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转录组测序技术:解码 RNA 修饰。

Epitranscriptome sequencing technologies: decoding RNA modifications.

机构信息

State Key Laboratory of Protein and Plant Gene Research, School of Life Sciences, Peking University, Beijing, China.

Peking-Tsinghua Center for Life Sciences, Peking University, Beijing, China.

出版信息

Nat Methods. 2016 Dec 29;14(1):23-31. doi: 10.1038/nmeth.4110.

Abstract

In recent years, major breakthroughs in RNA-modification-mediated regulation of gene expression have been made, leading to the emerging field of epitranscriptomics.Our understanding of the distribution, regulation and function of these dynamic RNA modifications is based on sequencing technologies. In this Review, we focus on the major mRNA modifications in the transcriptome of eukaryotic cells: N6-methyladenosine, N6, 2'-O-dimethyladenosine, 5-methylcytidine, 5-hydroxylmethylcytidine, inosine, pseudouridine and N-methyladenosine. We discuss the sequencing technologies used to profile these epitranscriptomic marks, including scale, resolution, quantitative feature, pre-enrichment capability and the corresponding bioinformatics tools. We also discuss the challenges of epitranscriptome profiling and highlight the prospect of future detection tools. We aim to guide the choice of different detection methods and inspire new ideas in RNA biology.

摘要

近年来,RNA 修饰介导的基因表达调控取得了重大突破,催生了新兴的表观转录组学领域。我们对这些动态 RNA 修饰的分布、调控和功能的理解依赖于测序技术。在这篇综述中,我们重点介绍真核细胞转录组中主要的 mRNA 修饰:N6-甲基腺苷、N6,2'-O-二甲基腺苷、5-甲基胞嘧啶、5-羟甲基胞嘧啶、次黄嘌呤、假尿嘧啶和 N6-甲基腺苷。我们讨论了用于描绘这些表观转录组标记的测序技术,包括其规模、分辨率、定量特征、预富集能力以及相应的生物信息学工具。我们还讨论了表观转录组分析的挑战,并强调了未来检测工具的前景。我们旨在指导不同检测方法的选择,并为 RNA 生物学激发新的思路。

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