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合成TALE激活启动子文库:方法与应用

Libraries of Synthetic TALE-Activated Promoters: Methods and Applications.

作者信息

Schreiber T, Tissier A

机构信息

Leibniz Institute of Plant Biochemistry, Halle (Saale), Germany.

Leibniz Institute of Plant Biochemistry, Halle (Saale), Germany.

出版信息

Methods Enzymol. 2016;576:361-78. doi: 10.1016/bs.mie.2016.03.004. Epub 2016 Apr 4.

Abstract

The discovery of proteins with programmable DNA-binding specificities triggered a whole array of applications in synthetic biology, including genome editing, regulation of transcription, and epigenetic modifications. Among those, transcription activator-like effectors (TALEs) due to their natural function as transcription regulators, are especially well-suited for the development of orthogonal systems for the control of gene expression. We describe here the construction and testing of libraries of synthetic TALE-activated promoters which are under the control of a single TALE with a given DNA-binding specificity. These libraries consist of a fixed DNA-binding element for the TALE, a TATA box, and variable sequences of 19 bases upstream and 43 bases downstream of the DNA-binding element. These libraries were cloned using a Golden Gate cloning strategy making them usable as standard parts in a modular cloning system. The broad range of promoter activities detected and the versatility of these promoter libraries make them valuable tools for applications in the fine-tuning of expression in metabolic engineering projects or in the design and implementation of regulatory circuits.

摘要

具有可编程DNA结合特异性的蛋白质的发现引发了合成生物学中的一系列应用,包括基因组编辑、转录调控和表观遗传修饰。其中,转录激活样效应因子(TALEs)由于其作为转录调节因子的天然功能,特别适合用于开发用于控制基因表达的正交系统。我们在此描述了合成TALE激活启动子文库的构建和测试,这些启动子文库受具有给定DNA结合特异性的单个TALE的控制。这些文库由TALE的固定DNA结合元件、TATA框以及DNA结合元件上游19个碱基和下游43个碱基的可变序列组成。这些文库使用金门克隆策略进行克隆,使其可作为模块化克隆系统中的标准部件使用。检测到的广泛的启动子活性以及这些启动子文库的多功能性使其成为代谢工程项目中表达微调或调控电路设计与实施应用中的有价值工具。

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