首页> 外文期刊>Nucleic Acids Research >Light-activated RNA interference using double-stranded siRNA precursors modified using a remarkable regiospecificity of diazo-based photolabile groups.
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Light-activated RNA interference using double-stranded siRNA precursors modified using a remarkable regiospecificity of diazo-based photolabile groups.

机译:使用双链siRNA前体进行光激活的RNA干扰,该双链siRNA前体使用基于重氮基的光不稳定基团的显着区域特异性进行修饰。

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摘要

Diazo-based precursors of photolabile groups have been used extensively for modifying nucleic acids, with the intention of toggling biological processes with light. These processes include transcription, translation and RNA interference. In these cases, the photolabile groups have been typically depicted as modifying the phosphate backbone of RNA and DNA. In this work we find that these diazo-based reagents in fact react very poorly with backbone phosphates. Instead, they show a remarkable specificity for terminal phosphates and very modest modification of the nucleobases. Furthermore, the photo deprotection of these terminal modifications is shown to be much more facile than nucleobase modified sites. In this study we have characterized this regiospecificity using RNA duplexes and model nucleotides, analyzed using LC/MS/MS. We have also applied this understanding of the regio-specificity to our technique of light activated RNA interference (LARI). We examined 27-mer double-stranded precursors of siRNA ('dsRNA'), and have modified them using the photo-cleavable di-methoxy nitro phenyl ethyl group (DMNPE) group. By incorporating terminal phosphates in the dsRNA, we are able to guide DMNPE to react at these terminal locations. These modified dsRNA duplexes show superior performance to our previously described DMNPE-modified siRNA, with the range of expression that can be toggled by light increasing by a factor of two.
机译:光不稳定基团的基于重氮基的前体已广泛用于修饰核酸,目的是用光来切换生物过程。这些过程包括转录,翻译和RNA干扰。在这些情况下,光不稳定基团通常被描述为修饰RNA和DNA的磷酸骨架。在这项工作中,我们发现这些重氮基试剂实际上与骨架磷酸酯的反应非常差。相反,它们对末端磷酸盐显示出显着的特异性,并且对核碱基的修饰非常适度。此外,显示出这些末端修饰的光脱保护比核碱基修饰的位点容易得多。在这项研究中,我们使用RNA双链体和模型核苷酸表征了这种区域特异性,并使用LC / MS / MS分析了该核苷酸。我们还将对区域特异性的理解应用于我们的光活化RNA干扰(LARI)技术。我们检查了27-mer siRNA的双链前体('dsRNA'),并使用可光裂解的二甲氧基硝基苯基乙基(DMNPE)基团对其进行了修饰。通过在dsRNA中掺入末端磷酸酯,我们能够指导DMNPE在这些末端位置反应。这些修饰的dsRNA双链体表现出比我们先前描述的DMNPE修饰的siRNA优越的性能,可被光触发的表达范围增加了两倍。

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