Seamless genome editing in mammalian cells using CRISPR-Cas9 system
Genome editing is valuable for understanding gene function and for gene therapy.But the rate of traditionally homologous recombination is very low and the Cre/loxP leaves behind a 34bp sequence together with the targeted mutation and the transposase can reintegrate the released piggyBac into other chromosomal sites.Here we presented a seamless strategy for editing CCR5 gene using the CRISPR-Cas9 system twice based on the HR and SSA repair mechanism respectively.
Yichun Bai Linjie He Kun Xu Zhiying Zhang
Northwest A&F University, Yangling, shaanxi, 712100, China
国内会议
陕西杨凌
英文
29-30
2015-12-23(万方平台首次上网日期,不代表论文的发表时间)