Kurihara Eri, Uchida Sayuri, Umehara Takuya, Tamura Koji
Department of Biological Science and Technology, Tokyo University of Science, 6-3-1 Niijuku, Katsushika-ku, Tokyo 125-8585, Japan.
Biology (Basel). 2014 Jul 29;3(3):452-65. doi: 10.3390/biology3030452.
The R3C ligase ribozyme is an artificial ligase ribozyme produced by modification of the ribozyme that lacks cytidine. Here, we attempted to modify the original R3C ribozyme (73 nucleotides) by reducing the number of nucleotides while maintaining the maximum possible catalytic efficiency. By partially deleting both the "grip" (P4 + P5) and "hammer" (P3) stem-loops, we found the critical border to retain activity comparable to that of full-length R3C. The three-way junction structure was necessary to maintain enzymatic function and the stability of the "grip" (P4 + P5) stem had a large influence on the catalytic activity of R3C. The final minimized ribozyme we obtained comprised ~50 nucleotides, comparable to the estimated length of prebiotically synthesized RNA. Our findings suggest that the autocatalytic function in ribozymes is indeed possible to obtain using sequence lengths achievable with prebiotic synthesis.
R3C连接酶核酶是一种通过对缺乏胞苷的核酶进行修饰而产生的人工连接酶核酶。在此,我们试图通过减少核苷酸数量同时保持最大可能的催化效率来修饰原始的R3C核酶(73个核苷酸)。通过部分删除“夹子”(P4 + P5)和“锤头”(P3)茎环,我们找到了保留与全长R3C相当活性的关键界限。三向接头结构对于维持酶功能是必需的,并且“夹子”(P4 + P5)茎的稳定性对R3C的催化活性有很大影响。我们最终获得的最小化核酶包含约50个核苷酸,与益生元合成RNA的估计长度相当。我们的研究结果表明,使用益生元合成可实现的序列长度确实有可能获得核酶中的自催化功能。