Suppr超能文献

使用CLASH鉴定微小RNA-靶RNA相互作用

Identification of miRNA-Target RNA Interactions Using CLASH.

作者信息

Helwak Aleksandra, Tollervey David

机构信息

Wellcome Trust Centre for Cell Biology, The University of Edinburgh, King's Buildings, Edinburgh, EH9 3BF, UK.

出版信息

Methods Mol Biol. 2016;1358:229-51. doi: 10.1007/978-1-4939-3067-8_14.

Abstract

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.

摘要

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。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验