Zhang Stephanie J, Jia Xiwen, DasGupta Saurja, Szostak Jack W
Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts 02115, United States.
Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, United States.
bioRxiv. 2025 Jul 12:2025.07.11.664453. doi: 10.1101/2025.07.11.664453.
Nonenzymatic assembly of activated RNA building blocks, such as phosphorimidazolides, would have been essential for the emergence of ribozymes on the early Earth. We previously showed that ribonucleoside monophosphates can be activated to phosphorimidazolides via a prebiotically relevant phospho-Passerini reaction involving 2-aminoimidazole, 2-methylbutyraldehyde, and methyl isocyanide, and that these activated nucleotides enable template-directed nonenzymatic RNA polymerization in the same reaction mixture. Here, we demonstrate that the same chemistry activates oligoribonucleotides and drives both nonenzymatic and ribozyme-catalyzed RNA ligation within the same reaction environment. By demonstrating a continuous path from prebiotic activation chemistry to RNA template copying by both nonenzymatic and ribozyme-catalyzed ligation, our results provide a more integrated and realistic model for RNA assembly on the early Earth.
对于早期地球上核酶的出现而言,诸如磷酰咪唑化物等活化RNA构建模块的非酶促组装必不可少。我们之前表明,核糖核苷单磷酸可通过涉及2-氨基咪唑、2-甲基丁醛和甲基异氰化物的与生命起源相关的磷酰-帕瑟里尼反应被活化成磷酰咪唑化物,并且这些活化的核苷酸能够在同一反应混合物中实现模板导向的非酶促RNA聚合。在此,我们证明相同的化学反应能活化寡核糖核苷酸,并在同一反应环境中驱动非酶促和核酶催化的RNA连接。通过展示从生命起源前的活化化学到通过非酶促和核酶催化连接进行RNA模板复制的连续路径,我们的结果为早期地球上的RNA组装提供了一个更完整、更现实的模型。