Department of Molecular Biology, Howard Hughes Medical Institute, Massachusetts General Hospital, Boston, United States.
Center for Computational and IntegrativeBiology, Massachusetts General Hospital, Boston, United States.
Elife. 2019 Nov 8;8:e51888. doi: 10.7554/eLife.51888.
Non-enzymatic RNA self-replication is integral to the emergence of the 'RNA World'. Despite considerable progress in non-enzymatic template copying, demonstrating a full replication cycle remains challenging due to the difficulty of separating the strands of the product duplex. Here, we report a prebiotically plausible approach to strand displacement synthesis in which short 'invader' oligonucleotides unwind an RNA duplex through a toehold/branch migration mechanism, allowing non-enzymatic primer extension on a template that was previously occupied by its complementary strand. Kinetic studies of single-step reactions suggest that following invader binding, branch migration results in a 2:3 partition of the template between open and closed states. Finally, we demonstrate continued primer extension with strand displacement by employing activated 3'-aminonucleotides, a more reactive proxy for ribonucleotides. Our study suggests that complete cycles of non-enzymatic replication of the primordial genetic material may have been facilitated by short RNA oligonucleotides.
非酶 RNA 自我复制是“RNA 世界”出现的关键。尽管在非酶模板复制方面取得了相当大的进展,但由于难以分离产物双链的链,证明完整的复制循环仍然具有挑战性。在这里,我们报告了一种前生物上合理的链置换合成方法,其中短的“入侵”寡核苷酸通过钉位/分支迁移机制解开 RNA 双链,从而允许在先前被互补链占据的模板上进行非酶引物延伸。单步反应的动力学研究表明,在入侵结合后,分支迁移导致模板在打开和关闭状态之间以 2:3 的比例分配。最后,我们通过使用活化的 3'-氨基核苷酸(更具反应性的核糖核苷酸代理)来证明通过链置换的持续引物延伸。我们的研究表明,短 RNA 寡核苷酸可能促进了原始遗传物质的非酶复制的完整循环。