Helwak Aleksandra, Tollervey David
Wellcome Trust Centre for Cell Biology, The University of Edinburgh, King's Buildings, Edinburgh, EH9 3BF, UK.
Methods Mol Biol. 2016;1358:229-51. doi: 10.1007/978-1-4939-3067-8_14.
We present a detailed protocol for the experimental identification of miRNA-target RNA interaction sites using cross-linking, ligation, and sequencing of hybrids (CLASH). The basis of the technique is the purification of UV-stabilized Argonaute (AGO)-RNA complexes assembled in living cells, with subsequent ligation of AGO-associated RNA-RNA duplexes to form chimeric RNAs. Following cDNA synthesis, DNA library preparation and high-throughput sequencing, interacting RNA molecules are unambiguously identified as chimeric reads in bioinformatic analysis of sequencing data. CLASH potentially recovers any RNA duplex that is bound by RNA-binding protein, so modified approaches would be suitable for the identification of many other inter- and intramolecular RNA-RNA interactions. Since CLASH analysis is independent of bioinformatic predictions it allows the identification and analysis of RNA targeting rules in an unbiased way.
我们展示了一种详细的实验方案,用于通过杂交体的交联、连接和测序(CLASH)对miRNA-靶RNA相互作用位点进行实验鉴定。该技术的基础是纯化在活细胞中组装的紫外线稳定的AGO-RNA复合物,随后连接与AGO相关的RNA-RNA双链体以形成嵌合RNA。在进行cDNA合成、DNA文库制备和高通量测序后,在测序数据的生物信息学分析中,相互作用的RNA分子被明确鉴定为嵌合读段。CLASH有可能回收任何被RNA结合蛋白结合的RNA双链体,因此经过改进的方法将适用于鉴定许多其他分子间和分子内的RNA-RNA相互作用。由于CLASH分析独立于生物信息学预测,它能够以无偏差的方式鉴定和分析RNA靶向规则。