甲基转移酶核酶的高通量突变分析

R. Yamagami, Hina Kubota, Emi Kohno, Hiroyuki Hori
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引用次数: 0

摘要

甲基转移酶核糖酶 1(MTR1)是一种通过体外选择从随机 RNA 池中分离出来的催化 RNA。该核糖酶利用 6-甲基鸟嘌呤(m6G)作为甲基基团供体,催化 1-甲基腺苷(m1A)的特异性位点形成。该核糖酶已通过生化和结构分析得到广泛表征。在这里,我们描述了对 MTR1 催化结构域单点突变体的高通量筛选,并确定它们对核糖酶活性的影响。我们的突变剖析方法成功地评估了每次实验中测试的 141 个 MTR1 变体的活性,发现核糖酶对催化核心结构域的核苷酸取代非常敏感。我们的技术可用于催化形成不同修饰(如 7-甲基鸟苷(m7G)或 3-甲基胞苷(m3C))的甲基转移核糖酶。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High-throughput mutational analysis of a methyltransferase ribozyme
Methyltransferase ribozyme 1 (MTR1) is a catalytic RNA that has been isolated from a random RNA pool by in vitro selection. The ribozyme catalyzes site-specific formation of 1-methyl adenosine (m1A) using 6-methyl guanine (m6G) as a methyl group donor. The ribozyme has been extensively characterized by biochemical and structural analyses. Here, we describe high-throughput screening of single point mutants in the catalytic domain of MTR1 and determine their effect on ribozyme activity. Our mutational profiling method successfully assessed the activity of the 141 MTR1 variants tested in each experiment and revealed that the ribozyme is very sensitive to nucleotide substitutions in the catalytic core domain. Our technique can be applied to methyltransferase ribozymes that catalyze formation of different modifications such as 7-methylguanosine (m7G) or 3-methylcytidine (m3C).
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