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The dynamic N(1)-methyladenosine methylome in eukaryotic messenger RNA.真核生物信使核糖核酸中的动态N(1)-甲基腺苷甲基化组
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The epitranscriptome in modulating spatiotemporal RNA translation in neuronal post-synaptic function.表观转录组在调节神经元突触后功能中的时空RNA翻译过程中的作用。
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Bidirectional Direct Sequencing of Noncanonical RNA by Two-Dimensional Analysis of Mass Chromatograms.通过质量色谱图的二维分析对非规范RNA进行双向直接测序
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走向全球:RNA修饰图谱绘制的新时代。

Going global: the new era of mapping modifications in RNA.

作者信息

Limbach Patrick A, Paulines Mellie June

机构信息

Department of Chemistry, University of Cincinnati, Cincinnati, OH, USA.

出版信息

Wiley Interdiscip Rev RNA. 2017 Jan;8(1). doi: 10.1002/wrna.1367. Epub 2016 Jun 1.

DOI:10.1002/wrna.1367
PMID:27251302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5133204/
Abstract

The post-transcriptional modification of RNA by the addition of one or more chemical groups has been known for over 50 years. These chemical modifications, once thought to be static, are now being discovered to play key regulatory roles in gene expression. The advent of massive parallel sequencing of RNA (RNA-seq) now allows us to probe the complexity of cellular RNA and how chemically altering RNA structure expands the RNA vocabulary. Here we present an overview of the various strategies and technologies that are available to profile RNA chemical modifications at the cellular level. These strategies can be characterized as targeted and untargeted approaches: targeted strategies are developed for one single chemical modification while untargeted strategies are more broadly applicable to a range of such chemical changes. Key for all of these approaches is the ability to locate modifications within the RNA sequence. While most of these methods are built upon an RNA-Seq pipeline, alternative approaches based on mass spectrometry or conventional DNA sequencing retain value in the overall analysis process. We also look forward toward future opportunities and technologies that may expand the types of modifications that can be globally profiled. Given the ever increasing recognition that these RNA chemical modifications play important biological roles, a variety of methods, preferably orthogonal approaches, will be required to globally identify, validate and quantify RNA chemical modifications found in the transcriptome. WIREs RNA 2017, 8:e1367. doi: 10.1002/wrna.1367 For further resources related to this article, please visit the WIREs website.

摘要

通过添加一个或多个化学基团对RNA进行转录后修饰已经为人所知五十多年了。这些化学修饰曾经被认为是静态的,现在人们发现它们在基因表达中发挥着关键的调节作用。RNA大规模平行测序(RNA-seq)的出现,使我们能够探究细胞RNA的复杂性,以及化学改变RNA结构如何扩展RNA的功能。在这里,我们概述了在细胞水平上分析RNA化学修饰的各种策略和技术。这些策略可分为靶向和非靶向方法:靶向策略是针对单一化学修饰开发的,而非靶向策略更广泛地适用于一系列此类化学变化。所有这些方法的关键在于能够在RNA序列中定位修饰。虽然这些方法大多基于RNA-Seq流程,但基于质谱或传统DNA测序的替代方法在整个分析过程中仍具有价值。我们还展望了未来可能扩展可进行全局分析的修饰类型的机会和技术。鉴于人们越来越认识到这些RNA化学修饰发挥着重要的生物学作用,需要多种方法,最好是正交方法,来全局识别、验证和量化转录组中发现的RNA化学修饰。WIREs RNA 2017, 8:e1367. doi: 10.1002/wrna.1367 有关本文的更多资源,请访问WIREs网站。