Johnson and Johnson Research Pty Ltd, Level 4 Biomedical Building, 1 Central Avenue, Australian Technology Park, Eveleigh, NSW, 1430, Australia.
BMC Mol Biol. 2011 Aug 8;12:34. doi: 10.1186/1471-2199-12-34.
Expressed short hairpin RNAs (shRNA) used in mammalian RNA interference (RNAi) are often designed around a specific short interfering RNA (siRNA) core. Whilst there are algorithms to aid siRNA design, hairpin-specific characteristics such as stem-length and siRNA core placement within the stem are not well defined.
Using more than 91 hairpins designed against HIV-1 Tat and Vpu, we investigated the influence of both of these factors on suppressive activity, and found that stem length does not correspond with predictable changes in suppressive activity. We also detected multiple processed products for all stem lengths tested. However, the entire length of the hairpin stem was not equally processed into active products. As such, the placement of the siRNA core at the base terminus was critical for activity.
We conclude that there is no fixed correlation between stem length and suppressive activity. Instead, core selection and placement likely have a greater influence on the effectiveness of shRNA-based silencing.
哺乳动物 RNA 干扰 (RNAi) 中使用的表达短发夹 RNA (shRNA) 通常围绕特定的短干扰 RNA (siRNA) 核心设计。虽然有算法可以辅助 siRNA 设计,但发夹特有的特征,如茎长和 siRNA 核心在茎内的位置,并没有得到很好的定义。
我们使用了超过 91 个针对 HIV-1 Tat 和 Vpu 的发夹进行研究,调查了这两个因素对抑制活性的影响,发现茎长与抑制活性的可预测变化没有对应关系。我们还检测到所有测试茎长的发夹都有多种加工产物。然而,发夹茎的全长并没有被同等地加工成有活性的产物。因此,siRNA 核心在茎末端的位置对于活性至关重要。
我们的结论是,茎长与抑制活性之间没有固定的相关性。相反,核心的选择和位置可能对基于 shRNA 的沉默的有效性有更大的影响。