Institute of Chemical Biology and Fundamental Medicine SB RAS, 630090 Novosibirsk, Russia.
Faculty of Natural Sciences, Novosibirsk State University, 630090 Novosibirsk, Russia.
Int J Mol Sci. 2024 Nov 19;25(22):12392. doi: 10.3390/ijms252212392.
The design of controllable and precise RNA-targeted CRISPR/Cas9 (Clustered Regularly Interspaced Short Palindromic Repeats) systems is an important problem of modern molecular biology and genetic technology. Herein, we have designed a series of photocleavable guide CRISPR RNAs (crRNA) and their 2'-modified (2'-fluoro and locked nucleic acid) analogs containing one or two 1-(2-nitrophenyl)-1,2-ethanediol photolabile linkers (PL). We have demonstrated that these crRNAs can be destroyed by relatively mild UVA irradiation with the rate constants 0.24-0.77 min and that the photocleavage markedly slows down the action of Cas9 nuclease in the model in vitro system. Two PLs provide more rapid crRNA destruction than a single linker. PLs in the crRNA structure improve the specificity of DNA cleavage by Cas9 nuclease for the fully complementary target. The application of photocleavable crRNA in CRISPR/Cas9 genome editing permits the system to be switched off in a spatiotemporally controlled manner, thus alleviating its off-target effects.
设计可控且精确的 RNA 靶向 CRISPR/Cas9(成簇规律间隔短回文重复序列)系统是现代分子生物学和遗传技术的一个重要问题。在此,我们设计了一系列光可裂解的向导 CRISPR RNA(crRNA)及其 2'-修饰(2'-氟和锁核酸)类似物,其中包含一个或两个 1-(2-硝基苯基)-1,2-乙二醇光不稳定连接物(PL)。我们已经证明,这些 crRNA 可以通过相对温和的 UVA 照射进行破坏,其速率常数为 0.24-0.77 分钟,光裂解明显减缓了 Cas9 核酸酶在模型体外系统中的作用。两个 PL 比单个连接物提供更快的 crRNA 破坏。PL 在 crRNA 结构中提高了 Cas9 核酸酶对完全互补靶标 DNA 切割的特异性。光可裂解 crRNA 在 CRISPR/Cas9 基因组编辑中的应用允许以时空控制的方式关闭系统,从而减轻其脱靶效应。