CRISPR-Cas: biology, mechanisms and relevance

被引:239
|
作者
Hille, Frank [1 ]
Charpentier, Emmanuelle [1 ,2 ]
机构
[1] Max Planck Inst Infect Biol, Dept Regulat Infect Biol, D-10117 Berlin, Germany
[2] Umea Univ, Dept Mol Biol, UCMR, Lab Mol Infect Med Sweden MIMS, S-90187 Umea, Sweden
基金
瑞典研究理事会;
关键词
CRISPR; Cas9; bacteriophage; genome editing; MYXOCOCCUS-XANTHUS DEVELOPMENT; SEQUENCE-SPECIFIC CONTROL; HORIZONTAL GENE-TRANSFER; STRAND BREAK REPAIR; PROCESSES PRE-CRRNA; ESCHERICHIA-COLI; SPACER ACQUISITION; IMMUNE-SYSTEM; RNA CLEAVAGE; MYCOBACTERIUM-TUBERCULOSIS;
D O I
10.1098/rstb.2015.0496
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Prokaryotes have evolved several defence mechanisms to protect themselves from viral predators. Clustered regularly interspaced short palindromic repeats (CRISPR) and their associated proteins (Cas) display a prokaryotic adaptive immune system that memorizes previous infections by integrating short sequences of invading genomes-termed spacers-into the CRISPR locus. The spacers interspaced with repeats are expressed as small guide CRISPR RNAs (crRNAs) that are employed by Cas proteins to target invaders sequence-specifically upon a reoccurring infection. The ability of the minimal CRISPR-Cas9 system to target DNA sequences using programmable RNAs has opened new avenues in genome editing in a broad range of cells and organisms with high potential in therapeutical applications. While numerous scientific studies have shed light on the biochemical processes behind CRISPR-Cas systems, several aspects of the immunity steps, however, still lack sufficient understanding. This review summarizes major discoveries in the CRISPR-Cas field, discusses the role of CRISPR-Cas in prokaryotic immunity and other physiological properties, and describes applications of the system as a DNA editing technology and antimicrobial agent. This article is part of the themed issue 'The new bacteriology'.
引用
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页数:12
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