Cas9-Assisted Targeting of CHromosome segments CATCH enables one-step targeted cloning of large gene clusters

被引:209
作者
Jiang, Wenjun [1 ]
Zhao, Xuejin [2 ]
Gabrieli, Tslil [3 ]
Lou, Chunbo [2 ]
Ebenstein, Yuval [3 ]
Zhu, Ting F. [1 ]
机构
[1] Tsinghua Univ, MOE Key Lab Bioinformat, Sch Life Sci,Ctr Synthet & Syst Biol, Collaborat Innovat Ctr Diag & Treatment Infect Di, Beijing 100084, Peoples R China
[2] Chinese Acad Sci, Inst Microbiol, CAS Key Lab Microbial Physiol & Metab Engn, Beijing 100101, Peoples R China
[3] Tel Aviv Univ, Raymond & Beverly Sackler Fac Exact Sci, Sch Chem, IL-6997801 Tel Aviv, Israel
基金
欧洲研究理事会; 以色列科学基金会; 中国国家自然科学基金;
关键词
ESCHERICHIA-COLI; CRISPR/CAS SYSTEM; HUMAN-CELLS; IN-VITRO; DNA; CAS9; BIOSYNTHESIS; SPECIFICITY; COMPLEX; BACTERIOPHAGE;
D O I
10.1038/ncomms9101
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The cloning of long DNA segments, especially those containing large gene clusters, is of particular importance to synthetic and chemical biology efforts for engineering organisms. While cloning has been a defining tool in molecular biology, the cloning of long genome segments has been challenging. Here we describe a technique that allows the targeted cloning of near-arbitrary, long bacterial genomic sequences of up to 100 kb to be accomplished in a single step. The target genome segment is excised from bacterial chromosomes in vitro by the RNA-guided Cas9 nuclease at two designated loci, and ligated to the cloning vector by Gibson assembly. This technique can be an effective molecular tool for the targeted cloning of large gene clusters that are often expensive to synthesize by gene synthesis or difficult to obtain directly by traditional PCR and restriction-enzyme-based methods.
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页数:8
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