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sgRNA 序列基序阻碍高效的 CRISPR/Cas9 介导的基因编辑。

sgRNA Sequence Motifs Blocking Efficient CRISPR/Cas9-Mediated Gene Editing.

机构信息

Max Delbrück Center for Molecular Medicine, Berlin, Germany.

Max Delbrück Center for Molecular Medicine, Berlin, Germany.

出版信息

Cell Rep. 2019 Jan 29;26(5):1098-1103.e3. doi: 10.1016/j.celrep.2019.01.024.

Abstract

Cas9 nucleases can be programmed with single guide RNAs (sgRNAs) to mediate gene editing. High CRISPR/Cas9-mediated gene knockout efficiencies are essential for genetic screens and critically depend on the properties of the sgRNAs used. The specificity of an sgRNA is defined by its targeting sequence. Here, we discovered that two short sequence motifs at the 3' end of the targeting sequence are almost exclusively present in inefficient sgRNAs of published sgRNA-activity datasets. By specific knock-in of sgRNA target sequences with or without these motifs and quantitative measurement of knockout efficiency, we show that the presence of these motifs in sgRNAs per se results in a 10-fold reduction of gene knockout frequencies. Mechanistically, the cause of the low efficiency differs between the two motifs. These sequence motifs are relevant for future sgRNA design approaches and studies of Cas9-DNA interactions.

摘要

Cas9 核酸酶可以与单指导 RNA(sgRNA)编程,以介导基因编辑。高的 CRISPR/Cas9 介导的基因敲除效率对于遗传筛选至关重要,并且极大地依赖于所使用的 sgRNA 的性质。sgRNA 的特异性由其靶向序列定义。在这里,我们发现靶向序列 3'端的两个短序列基序几乎专门存在于已发表的 sgRNA 活性数据集的低效 sgRNA 中。通过带有或不带有这些基序的 sgRNA 靶序列的特异性敲入以及对敲除效率的定量测量,我们表明 sgRNA 中存在这些基序本身会导致基因敲除频率降低 10 倍。从机制上讲,这两个基序导致低效率的原因不同。这些序列基序与未来的 sgRNA 设计方法和 Cas9-DNA 相互作用的研究有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eff6/6352712/41ba5987d4aa/fx1.jpg

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