央pseu齿的3'侧的序列相关,支持这种结构的形成。将CLASH应用于酵母U2剪接体snRNA导致修订的预测二级结构,其特征在于3'结构域的交替折叠以及3'和5'结构域之间的长距离接触。 CLASH应该允许在许多生物中进行转录组范围的RNA-RNA相互作用分析。

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