Journal
RNA
Volume 21, Issue 11, Pages 1852-1858Publisher
COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1261/rna.052514.115
Keywords
comparative sequence analysis; phosphoester transfer; phosphorothioate; RNA processing; RNA cleavage
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Funding
- National Institutes of Health [GM022778, T32-HG 003198]
- Howard Hughes Medical Institute
- Deutsche Forschungsgemeinschaft [LU1889/1-1]
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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.
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