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用于阐明活性生成单元的I类连接酶核酶的分子剖析

Molecular Anatomy of the Class I Ligase Ribozyme for Elucidation of the Activity-Generating Unit.

作者信息

Kasuga Miho, Mutsuro-Aoki Hiromi, Ando Tadashi, Tamura Koji

机构信息

Department of Biological Science and Technology, Tokyo University of Science, 6-3-1 Niijuku, Katsushika-ku, Tokyo 125-8585, Japan.

Department of Applied Electronics, Tokyo University of Science, 6-3-1 Niijuku, Katsushika-ku, Tokyo 125-8585, Japan.

出版信息

Biology (Basel). 2023 Jul 17;12(7):1012. doi: 10.3390/biology12071012.

Abstract

The class I ligase ribozyme consists of 121 nucleotides and shows a high catalytic rate comparable to that found in natural proteinaceous polymerases. In this study, we aimed to identify the smaller active unit of the class I ligase ribozyme comprising ~50 nucleotides, comparable to the estimated length of prebiotically synthesized RNA. Based on the three-dimensional structure of the class I ligase ribozyme, mutants were prepared and their ligation activities were analyzed. Sufficient ligation activity was maintained even when shortening to 94 nucleotides. However, because it would be difficult to approach the target of ~50 nucleotides by removing only the partial structure, the class I ligase ribozyme was then split into two molecules. The ligation activity was maintained even when splitting into two molecules of 55 and 39 nucleotides. Using a system with similar split ribozymes, we analyzed the ligation activity of mutants C30, C47, and A71, which have been previously identified as the positions that contribute to catalytic activity, and discussed the structural basis of the activity of these bases. Our findings suggest the rationale for the class I ligase ribozyme's assembling from multiple fragments that would be achievable with prebiotic synthesis.

摘要

I类连接酶核酶由121个核苷酸组成,其催化速率与天然蛋白质聚合酶相当。在本研究中,我们旨在鉴定I类连接酶核酶的较小活性单位,其包含约50个核苷酸,这与益生元合成RNA的估计长度相当。基于I类连接酶核酶的三维结构,制备了突变体并分析了它们的连接活性。即使缩短至94个核苷酸,仍能保持足够的连接活性。然而,由于仅通过去除部分结构难以达到约50个核苷酸的目标,因此将I类连接酶核酶分成两个分子。即使分成55和39个核苷酸的两个分子,连接活性仍得以保持。使用具有类似分裂核酶的系统,我们分析了先前已确定为对催化活性有贡献的位置的突变体C30、C47和A71的连接活性,并讨论了这些碱基活性的结构基础。我们的研究结果表明了I类连接酶核酶由益生元合成可能实现的多个片段组装而成的原理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df55/10376402/1156bd925ddb/biology-12-01012-g001.jpg

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