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Artificial Zinc Finger DNA Binding Domains: Versatile Tools for Genome Engineering and Modulation of Gene Expression

机译:人工锌指DNA结合域:基因组工程和基因表达调节的多功能工具。

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摘要

Genome editing and alteration of gene expression by synthetic DNA binding activities gained a lot of momentum over the last decade. This is due to the development of new DNA binding molecules with enhanced binding specificity. The most commonly used DNA binding modules are zinc fingers (ZFs), TALE-domains, and the RNA component of the CRISPR/Cas9 system. These binding modules are fused or linked to either nucleases that cut the DNA and induce DNA repair processes, or to protein domains that activate or repress transcription of genes close to the targeted site in the genome. This review focuses on the structure, design, and applications of ZF DNA binding domains (ZFDBDs). ZFDBDs are relatively small and have been shown to penetrate the cell membrane without additional tags suggesting that they could be delivered to cells without a DNA or RNA intermediate. Advanced algorithms that are based on extensive knowledge of the mode of ZF/DNA interactions are used to design the amino acid composition of ZFDBDs so that they bind to unique sites in the genome. Off-target binding has been a concern for all synthetic DNA binding molecules. Thus, increasing the specificity and affinity of ZFDBDs will have a significant impact on their use in analytical or therapeutic settings.
机译:在过去的十年中,通过合成DNA结合活性进行基因组编辑和基因表达改变的势头很大。这是由于开发了具有增强的结合特异性的新的DNA结合分子。最常用的DNA结合模块是锌指(ZF),TALE域和CRISPR / Cas9系统的RNA组件。这些结合模块与切割DNA并诱导DNA修复过程的核酸酶融合,或与激活或抑制接近基因组目标位点的基因转录的蛋白质域融合或连接。这篇评论集中在ZF DNA结合域(ZFDBDs)的结构,设计和应用。 ZFDBD相对较小,已显示出穿透细胞膜而没有其他标签,这表明ZFDBD可以在没有DNA或RNA中间体的情况下被递送至细胞。基于对ZF / DNA相互作用模式的广泛了解的先进算法可用于设计ZFDBD的氨基酸组成,使其与基因组中的独特位点结合。脱靶结合一直是所有合成DNA结合分子的关注点。因此,增加ZFDBD的特异性和亲和力将对其在分析或治疗环境中的使用产生重大影响。

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