State Key Laboratory of Coordination Chemistry, Department of Biomedical Engineering, College of Engineering and Applied Sciences, Jiangsu Key Laboratory of Artificial Functional Materials, Chemistry and Biomedicine Innovation Center (ChemBIC), Nanjing University, Nanjing, Jiangsu 210023, China.
Applied Adaptome Immunology Institute, Jiangsu Industrial Technology Research Institute, Nanjing, Jiangsu 210023, China.
J Am Chem Soc. 2021 Jun 2;143(21):8154-8163. doi: 10.1021/jacs.1c02895. Epub 2021 May 24.
Threose nucleic acid (TNA) has been considered a potential RNA progenitor in evolution due to its chemical simplicity and base pairing property. Catalytic TNA sequences with RNA ligase activities might have facilitated the transition to the RNA world. Here we report the isolation of RNA ligase TNA enzymes by selection. The identified TNA enzyme T8-6 catalyzes the formation of a 2'-5' phosphoester bond between a 2',3'-diol and a 5'-triphosphate group, with a of 1.1 × 10 min (40 mM Mg, pH 9.0). For efficient reaction, T8-6 requires UA|GA at the ligation junction and tolerates variations at other substrate positions. Functional RNAs such as hammerhead ribozyme can be prepared by T8-6-catalyzed ligation, with site-specific introduction of a 2'-5' linkage. Together, this work provides experimental support for TNA as a plausible pre-RNA genetic polymer and also offers an alternative molecular tool for biotechnology.
三碳核酸(TNA)由于其化学简单性和碱基配对性质,被认为是进化过程中潜在的 RNA 前体。具有 RNA 连接酶活性的催化 TNA 序列可能促进了向 RNA 世界的转变。在这里,我们通过选择报道了 RNA 连接酶 TNA 酶的分离。鉴定出的 TNA 酶 T8-6 催化 2',3'-二醇和 5'-三磷酸基团之间形成 2'-5'磷酸酯键,其 为 1.1×10 min(40 mM Mg,pH 9.0)。为了有效反应,T8-6 在连接接头处需要 UA|GA,并容忍其他底物位置的变化。T8-6 催化的连接可以制备功能性 RNA,如锤头核酶,并在特定位置引入 2'-5'键。总之,这项工作为 TNA 作为一种合理的前 RNA 遗传聚合物提供了实验支持,也为生物技术提供了一种替代的分子工具。