Repair of a Site-Specific DNA Cleavage: Old-School Lessons for Cas9-Mediated Gene Editing.

Repair of a Site-Specific DNA Cleavage: Old-School Lessons for Cas9-Mediated Gene Editing.
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DOI:
10.1021/acschembio.7b00760
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发表时间:
2018-02-16
影响因子:
4
通讯作者:
Haber JE
Haber JE
中科院分区:
生物学2区
文献类型:
--
作者:
Gallagher DN;Haber JE

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CRISPR/Cas9介导的基因编辑可以涉及非同源末端连接以产生各种插入/缺失(indel),或者可以采用同源重组以精确地修饰靶DNA序列。我们对这些过程的理解是由早期使用其他位点特异性核酸内切酶的研究指导的,无论是在模式生物如芽殖酵母还是在哺乳动物细胞中。我们简要回顾了使用HO和I-SceI核酸内切酶从这些研究中收集到的信息,以及这些发现如何指导当前的基因编辑策略。
CRISPR/Cas9-mediated gene editing may involve nonhomologous end-joining to create various insertion/deletions (indels) or may employ homologous recombination to modify precisely the target DNA sequence. Our understanding of these processes has been guided by earlier studies using other site-specific endonucleases, both in model organisms such as budding yeast and in mammalian cells. We briefly review what has been gleaned from such studies using the HO and I-SceI endonucleases and how these findings guide current gene editing strategies.
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