Biochemical analysis of pistol self-cleaving ribozymes

被引:46
作者
Harris, Kimberly A. [1 ,2 ]
Luense, Christina E. [2 ]
Li, Sanshu [1 ,2 ]
Brewer, Kenneth I. [3 ]
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; RNA; SPEED; SITE;
D O I
10.1261/rna.052514.115
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
Pistol RNAs are members of a distinct class of self-cleaving ribozymes that was recently discovered by using a bioinformatics search strategy. Several hundred pistol ribozymes share a consensus sequence including 10 highly conserved nucleotides and many other modestly conserved nucleotides associated with specific secondary structure features, including three base-paired stems and a pseudoknot. A representative pistol ribozyme from the bacterium Lysinibacillus sphaericus was found to promote RNA strand scission with a rate constant of similar to 10 min(-1) under physiological Mg2+ and pH conditions. The reaction proceeds via the nucleophilic attack of a 2'-oxygen atom on the adjacent phosphorus center, and thus adheres to the same general catalytic mechanism of internal phosphoester transfer as found with all other classes of natural self-cleaving ribozymes discovered to date. Analyses of the kinetic characteristics and the metal ion requirements of the cleavage reaction reveal that members of this ribozyme class likely use several catalytic strategies to promote the rapid cleavage of RNA.
引用
收藏
页码:1852 / 1858
页数:7
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