Pellenz Stefan, Monnat Raymond J
Department of Pathology, University of Washington, Seattle, WA, USA.
Methods Mol Biol. 2014;1123:245-64. doi: 10.1007/978-1-62703-968-0_16.
Homing endonucleases (HEs) are highly site-specific enzymes that enable genome engineering by introducing DNA double-strand breaks (DSB) in genomic target sites. DSB repair from an HE-induced DSB can promote target site gene deletion, mutation, or gene addition, depending on the experimental protocol. In this chapter we outline how to identify potential genomic target sites for HEs with known target site specificities and the different experimental strategies that can be used to assess site cleavage in living cells. As an example of this approach, we identify potential human genomic target sites for the LAGLIDADG HE I-CreI that, by nine different selection criteria, may be new "safe harbor" sites for gene insertion.
归巢内切酶(HEs)是高度位点特异性的酶,可通过在基因组靶位点引入DNA双链断裂(DSB)来实现基因组工程。根据实验方案,由HE诱导的DSB进行的DSB修复可促进靶位点基因缺失、突变或基因添加。在本章中,我们概述了如何识别具有已知靶位点特异性的HEs的潜在基因组靶位点,以及可用于评估活细胞中位点切割的不同实验策略。作为这种方法的一个例子,我们确定了LAGLIDADG HE I-CreI的潜在人类基因组靶位点,根据九个不同的选择标准,这些位点可能是基因插入的新“安全港”位点。