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Nucleosomes Selectively Inhibit Cas9 Off-target Activity at a Site Located at the Nucleosome Edge

机译:核小体在位于核小体边缘的位点选择性抑制Cas9脱靶活性。

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摘要

Nucleosomes affect Cas9 binding and activity at on-target sites, but their impact at off-target sites is unknown. To investigate how nucleosomes affect Cas9 cleavage at off-target sites in vitro, we used a single guide RNA (sgRNA) that has been previously shown to efficiently direct Cas9 cleavage at the edge of the strongly positioned 601 nucleosome. Our data indicate that single mismatches between the sgRNA and DNA target have relatively little effect on Cas9 cleavage of naked DNA substrates, but strongly inhibit cleavage of nucleosome substrates, particularly when the mismatch is in the sgRNA “seed” region. These findings indicate that nucleosomes may enhance Cas9 specificity by inhibiting cleavage of off-target sites at the nucleosome edge.
机译:核小体会影响Cas9结合和在靶位点上的活性,但它们对靶外位点的影响尚不清楚。为了研究核小体如何在体外影响脱靶位点的Cas9裂解,我们使用了单个向导RNA(sgRNA),该RNA先前已被证明可以有效地将Cas9裂解直接引导至强定位的601核小体的边缘。我们的数据表明,sgRNA和DNA靶标之间的单个错配对裸DNA底物的Cas9裂解影响相对较小,但强烈抑制核小体底物的裂解,尤其是当错配位于sgRNA“种子”区域时。这些发现表明,核小体可以通过抑制核小体边缘脱靶位点的切割来增强Cas9特异性。

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