CRISPR-Cas9介导的基因组编辑技术的研究进展附视频

被引:24
作者
郑小梅 [1 ,2 ]
张晓立 [1 ,3 ]
于建东 [1 ,2 ]
郑平 [1 ,2 ]
孙际宾 [1 ,2 ]
机构
[1] 中国科学院系统微生物工程重点实验室
[2] 中国科学院天津工业生物技术研究所
[3] 天津科技大学生物工程学院
关键词
CRISPR-Cas系统; Cas9; 基因组编辑技术;
D O I
暂无
中图分类号
Q811.4 [生物信息论];
学科分类号
0711 ; 0831 ;
摘要
CRISPR-Cas(clustered regularly interspaced short palindromic repeats-CRISPR-associated proteins)系统为细菌与古生菌中抵御外源病毒或质粒DNA入侵的获得性免疫系统。该系统在crRNA的指导下,使核酸酶Cas识别并降解外源DNA。其中,Ⅱ型CRISPR-Cas系统最为简单,仅包括一个核酸酶Cas9与tracrRNA:crRNA二聚体便可完成其生物功能。基于CRISPR-Cas9的基因组编辑技术的核心为将tracrRNA:crRNA设计为引导RNA,在引导RNA的指导下Cas9定位于特定DNA序列上,进行DNA双链切割,实现基因组的定向编辑。CRISPR-Cas9系统以设计操纵简便、编辑高效与通用性广等优势成为新一代基因组编辑技术,为基因组定向改造调控与应用等带来突破性革命。从CRISPR-Cas9介导的基因组编辑技术的发展与应用等方面综述其最新研究进展,并着重介绍该技术的关键影响因素,为相关研究者提供参考。
引用
收藏
页码:1 / 9+78 +78-79
页数:11
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