清脆的
Cas9
核酸酶
计算生物学
基因组编辑
生物
遗传学
DNA
基因
作者
Julian Boutin,David Cappellen,J. Rosier,Samuel Amintas,Sandrine Dabernat,Aurélie Bedel,François Moreau‐Gaudry
标识
DOI:10.1089/crispr.2021.0120
摘要
CRISPR-Cas9 is a highly promising technology for clinical development. However, this powerful tool can induce adverse genomic events. The off-target genotoxicity is well described, predictable, detectable, and resolved by the use of new generations of Cas9 nucleases with high fidelity. In contrast, the ON-target genotoxicity due to a DNA double-strand break at the targeted locus is still underestimated. Here, we review several genomic outcomes induced by CRISPR-Cas9 from the insertion/deletion of a few bases to megabase-scale rearrangements. We hope to highlight this barely detectable complex safety concern to promote further studies to understand the mechanisms better, to detect these unwanted events, and to prevent them for the safety management of future CRISPR-Cas9 clinical trials.
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