Harnessing CRISPR-Cas9 immunity for genetic engineering

被引:68
作者
Charpentier, Emmanuelle [1 ,2 ,3 ]
Marraffini, Luciano A. [4 ]
机构
[1] Helmholtz Ctr Infect Res, Dept Regulat Infect Biol, D-38124 Braunschweig, Germany
[2] Umea Univ, UCMR, Lab Mol Infect Med Sweden MIMS, Dept Mol Biol, S-90187 Umea, Sweden
[3] Hannover Med Sch, D-30625 Hannover, Germany
[4] Rockefeller Univ, Bacteriol Lab, New York, NY 10065 USA
基金
瑞典研究理事会;
关键词
ANTIVIRAL DEFENSE; DUAL-RNA; DNA; CAS9; REPEATS; COMPLEX; INTERFERENCE; SYSTEM; ACTIVATION; EVOLUTION;
D O I
10.1016/j.mib.2014.07.001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
CRISPR-Cas encodes an adaptive immune system that defends prokaryotes against infectious viruses and plasmids. Immunity is mediated by Cas nucleases, which use small RNA guides (the crRNAs) to specify a cleavage site within the genome of invading nucleic acids. In type II CRISPR-Cas systems, the DNA-cleaving activity is performed by a single enzyme Cas9 guided by an RNA duplex. Using synthetic single RNA guides, Cas9 can be reprogrammed to create specific double-stranded DNA breaks in the genomes of a variety of organisms, ranging from human cells to bacteria, and thus constitutes a powerful tool for genetic engineering. Here we describe recent advancements in our understanding of type II CRISPR-Cas immunity and how these studies led to revolutionary genome editing applications.
引用
收藏
页码:114 / 119
页数:6
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