清脆的
生物
基因组编辑
基因组工程
计算生物学
基因组
DNA连接酶
同源定向修复
DNA
DNA修复
遗传学
基因
DNA错配修复
作者
Ujjayinee Ray,Supriya V. Vartak,Sathees C. Raghavan
出处
期刊:Gene
[Elsevier]
日期:2020-08-09
卷期号:763: 144997-144997
被引量:12
标识
DOI:10.1016/j.gene.2020.144997
摘要
The CRISPR-Cas system currently stands as one of the best multifaceted tools for site-specific genome engineering in mammals. An important aspect of research in this field focusses on improving the specificity and efficacy of precise genome editing in multiple model systems. The cornerstone of this mini-review is one of the extensively investigated small molecule inhibitor, SCR7, which abrogates NHEJ, a Ligase IV-dependent DSB repair pathway, thus guiding integration of the foreign DNA fragment via the more precise homology directed repair during genome editing. One of our recent studies sheds light on properties of different forms of SCR7. Here, we give a succinct account on the use of SCR7 and its different forms in CRISPR-Cas system, highlighting their chemical properties and biological relevance as potent efficiency-enhancing CRISPR tools.
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