RNA序列
免疫沉淀
非翻译区
计算生物学
核糖核酸
基因表达
生物
基因
遗传学
转录组
作者
Meiling Zhang,Hanxiao Sun,Kai Li,Ye Xiao,Chengqi Yi
出处
期刊:Methods
[Elsevier]
日期:2021-10-07
卷期号:203: 242-248
被引量:9
标识
DOI:10.1016/j.ymeth.2021.10.001
摘要
Reversible and dynamic RNA modifications play important roles in fine-tuning gene expression. N6, 2'-O-dimethyladenosine (m6Am), a terminal modification at mRNA cap, mediates various biological effects. However, limitations of the current m6Am detection methods lead to a lack of potential applications. Here, we describe a specific and sensitive method, termed m6Am-seq, that can detect m6Am at single-base resolution. m6Am-seq is based on optimized in-vitro demethylation assay and RNA immunoprecipitation, which can distinguish m6Am from 5'-UTR m6A. We provide a step by step protocol to perform m6Am-seq, including experimental procedures and sequencing data analysis. Collectively, we describe m6Am-seq, a robust tool to reveal both m6Am and 5'-UTR m6A methylome, enabling further functional and mechanistic study of m6Am modification.
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