清脆的
基因组编辑
Cas9
工具箱
计算生物学
基因组工程
亚基因组mRNA
基因组
生物
计算机科学
合成生物学
基因
遗传学
程序设计语言
作者
Xiaofeng Dai,Xiao Chen,Qiuwu Fang,Jia Li,Zhonghu Bai
标识
DOI:10.1080/07388551.2017.1378999
摘要
The discovery of CRISPR–Cas9/dCas9 system has reinforced our ability and revolutionized our history in genome engineering. While Cas9 and dCas9 are programed to modulate gene expression by introducing DNA breaks, blocking transcription factor recruitment or dragging functional groups towards the targeted sites, sgRNAs determine the genomic loci where the modulation occurs. The off-target problem, due to limited sgRNA specificity and genome complexity of many species, has posed concerns for the wide application of this revolutionary technique. To solve this problem and, more importantly, gain power over gene functionality and cell fate control, inducible strategies have been continuously evolved to offer tailored solutions to address specific biological questions. By reviewing recent advances in inducible CRISPR system design and critical elements potentially adding values to such systems, we classify current approaches in this domain into four mechanically distinct categories, namely, "split system", "allosteric system", "combinatorial system", and "transient delivery system", discuss the pros and cons of each system, and point out the under-explored areas and future directions, with the aim of enriching our toolbox of delicate life engineering.
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