基因组编辑
清脆的
生物
基因组
计算生物学
遗传学
染色体易位
Cas9
DNA
基因
作者
Grégoire Cullot,Eric J. Aird,Moritz F. Schlapansky,Charles D. Yeh,Lilly van de Venn,Iryna Vykhlyantseva,Susanne Kreutzer,Dominic Mailänder,Bohdan Lewków,Julia Klermund,Christian Montellese,Martina Biserni,Florian Aeschimann,Cédric Vonarburg,Helmuth Gehart,Toni Cathomen,Jacob E. Corn
标识
DOI:10.1038/s41587-024-02488-6
摘要
Abstract The DNA-PKcs inhibitor AZD7648 enhances CRISPR–Cas9-directed homology-directed repair efficiencies, with potential for clinical utility, but its possible on-target consequences are unknown. We found that genome editing with AZD7648 causes frequent kilobase-scale and megabase-scale deletions, chromosome arm loss and translocations. These large-scale chromosomal alterations evade detection through typical genome editing assays, prompting caution in deploying AZD7648 and reinforcing the need to investigate multiple types of potential editing outcomes.
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