Biochemical analysis of hatchet self-cleaving ribozymes

被引:24
|
作者
Li, Sanshu [1 ,2 ]
Luense, Christina E. [2 ]
Harris, Kimberly A. [1 ,2 ]
Breaker, Ronald R. [1 ,2 ,3 ]
机构
[1] Yale Univ, Howard Hughes Med Inst, New Haven, CT 06520 USA
[2] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
[3] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
基金
美国国家卫生研究院;
关键词
comparative sequence analysis; phosphoester transfer; phosphorothioate; RNA processing; RNA cleavage; CLEAVAGE REACTION; STRUCTURAL BASIS; RNA CLEAVAGE; STABILITY; SPEED; CATALYSIS; KINETICS; SITE;
D O I
10.1261/rna.052522.115
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
Hatchet RNAs are members of a novel self-cleaving ribozyme class that was recently discovered by using a bioinformatics search strategy. The consensus sequence and secondary structure of this class includes 13 highly conserved and numerous other modestly conserved nucleotides interspersed among bulges linking four base-paired substructures. A representative hatchet ribozyme from a metagenomic source requires divalent ions such as Mg2+ to promote RNA strand scission with a maximum rate constant of similar to 4 min(-1). As with all other small self-cleaving ribozymes discovered to date, hatchet ribozymes employ a general mechanism for catalysis involving the nucleophilic attack of a ribose 2'-oxygen atom on an adjacent phosphorus center. Kinetic characteristics of the reaction demonstrate that members of this ribozyme class have an essential requirement for divalent metal ions and that they might have a complex active site that employs multiple catalytic strategies to accelerate RNA cleavage by internal phosphoester transfer.
引用
收藏
页码:1845 / 1851
页数:7
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