a Department of Molecular Genetics , Weizmann Institute of Science , Rehovot , Israel.
b Laboratoire IMoPA, UMR7365 CNRS-UL, Biopole Lorraine University , Vandoeuvre-les-Nancy , France.
RNA Biol. 2017 Sep 2;14(9):1124-1137. doi: 10.1080/15476286.2016.1251543. Epub 2016 Oct 28.
Our ability to map and quantify RNA modifications at a genome-wide scale have revolutionized our understanding of the pervasiveness and dynamic regulation of diverse RNA modifications. Recent efforts in the field have demonstrated the presence of modified residues in almost any type of cellular RNA. Next-generation sequencing (NGS) technologies are the primary choice for transcriptome-wide RNA modification mapping. Here we provide an overview of approaches for RNA modification detection based on their RT-signature, specific chemicals, antibody-dependent (Ab) enrichment, or combinations thereof. We further discuss sources of artifacts in genome-wide modification maps, and experimental and computational considerations to overcome them. The future in this field is tightly linked to the development of new specific chemical reagents, highly specific Ab against RNA modifications and use of single-molecule RNA sequencing techniques.
我们在全基因组范围内绘制和定量 RNA 修饰的能力极大地改变了我们对各种 RNA 修饰的普遍性和动态调控的理解。该领域的最新研究表明,几乎所有类型的细胞 RNA 中都存在修饰残基。下一代测序(NGS)技术是全转录组 RNA 修饰图谱绘制的首选方法。在这里,我们根据 RT 特征、特定化学物质、抗体依赖(Ab)富集或它们的组合,提供了一种用于 RNA 修饰检测的方法概述。我们还进一步讨论了全基因组修饰图谱中产生的假象的来源,以及克服这些假象的实验和计算考虑因素。该领域的未来与新型特异性化学试剂、针对 RNA 修饰的高度特异性抗体以及使用单分子 RNA 测序技术的发展紧密相关。