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Nuclease Target Site Selection for Maximizing On-target Activity and Minimizing Off-target Effects in Genome Editing

机译:核酸酶靶位点选择,可在基因组编辑中最大化靶标活性并最小化脱靶效应

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摘要

The rapid advancement in targeted genome editing using engineered nucleases such as ZFNs, TALENs, and CRISPR/Cas9 systems has resulted in a suite of powerful methods that allows researchers to target any genomic locus of interest. A complementary set of design tools has been developed to aid researchers with nuclease design, target site selection, and experimental validation. Here, we review the various tools available for target selection in designing engineered nucleases, and for quantifying nuclease activity and specificity, including web-based search tools and experimental methods. We also elucidate challenges in target selection, especially in predicting off-target effects, and discuss future directions in precision genome editing and its applications.
机译:使用诸如ZFNs,TALENs和CRISPR / Cas9等工程核酸酶的靶向基因组编辑的快速发展,产生了一套强大的方法,可让研究人员靶向任何感兴趣的基因组位点。已开发出一套辅助设计工具,以协助研究人员进行核酸酶设计,目标位点选择和实验验证。在这里,我们回顾了可用于设计工程核酸酶的目标选择以及定量核酸酶活性和特异性的各种工具,包括基于Web的搜索工具和实验方法。我们还阐明了靶标选择中的挑战,尤其是预测脱靶效应的挑战,并讨论了精确基因组编辑及其应用的未来方向。

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