Generation of a catalytic module on a self-folding RNA

被引:19
作者
Yoshioka, W
Ikawa, Y
Jaeger, L
Shiraishi, H
Inoue, T [1 ]
机构
[1] Kyoto Univ, Grad Sch Biostudies, Kyoto 6068502, Japan
[2] Kyoto Univ, Grad Sch Sci, Kyoto 6068502, Japan
[3] Univ Calif San Bernadino, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
关键词
catalytic RNA; in vitro selection; ligation;
D O I
10.1261/rna.7170304
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
It is theoretically possible to obtain a catalytic site of an artificial ribozyme from a random sequence consisting of a limited numbers of nucleotides. However, this strategy has been inadequately explored. Here, we report an in vitro selection technique that exploits modular construction of a structurally constrained RNA to acquire a catalytic site for RNA ligation from a short random sequence. To practice the selection, a sequence of 30 nucleotides was located close to the putative reaction site in a derivative of a naturally occurring self-folding RNA whose crystal structure is known. RNAs whose activity depended on the starting three-dimensional structure were selected with 3'-5' ligation specificity, indicating that the strategy can be used to acquire a variety of catalytic sites and other functional RNA modules.
引用
收藏
页码:1900 / 1906
页数:7
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