Chan Dalen, Feng Chao, Spitale Robert C
Department of Pharmaceutical Sciences, University of California, Irvine, Irvine, CA 92697, United States.
Department of Pharmaceutical Sciences, University of California, Irvine, Irvine, CA 92697, United States; Department of Chemistry, University of California, Irvine, Irvine, CA 92697, United States.
Methods. 2017 May 1;120:85-90. doi: 10.1016/j.ymeth.2017.02.010. Epub 2017 Mar 20.
RNA molecules can be found at the heart of nearly every aspect of gene regulation: from gene expression to protein translation. The ability of RNA molecules to fold into intricate structures guides their function. Chemical methods to measure RNA structure have been part of the RNA biologists toolkit for several decades. These methods, although often cumbersome and difficult to perform on large RNAs, are notable for their accuracy and precision of structural measurements. Recent extension of these methods to transcriptome-wide analyses has opened the door to interrogating the structure of complete RNA molecules inside cells. Within this manuscript we describe the biochemical basis for the methodology behind a novel technology, icSHAPE, which measures RNA flexibility and single-strandedness in RNA. Novel methods such as icSHAPE have greatly expanded our understanding of RNA function and have paved the way to expansive analyses of large groups of RNA structures as they function inside the native environment of the cell.
RNA分子几乎存在于基因调控的各个核心环节:从基因表达至蛋白质翻译。RNA分子折叠成复杂结构的能力决定了它们的功能。几十年来,用于测量RNA结构的化学方法一直是RNA生物学家工具库的一部分。这些方法虽然通常操作繁琐,且难以应用于大型RNA,但在结构测量的准确性和精确性方面表现出色。最近,这些方法扩展到全转录组分析,为研究细胞内完整RNA分子的结构打开了大门。在本论文中,我们描述了一种新技术icSHAPE背后方法的生化基础,该技术可测量RNA的柔韧性和单链性。诸如icSHAPE之类的新方法极大地扩展了我们对RNA功能的理解,并为在细胞天然环境中发挥作用的大量RNA结构的广泛分析铺平了道路。