{"title":"Transcriptome-Wide Mapping of m6A and m6Am at Single-Nucleotide Resolution Using miCLIP","authors":"Ben R. Hawley, Samie R. Jaffrey","doi":"10.1002/cpmb.88","DOIUrl":null,"url":null,"abstract":"<p>The most prevalent modified base in mRNA, <i>N</i><sup>6</sup>-methyladenosine (m<sup>6</sup>A), is found in several thousand transcripts, typically near the stop codon, although it can occur anywhere in the mRNA. In addition, the highly similar nucleotide <i>N</i><sup>6</sup>,2′-<i>O</i>-dimethyladenosine (m<sup>6</sup>Am), which is difficult to distinguish from m<sup>6</sup>A, occurs as the first transcribed nucleotide of certain transcripts. Both the m<sup>6</sup>A and m<sup>6</sup>Am modifications have been implicated in numerous biological processes, and their precise mapping is crucial to understanding their functions. To address this need, we developed miCLIP, a method that maps both m<sup>6</sup>A and m<sup>6</sup>Am at individual nucleotide resolution. Here we describe the miCLIP protocol, with slight improvements to the initially published protocol for both the experimental methodology and bioinformatics analysis. © 2019 by John Wiley & Sons, Inc.</p>","PeriodicalId":10734,"journal":{"name":"Current Protocols in Molecular Biology","volume":"126 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpmb.88","citationCount":"21","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Molecular Biology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpmb.88","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 21
Abstract
The most prevalent modified base in mRNA, N6-methyladenosine (m6A), is found in several thousand transcripts, typically near the stop codon, although it can occur anywhere in the mRNA. In addition, the highly similar nucleotide N6,2′-O-dimethyladenosine (m6Am), which is difficult to distinguish from m6A, occurs as the first transcribed nucleotide of certain transcripts. Both the m6A and m6Am modifications have been implicated in numerous biological processes, and their precise mapping is crucial to understanding their functions. To address this need, we developed miCLIP, a method that maps both m6A and m6Am at individual nucleotide resolution. Here we describe the miCLIP protocol, with slight improvements to the initially published protocol for both the experimental methodology and bioinformatics analysis. © 2019 by John Wiley & Sons, Inc.
m6A和m6Am在单核苷酸分辨率下的转录组定位
mRNA中最常见的修饰碱基n6 -甲基腺苷(m6A)存在于数千个转录本中,通常位于停止密码子附近,尽管它可以出现在mRNA的任何位置。此外,高度相似的核苷酸n6,2 ' - o -二甲基腺苷(m6Am)作为某些转录本的第一个转录核苷酸出现,难以与m6A区分。m6A和m6Am的修饰都与许多生物过程有关,它们的精确定位对于理解它们的功能至关重要。为了满足这一需求,我们开发了miCLIP,一种以单个核苷酸分辨率绘制m6A和m6Am的方法。在这里,我们描述了miCLIP方案,在实验方法和生物信息学分析方面对最初发表的方案进行了轻微改进。©2019 by John Wiley &儿子,Inc。
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