The Influence of Arm Length Asymmetry and Base Substitution on the Activity of the 10-23 DNA Enzyme
Autor: | Murray J. Cairns, Toni M. Hopkins, Craig Witherington, Lun-Quan Sun |
---|---|
Rok vydání: | 2000 |
Předmět: |
Stereochemistry
Base pair Genes myc Deoxyribozyme DNA Single-Stranded Transfection Cleavage (embryo) Cell Line Substrate Specificity chemistry.chemical_compound Nucleic acid thermodynamics Genetics Animals Nucleotide Base Pairing Gene Pharmacology chemistry.chemical_classification Oligoribonucleotides Base Sequence Chemistry Nucleic Acid Hybridization RNA Muscle Smooth DNA Catalytic Rats Kinetics Oligodeoxyribonucleotides Biochemistry Mutation Nucleic Acid Conformation Thermodynamics Electrophoresis Polyacrylamide Gel Cell Division DNA |
Zdroj: | Antisense and Nucleic Acid Drug Development. 10:323-332 |
ISSN: | 1087-2906 |
DOI: | 10.1089/oli.1.2000.10.323 |
Popis: | A small oligodeoxyribonucleotide derived from in vitro selection has been shown to be capable of efficient sequence-specific cleavage of RNA at purine-pyrimidine junctions. As the reaction readily takes place under simulated physiologic conditions, this molecule described as the 10-23 general purpose RNA-cleaving DNA enzyme, has potential as a therapeutic agent. To further explore the character of this prototype, we examined the influence of base substitution and binding arm length asymmetry on its RNA cleaving activity. Surprisingly, substitution of the proximal nucleotide on the 3'-arm, to allow nonstandard Watson-Crick interactions, was found in some instances to improve the cleavage reaction rate. Although the identity of the unpaired purine in the RNA substrate cleavage site was found to have only a subtle influence on the rate of catalysis, with a slight decrease observed when a G at this position was changed to an A, nucleotide substitution (G to C) in the core motif at position 14 was found to completely abolish catalysis. The effect of arm length reduction varied with RNA substrate sequence and extent of helix asymmetry. Where the cleavage rate of one substrate was impaired by truncation of the deoxyribozymes 5'-arm (6 bp), the same modification in reactions with a different sequence produced a rate enhancement. Truncation of the 3'-arm, however, had no effect on the reaction rate of the one substrate tested yet nearly halved the cleavage rate in another substrate. |
Databáze: | OpenAIRE |
Externí odkaz: |