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Cas9辅助靶向染色体片段技术(CATCH)可实现大型基因簇的一步靶向克隆。

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

作者信息

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

机构信息

School of Life Sciences, Center for Synthetic and Systems Biology, MOE Key Laboratory of Bioinformatics, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Tsinghua University, Beijing 100084, China.

CAS Key Laboratory of Microbial Physiological and Metabolic Engineering, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.

出版信息

Nat Commun. 2015 Sep 1;6:8101. doi: 10.1038/ncomms9101.

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.

摘要

长DNA片段的克隆,尤其是那些包含大型基因簇的片段,对于合成生物学和化学生物学中对生物体进行工程改造的努力而言尤为重要。虽然克隆一直是分子生物学中的一项关键技术,但长基因组片段的克隆却颇具挑战性。在此,我们描述了一种技术,该技术能够在单个步骤中完成长达100 kb的几乎任意长的细菌基因组序列的靶向克隆。目标基因组片段通过RNA引导的Cas9核酸酶在体外从细菌染色体的两个指定位点切除,并通过吉布森组装法连接到克隆载体上。这项技术可以成为一种有效的分子工具,用于靶向克隆大型基因簇,而这些基因簇通过基因合成进行合成通常成本高昂,或者难以通过传统的基于PCR和限制性酶的方法直接获得。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eab5/4569707/cce5dbb01363/ncomms9101-f1.jpg

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