rnai介导的靶标下调与基因替代的耦合。

Dong-Ho Kim, John J Rossi
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引用次数: 36

摘要

短干扰RNA (siRNA)介导的有害内源性转录物的敲低在遗传性疾病的治疗中具有潜在的应用前景。在突变型和野生型转录本不能被siRNA区分的情况下,可能需要同时用一种对siRNA活性有抗性的修饰形式的靶RNA进行基因替换。为了测试这种可能性,我们利用了一种有效的siRNA来敲除EGFP mRNA。在该系统中,野生型EGFP的表达被siRNA抑制,而在靶区具有密码子修饰的EGFP结构则不会下调。当野生型信息的表达被抑制时,用密码子修饰的EGFP版本转染这些细胞可以同时恢复EGFP的表达。这些研究为用RNA干扰(RNAi)测试这一策略提供了详细的方法和系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Coupling of RNAi-mediated target downregulation with gene replacement.

Short interfering RNA (siRNA)-mediated knockdown of deleterious endogenous transcripts has potential applications for the treatment of hereditary diseases. In situations where the mutant and wildtype transcripts cannot be discriminated from one another by siRNAs, it may be necessary to simultaneously carry out gene replacement with a modified form of the target RNA that is resistant to siRNA activity. To test this possibility, we have taken advantage of a potent siRNA that knocks down EGFP mRNA. In this system, wild-type EGFP expression is suppressed by the siRNA, whereas an EGFP construct with codon modifications in the target region that is otherwise fully functional is not downregulated. When expression of the wild-type message is inhibited, EGFP expression can be simultaneously restored by transfecting these cells with the codon-modified version of EGFP. These studies provide a detailed methodology and system for testing this strategy with RNA interference (RNAi).

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