Yang Weiwei, Dai Nan, Lin Yu-Cheng, Johnson William, Vaisvila Romualdas, Weigele Peter, Lee Yan-Jiun, Schildkraut Ira, Corrêa Ivan R, Ettwiller Laurence
New England Biolabs, Ipswich, United States.
Bio Protoc. 2022 Sep 5;12(17). doi: 10.21769/BioProtoc.4496.
Nucleic acids in living organisms are more complex than the simple combinations of the four canonical nucleotides. Recent advances in biomedical research have led to the discovery of numerous naturally occurring nucleotide modifications and enzymes responsible for the synthesis of such modifications. In turn, these enzymes can be leveraged towards toolkits for DNA and RNA manipulation for epigenetic sequencing or other biotechnological applications. Here, we present the protocol to obtain purified 5-hydroxymethylcytosine carbamoyltransferase enzymes and the associated assays to convert 5-hydroxymethylcytosine to 5-carbamoyloxymethylcytosine . We include detailed assays using DNA, RNA, and single nucleotide/deoxynucleotide as substrates. These assays can be combined with downstream applications for genetic/epigenetic regulatory mechanism studies and next-generation sequencing purposes.
活生物体中的核酸比四种标准核苷酸的简单组合更为复杂。生物医学研究的最新进展已导致发现了众多天然存在的核苷酸修饰以及负责此类修饰合成的酶。反过来,这些酶可用于构建用于DNA和RNA操作的工具包,以进行表观遗传测序或其他生物技术应用。在此,我们展示了获取纯化的5-羟甲基胞嘧啶氨甲酰基转移酶的方案以及将5-羟甲基胞嘧啶转化为5-氨甲酰氧基甲基胞嘧啶的相关测定方法。我们包括使用DNA、RNA和单核苷酸/脱氧核苷酸作为底物的详细测定方法。这些测定方法可与用于遗传/表观遗传调控机制研究和下一代测序目的的下游应用相结合。