一组经过实验验证的、相互正交的引物,用于组合指定遗传成分。

IF 2.6 Q2 BIOCHEMICAL RESEARCH METHODS
Subu K Subramanian, William P Russ, Rama Ranganathan
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引用次数: 2

摘要

设计和合成新的基因和脱氧核糖核酸(DNA)序列是合成生物学的核心技术。目前的高通量基因合成方法使用从定制设计的DNA微阵列芯片中获得的聚合寡核苷酸,并依赖于正交(非相互作用)聚合酶链反应引物,通过扩增特异性地分离组装全长基因所需的精确寡核苷酸子集。因此,大量相互正交的引物的可用性是高通量基因合成的关键试剂。在这里,我们提出了一组166个20核苷酸的引物,这些引物经过实验验证是非相互作用的,能够指定13695个独特的基因。这些引物代表了合成生物学社区的宝贵资源,用于指定可以通过可扩展和模块化架构组装的遗传组件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A set of experimentally validated, mutually orthogonal primers for combinatorially specifying genetic components.

A set of experimentally validated, mutually orthogonal primers for combinatorially specifying genetic components.

A set of experimentally validated, mutually orthogonal primers for combinatorially specifying genetic components.

The design and synthesis of novel genes and deoxyribonucleic acid (DNA) sequences is a central technique in synthetic biology. Current methods of high throughput gene synthesis use pooled oligonucleotides obtained from custom-designed DNA microarray chips, and rely on orthogonal (non-interacting) polymerase chain reaction primers to specifically de-multiplex, by amplification, the precise subset of oligonucleotides necessary to assemble a full length gene. The availability of a large validated set of mutually orthogonal primers is therefore a crucial reagent for high-throughput gene synthesis. Here, we present a set of 166 20-nucleotide primers that are experimentally verified to be non-interacting, capable of specifying 13 695 unique genes. These primers represent a valuable resource to the synthetic biology community for specifying genetic components that can be assembled through a scalable and modular architecture.

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