Department of Chemistry, Princeton University, Princeton, New Jersey 08544, United States.
ACS Chem Biol. 2022 Mar 18;17(3):503-508. doi: 10.1021/acschembio.1c00707. Epub 2022 Feb 25.
Epitranscriptomic RNA modifications can regulate biological processes, but there remains a major gap in our ability to identify and measure individual modifications at nucleotide resolution. Here we present Mal-Seq, a chemical method for sequencing 5-formylcytosine (fC) modifications on RNA based on the selective and efficient malononitrile-mediated labeling of fC residues to generate adducts that are read as C-to-T mutations upon reverse transcription and polymerase chain reaction amplification. We apply Mal-Seq to characterize the prevalence of fC at the wobble position of mt-tRNA(Met) in different organisms and tissue types and find that high-level fC modification is present in mammals but lacking in lower eukaryotes. Our work sheds light on mitochondrial tRNA modifications throughout eukaryotic evolution and provides a general platform for characterizing the fC epitranscriptome.
表观转录组 RNA 修饰可以调节生物过程,但我们在识别和测量核苷酸分辨率下的单个修饰方面的能力仍存在很大差距。在这里,我们提出了 Mal-Seq,这是一种基于 5-甲酰胞嘧啶(fC)残基的选择性和高效的丙二腈介导标记来生成加合物的方法,该方法可将 fC 残基标记为 C 到 T 的突变,从而在反转录和聚合酶链反应扩增后进行读取。我们应用 Mal-Seq 来描述不同生物和组织类型中 mt-tRNA(Met)的摆动位置上 fC 的普遍性,并发现高水平的 fC 修饰存在于哺乳动物中,但在低等真核生物中缺失。我们的工作揭示了真核生物进化过程中线粒体 tRNA 修饰的情况,并为描述 fC 表观转录组提供了一个通用平台。