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mRNA修饰的测序方法与功能解码

Sequencing methods and functional decoding of mRNA modifications.

作者信息

Li Kai, Peng Jinying, Yi Chengqi

机构信息

State Key Laboratory of Protein and Plant Gene Research, School of Life Sciences, Peking University, Beijing 100871, China.

Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, 100871, China.

出版信息

Fundam Res. 2023 Jun 1;3(5):738-748. doi: 10.1016/j.fmre.2023.05.010. eCollection 2023 Sep.

Abstract

More than 160 types of post-transcriptional RNA modifications have been reported; there is substantial variation in modification type, abundance, site, and function across species, tissues, and RNA type. The recent development of high-throughput detection technology has enabled identification of diverse dynamic and reversible RNA modifications, including N6,2'-O-dimethyladenosine (m6Am), N1-methyladenosine (m1A), 5-methylcytosine (m5C), N6-methyladenosine (m6A), pseudouridine (Ψ), and inosine (I). In this review, we focus on eukaryotic mRNA modifications. We summarize their biogenesis, regulatory mechanisms, and biological functions, as well as high-throughput methods for detection of mRNA modifications. We also discuss challenges that must be addressed in mRNA modification research.

摘要

据报道,转录后RNA修饰类型超过160种;修饰类型、丰度、位点及功能在不同物种、组织和RNA类型间存在显著差异。高通量检测技术的最新进展使得鉴定多种动态可逆的RNA修饰成为可能,包括N6,2'-O-二甲基腺苷(m6Am)、N1-甲基腺苷(m1A)、5-甲基胞嘧啶(m5C)、N6-甲基腺苷(m6A)、假尿苷(Ψ)和肌苷(I)。在本综述中,我们聚焦于真核生物mRNA修饰。我们总结了它们的生物合成、调控机制及生物学功能,以及检测mRNA修饰的高通量方法。我们还讨论了mRNA修饰研究中必须解决的挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/216f/11197720/3e4f2864ba91/gr1.jpg

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