通用环路组装:开放、高效和跨领域的 DNA 制造。

IF 2.6 Q2 BIOCHEMICAL RESEARCH METHODS Synthetic biology (Oxford, England) Pub Date : 2020-01-01 Epub Date: 2020-02-05 DOI:10.1093/synbio/ysaa001
Bernardo Pollak, Tamara Matute, Isaac Nuñez, Ariel Cerda, Constanza Lopez, Valentina Vargas, Anton Kan, Vincent Bielinski, Peter von Dassow, Chris L Dupont, Fernán Federici
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引用次数: 0

摘要

标准化的 IIS 型 DNA 组装方法正成为生物工程和研究的关键。由于 "通用语法 "的提出,DNA 文库之间的互操作性更强,因此这些方法正变得越来越普遍,也越来越容易获得。目前,最初在宿主特异性载体中实现的基于金门(GG)的组装系统,正在实现与多种生物的兼容。我们最近为植物开发了基于 GG 的 Loop 组装系统,该系统使用一个小型文库和一种直观的策略来分层构建大型 DNA 构建体(大于 30 kb)。在这里,我们将介绍 "通用 Loop"(uLoop)组装,这是一种基于 Loop 组装的系统,可用于任何生物体。这种设计允许使用数量较少的质粒(奇数载体和偶数载体各四组),在交替步骤中重复使用。在目标生物体内进行转化/维护所需的元件也作为标准化部件进行组装,从而实现了宿主特异性质粒的定制。将环路组装逻辑与宿主特异性传播元件解耦,可实现通用 DNA 组装,无论最终宿主是谁,都能保持高效率。作为概念验证,我们展示了硅藻、酵母、植物和细菌的多基因表达载体工程。这些资源可通过 OpenMTA 无限制共享和开放访问。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Universal loop assembly: open, efficient and cross-kingdom DNA fabrication.

Standardized type IIS DNA assembly methods are becoming essential for biological engineering and research. These methods are becoming widespread and more accessible due to the proposition of a 'common syntax' that enables higher interoperability between DNA libraries. Currently, Golden Gate (GG)-based assembly systems, originally implemented in host-specific vectors, are being made compatible with multiple organisms. We have recently developed the GG-based Loop assembly system for plants, which uses a small library and an intuitive strategy for hierarchical fabrication of large DNA constructs (>30 kb). Here, we describe 'universal Loop' (uLoop) assembly, a system based on Loop assembly for use in potentially any organism of choice. This design permits the use of a compact number of plasmids (two sets of four odd and even vectors), which are utilized repeatedly in alternating steps. The elements required for transformation/maintenance in target organisms are also assembled as standardized parts, enabling customization of host-specific plasmids. Decoupling of the Loop assembly logic from the host-specific propagation elements enables universal DNA assembly that retains high efficiency regardless of the final host. As a proof-of-concept, we show the engineering of multigene expression vectors in diatoms, yeast, plants and bacteria. These resources are available through the OpenMTA for unrestricted sharing and open access.

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