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Identification of a selective DNA ligase for accurate recognition and ultrasensitive quantification of N6-methyladenosine in RNA at one-nucleotide resolution

机译:鉴定一种选择性DNA连接酶以一核苷酸的分辨率精确识别RNA中的N6-甲基腺苷并进行超灵敏定量

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摘要

N 6-Methyladenosine (m6A) is the most frequent post-transcriptional modification in RNA, and it plays a critical role in biological processes. The functions of m6A remain largely unexplored due to a lack of highly sensitive methods to quantitatively determine the m6A modification fraction at a precise location. Here, we first reveal that T3 DNA ligase has significant selectivity towards the m6A modification. On the basis of the new finding, we establish an ultrasensitive quantitation assay for accurately determining m6A at one-nucleotide resolution in RNA. With the proposed assay, as low as 4 fM RNA containing m6A can be determined and the selectivity is up to 54.1-fold to discriminate m6A against unmodified adenosine (A). The sensitivity has been improved about 106-fold so the proposed method can be successfully employed to accurately determine m6A in real biological samples, even in low abundance RNA.
机译:N 6 -甲基腺苷(m 6 A)是RNA中最常见的转录后修饰,在生物学过程中起着至关重要的作用。由于缺乏精确地定量确定m 6 A修饰分数的高度灵敏的方法,因此m 6 A的功能仍未开发。在这里,我们首先揭示T3 DNA连接酶对m 6 A修饰具有明显的选择性。在这一新发现的基础上,我们建立了一种超灵敏定量测定法,用于以RNA中的一个核苷酸分辨率准确测定m 6 A。通过提出的测定方法,可以确定低至4 mM的含有m 6 A的RNA,并且选择性高达54.1倍,可以区分m 6 A与未修饰的腺苷(一个)。灵敏度提高了约10 6 倍,因此该方法可以成功地准确测定真实生物样品中的m 6 A,即使在低丰度RNA中也是如此。

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