Peking University Chengdu Academy for Advanced Interdisciplinary Biotechnologies, Chengdu, China; Peking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.
Peking University Chengdu Academy for Advanced Interdisciplinary Biotechnologies, Chengdu, China.
Curr Opin Genet Dev. 2024 Aug;87:102212. doi: 10.1016/j.gde.2024.102212. Epub 2024 May 31.
The epitranscriptome encompasses a diverse array of dynamic and reversible RNA modifications, affecting both coding and noncoding RNAs. Over 170 types of RNA chemical modifications have been identified, underscoring the need for innovative detection methods to deepen our understanding of RNA modification roles and mechanisms. In particular, the base resolution and quantitative information on RNA modifications are critical for understanding the regulation and functions of RNA modifications. Based on detection throughput and principles, existing quantitative RNA modification detection methods can be categorized into two groups, including next-generation sequencing and nanopore direct RNA sequencing. In this review, we focus on methodologies for elucidating the base resolution and stoichiometric information of RNA modifications. In addition, we further discuss the challenges and the potential prospects of the quantitative RNA modification detection methods.
表观转录组包含广泛多样的动态和可逆的 RNA 修饰,影响编码和非编码 RNA。已经鉴定出超过 170 种 RNA 化学修饰类型,这凸显了需要创新的检测方法来加深我们对 RNA 修饰作用和机制的理解。特别是,RNA 修饰的碱基分辨率和定量信息对于理解 RNA 修饰的调控和功能至关重要。基于检测通量和原理,现有的定量 RNA 修饰检测方法可以分为两类,包括下一代测序和纳米孔直接 RNA 测序。在这篇综述中,我们重点介绍了阐明 RNA 修饰的碱基分辨率和化学计量信息的方法。此外,我们还进一步讨论了定量 RNA 修饰检测方法的挑战和潜在前景。