The use of 10-23 DNAzyme to selectively destroy the allele of mRNA with a unique purine-pyrimidine dinucleotide.

Tong-Hong Wang, Wan-Ting Li, Szu-Hsien Yu, Lo-Chun Au
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引用次数: 14

Abstract

10-23 DNAzyme is an oligodeoxyribonucleotide-based ribonuclease. It consists of a 15-nt catalytic domain flanked by two target-specific complementary arms. It has been shown to cleave target mRNA effectively at purine (R)-pyrimidine (Y) dinucleotide. Taking advantage of this specific property, 10-23 DNAzyme was designed to cleave mRNA of a given allele at a unique RY dinucleotide while leaving the mRNA encoded from other alleles of the same gene intact. In this study, a p53-R249S (AGG-->AGT) mutant was tested. 10-23 DNAzyme was used to cut mutant mRNA at GT dinucleotide of codon 249. Both in vitro and in vivo studies showed that this DNAzyme could specifically cut the mutant p53 allele, leaving the wild-type unaffected. This proof-of-concept experiment provided a new way to knock down expression of a given allele with special single-base transversion.

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利用10-23 DNAzyme选择性地破坏具有独特嘌呤嘧啶二核苷酸的mRNA等位基因。
10- 23dnazyme是一种基于寡脱氧核糖核苷酸的核糖核酸酶。它由一个15-nt催化结构域和两个靶向互补臂组成。它已被证明在嘌呤(R)-嘧啶(Y)二核苷酸上有效地切割目标mRNA。利用这一特性,10-23 DNAzyme被设计成在一个独特的RY二核苷酸上切割给定等位基因的mRNA,同时保持同一基因的其他等位基因编码的mRNA完整。本研究检测了p53-R249S (AGG- >AGT)突变体。10-23 DNAzyme用于切割密码子249 GT二核苷酸处的突变mRNA。体外和体内研究都表明,这种DNAzyme可以特异性地切割突变的p53等位基因,而不影响野生型。这个概念验证实验提供了一种新的方法,通过特殊的单碱基翻转来敲低给定等位基因的表达。
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Oligonucleotides
Oligonucleotides 生物-生化与分子生物学
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