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

Wenjun Jiang, Xuejin Zhao, Tslil Gabrieli, Chunbo Lou, Yuval Ebenstein, Ting F. Zhu*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

221 Scopus citations

Abstract

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.

Original languageEnglish
Article number8101
JournalNature Communications
Volume6
DOIs
StatePublished - 1 Sep 2015

Funding

FundersFunder number
Seventh Framework Programme
Center for Life Sciences
Tsinghua University XIN Center
Marie Curie
Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases
Tsinghua University-Peking University Center for Life Sciences
European Research Council
Ministry of Science and Technology of the People's Republic of China2011CBA00805, 2013CB734001, 2015CB553402
National Natural Science Foundation of China31470532, 31470818
European Commission337830
Israel Science Foundation1902/12

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