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用寡核苷酸引物探测 Qβ 复制酶对 RNA 合成的合法起始。

Probing the legitimate initiation of RNA synthesis by Qβ replicase with oligonucleotide primers.

机构信息

Institute of Protein Research of the Russian Academy of Sciences, Pushchino, Russia.

出版信息

FEBS Lett. 2024 Mar;598(5):579-586. doi: 10.1002/1873-3468.14833. Epub 2024 Feb 26.

Abstract

Oligoribonucleotides complementary to the template 3' terminus were tested for their ability to initiate RNA synthesis on legitimate templates capable of exponential amplification by Qβ replicase. Oligonucleotides shorter than the distance to the nearest predicted template hairpin proved able to serve as primers, with the optimal length varying for different templates, suggesting that during initiation the template retains its native fold incorporating the 3' terminus. The priming activity of an oligonucleotide is greatly enhanced by its 5'-triphosphate group, the effect being strongly dependent on Mg ions. This indicates that, unlike other studied RNA polymerases, Qβ replicase binds the 5'-triphosphate of the initiating nucleotide GTP, and this binding is needed for the replication of legitimate templates.

摘要

寡核苷酸与模板 3'末端互补,被测试其在能够被 Qβ复制酶指数扩增的合法模板上起始 RNA 合成的能力。短于到最近预测的模板发夹的距离的寡核苷酸被证明能够作为引物,对于不同的模板,最佳长度不同,这表明在起始时,模板保持其天然折叠,包含 3'末端。寡核苷酸的引发活性被其 5'-三磷酸基团大大增强,该效应强烈依赖于 Mg 离子。这表明,与其他研究过的 RNA 聚合酶不同,Qβ复制酶结合起始核苷酸 GTP 的 5'-三磷酸基团,并且这种结合对于合法模板的复制是必需的。

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