A comparison of multiple shRNA expression methods for combinatorial RNAi.

Glen J McIntyre, Allison J Arndt, Kirsten M Gillespie, Wendy M Mak, Gregory C Fanning
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引用次数: 23

Abstract

RNAi gene therapies for HIV-1 will likely need to employ multiple shRNAs to counter resistant strains. We evaluated 3 shRNA co-expression methods to determine their suitability for present use; multiple expression vectors, multiple expression cassettes and single transcripts comprised of several dsRNA units (aka domains) with each being designed to a different target. Though the multiple vector strategy was effective with 2 shRNAs, the increasing number of vectors required is a major shortcoming. With single transcript configurations we only saw adequate activity from 1 of 10 variants tested, the variants being comprised of 2 - 3 different target domains. Whilst single transcript configurations have the most advantages on paper, these configurations can not yet be rapidly and reliably re-configured for new targets. However, our multiple cassette combinations of 2, 3 and 4 (29 bp) shRNAs were all successful, with suitable activity maintained in all positions and net activities comparable to that of the corresponding single shRNAs. We conclude that the multiple cassette strategy is the most suitably developed for present use as it is easy to design, assemble, is directly compatible with pre-existing shRNA and can be easily expanded.

Abstract Image

Abstract Image

Abstract Image

用于组合RNAi的多种shRNA表达方法的比较。
HIV-1的RNAi基因治疗可能需要使用多种shRNA来对抗耐药菌株。我们评估了3种shRNA共表达方法,以确定它们是否适合目前的用途;多个表达载体、多个表达盒和由多个dsRNA单元(又名结构域)组成的单个转录物,每个dsRNA单元被设计成不同的靶标。尽管多载体策略对2个shRNA是有效的,但所需载体数量的增加是一个主要缺点。对于单转录物配置,我们只从测试的10个变体中的1个变体中看到了足够的活性,这些变体由2-3个不同的靶结构域组成。虽然单转录物配置在纸面上具有最大优势,但这些配置还不能快速可靠地为新目标重新配置。然而,我们的2、3和4(29bp)shRNA的多个盒组合都是成功的,在所有位置都保持了合适的活性,净活性与相应的单个shRNA相当。我们得出的结论是,多盒策略是最适合目前使用的策略,因为它易于设计、组装,与预先存在的shRNA直接兼容,并且可以轻松扩展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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