Bulletin of the Korean chemical society | |
Efficient Target Site Selection for an RNA-cleaving DNAzyme through Combinatorial Library Screening | |
Ki-Sun Kim1  Soo-Jeong Gong1  Dong-Eun Kim1  Sangtaek Oh1  Woo-Hyung Choi1  Jae Hyun Kim1  | |
关键词: Antisense oligonucleotide; 10-23 DNAzyme; DNAzyme library; Gene inactivation; RNA cleavage; | |
DOI : | |
学科分类:化学(综合) | |
来源: Korean Chemical Society | |
【 摘 要 】
Identification of accessible sites in targeted RNAs is a major limitation to the effectiveness of antisense oligonucleotides. A class of antisense oligodeoxynucleotides, known as the �?10-23�? DNA enzyme or DNAzyme, which is a small catalytic DNA, has been shown to efficiently cleave target RNA at purinepyrimidine junctions in vitro. We have designed a strategy to identify accessible cleavage sites in the target RNA, which is hepatitis C virus nonstructural gene 3 (HCV NS3) RNA that encodes viral helicase and protease, from a pool of random DNAzyme library. A pool of DNAzymes of 58 nucleotides-length that possess randomized annealing arms, catalytic core sequence, and fixed 5`/3`-end flanking sequences was designed and screened for their ability to cleave the target RNA. The screening procedure, which includes binding of DNAzyme pool to the target RNA under inactive condition, selection and amplification of active DNAzymes, incubation of the selected DNAzymes with the target RNA, and target site identification on sequencing gels, identified 16 potential cleavage sites in the target RNA. Corresponding DNAzymes were constructed for the selected target sites and were tested for RNA-cleavage in terms of kinetics and accessibility. These selected DNAzymes were effective in cleaving the target RNA in the presence of Mg2+. This strategy can be applicable to identify accessible sites in any target RNA for antisense oligonucleotides-based gene inactivation methods.
【 授权许可】
Unknown
【 预 览 】
Files | Size | Format | View |
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RO201912010240087ZK.pdf | 1320KB | download |