Cheng Ming-Yu, Tao Wan-Bing, Yuan Bi-Feng, Feng Yu-Qi
Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), Sauvage Center for Molecular Sciences, Department of Chemistry, Wuhan University, Wuhan 430072, China.
Anal Methods. 2021 Jan 28;13(3):289-298. doi: 10.1039/d0ay01912g.
RNA molecules contain many chemical modifications that can regulate a variety of biological processes. Messenger RNA (mRNA) molecules are critical components in the central dogma of molecular biology. The discovery of reversible chemical modifications in eukaryotic mRNA brings forward a new research field in RNA modification-mediated regulation of gene expression. The modifications in mRNA generally exist in low abundance. The use of highly pure mRNA is critical for the confident identification of new modifications as well as for the accurate quantification of existing modifications in mRNA. In addition, isolation of highly pure mRNA is the first step in many biological research studies. Therefore, the methods for isolating highly pure mRNA are important for mRNA-based downstream studies. A variety of methods for isolating mRNA have been developed in the past few decades and new methods continuously emerge. This review focuses on the methodologies and protocols for isolating mRNA populations. In addition, we discuss the advantages and limitations of these methods. We hope this paper will provide a general view of mRNA isolation strategies and facilitate studies that involve mRNA modifications and functions.
RNA分子含有许多可调节多种生物过程的化学修饰。信使RNA(mRNA)分子是分子生物学中心法则的关键组成部分。真核生物mRNA中可逆化学修饰的发现开创了RNA修饰介导的基因表达调控这一新的研究领域。mRNA中的修饰通常以低丰度存在。使用高度纯化的mRNA对于可靠鉴定新修饰以及准确量化mRNA中现有修饰至关重要。此外,分离高度纯化的mRNA是许多生物学研究的第一步。因此,分离高度纯化mRNA的方法对于基于mRNA的下游研究很重要。在过去几十年中已经开发出多种分离mRNA的方法,并且新方法不断涌现。本综述重点关注分离mRNA群体的方法和方案。此外,我们讨论了这些方法的优缺点。我们希望本文能提供mRNA分离策略的总体概况,并促进涉及mRNA修饰和功能的研究。