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TARGETED CLEAVAGE OF RNA USING RIBONUCLEASE P TARGETING AND CLEAVAGE SEQUENCES

机译:使用核糖核酸酶P靶向和裂解序列进行RNA靶向裂解

摘要

It has been discovered that any RNA can be targeted for cleavage by RNAase P from eukaryotic cells, for example, human RNAase P, using a suitably designed oligoribonucleotide ("external guide sequence", or EGS) to form a hybrid with the target RNA, thereby creating a substrate for cleavage by RNAase P in vitro. The EGS hydrogen bonds to the targeted RNA to form a partial tRNA like structure including the aminoacyl acceptor stem, the T stem and loop, and part of the D stem. The most efficient EGS with human RNAase P is the EGS in which the anticodon stem and loop was deleted. Modifications can also be made within the T-loop. Methods are also disclosed to randomly select and to express a suitable EGS in vivo to make a selected RNA a target for cleavage by the host cell RNAase P, thus preventing expression of the function of the target RNA. The methods and compositions should be useful to prevent the expression of disease-causing genes in vivo.
机译:已发现,使用适当设计的寡核糖核苷酸(“外部引导序列”或EGS),可将任何RNA靶向RNA酶P切割真核细胞(例如人RNAase P),从而与目标RNA形成杂交体,从而产生了在体外被RNA酶P切割的底物。 EGS氢键结合到目标RNA上,形成部分tRNA样结构,包括氨酰基受体茎,T茎和环以及D茎的一部分。使用人RNAase P的最有效EGS是缺失了反密码子茎和环的EGS。也可以在T环内进行修改。还公开了在体内随机选择并表达合适的EGS以使选择的RNA成为宿主细胞RNA酶P切割的靶标的方法,从而阻止了靶标RNA功能的表达。所述方法和组合物应可用于预防体内致病基因的表达。

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