Museum National d'Histoire Naturelle, INSERM U1154, CNRS UMR 7196, Sorbonne Universités, 43 rue Cuvier, Paris, F-75231, France.
Translational Sciences, Sanofi, 13 Quai Jules Guesde, F-94400, Vitry-sur-Seine, France.
Nat Commun. 2018 Mar 19;9(1):1133. doi: 10.1038/s41467-018-03475-7.
In genome editing with CRISPR-Cas9, transgene integration often remains challenging. Here, we present an approach for increasing the efficiency of transgene integration by homology-dependent repair (HDR). CtIP, a key protein in early steps of homologous recombination, is fused to Cas9 and stimulates transgene integration by HDR at the human AAVS1 safe harbor locus. A minimal N-terminal fragment of CtIP, designated HE for HDR enhancer, is sufficient to stimulate HDR and this depends on CDK phosphorylation sites and the multimerization domain essential for CtIP activity in homologous recombination. HDR stimulation by Cas9-HE, however, depends on the guide RNA used, a limitation that may be overcome by testing multiple guides to the locus of interest. The Cas9-HE fusion is simple to use and allows obtaining twofold or more efficient transgene integration than that with Cas9 in several experimental systems, including human cell lines, iPS cells, and rat zygotes.
在 CRISPR-Cas9 基因编辑中,转基因整合通常仍然具有挑战性。在这里,我们提出了一种通过同源依赖性修复(HDR)来提高转基因整合效率的方法。CtIP 是同源重组早期步骤中的关键蛋白,它与 Cas9 融合,并通过 HDR 在人类 AAVS1 安全港基因座刺激转基因整合。CtIP 的最小 N 端片段,命名为 HDR 增强子(HE),足以刺激 HDR,这取决于 CDK 磷酸化位点和多聚化结构域,这些结构域对于同源重组中 CtIP 的活性是必需的。然而,Cas9-HE 通过 HDR 的刺激取决于所用的向导 RNA,这一限制可以通过测试多个导向感兴趣基因座的向导 RNA 来克服。Cas9-HE 融合物易于使用,并且在几种实验系统中,包括人细胞系、iPS 细胞和大鼠受精卵,比 Cas9 获得了两倍或更高效率的转基因整合。