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FungalBraid:一种基于 GoldenBraid 的模块化克隆平台,用于组装和交换定制真菌合成生物学的 DNA 元件。

FungalBraid: A GoldenBraid-based modular cloning platform for the assembly and exchange of DNA elements tailored to fungal synthetic biology.

机构信息

Department of Food Biotechnology, Instituto de Agroquímica y Tecnología de Alimentos (IATA), Consejo Superior de Investigaciones Científicas (CSIC), Avda Agustín Escardino 7, 46980 Paterna, Valencia, Spain.

Instituto de Biología Molecular y Celular de Plantas (IBMCP), Universitat Politècnica de València-Consejo Superior de Investigaciones Científicas (CSIC) 46022 Valencia, Spain.

出版信息

Fungal Genet Biol. 2018 Jul;116:51-61. doi: 10.1016/j.fgb.2018.04.010. Epub 2018 Apr 20.

Abstract

Current challenges in the study and biotechnological exploitation of filamentous fungi are the optimization of DNA cloning and fungal genetic transformation beyond model fungi, the open exchange of ready-to-use and standardized genetic elements among the research community, and the availability of universal synthetic biology tools and rules. The GoldenBraid (GB) cloning framework is a Golden Gate-based DNA cloning system developed for plant synthetic biology through Agrobacterium tumefaciens-mediated genetic transformation (ATMT). In this study, we develop reagents for the adaptation of GB version 3.0 from plants to filamentous fungi through: (i) the expansion of the GB toolbox with the domestication of fungal-specific genetic elements; (ii) the design of fungal-specific GB structures; and (iii) the ATMT and gene disruption of the plant pathogen Penicillium digitatum as a proof of concept. Genetic elements domesticated into the GB entry vector pUPD2 include promoters, positive and negative selection markers and terminators. Interestingly, some GB elements can be directly exchanged between plants and fungi, as demonstrated with the marker hph for Hyg or the fluorescent protein reporter YFP. The iterative modular assembly of elements generates an endless number of diverse transcriptional units and other higher order combinations in the pDGB3α/pDGB3Ω destination vectors. Furthermore, the original plant GB syntax was adapted here to incorporate specific GB structures for gene disruption through homologous recombination and dual selection. We therefore have successfully adapted the GB technology for the ATMT of fungi. We propose the name of FungalBraid (FB) for this new branch of the GB technology that provides open, exchangeable and collaborative resources to the fungal research community.

摘要

当前,丝状真菌研究和生物技术开发所面临的挑战包括:超越模式真菌,优化 DNA 克隆和真菌遗传转化;在研究群体中公开交流即用型和标准化遗传元件;以及提供通用的合成生物学工具和规则。GoldenBraid(GB)克隆框架是一个基于 Golden Gate 的 DNA 克隆系统,最初是为植物合成生物学开发的,通过根癌农杆菌介导的遗传转化(ATMT)实现。在这项研究中,我们通过以下方式开发了将 GB 版本 3.0 从植物适应到丝状真菌的试剂:(i)通过驯化真菌特异性遗传元件扩展 GB 工具包;(ii)设计真菌特异性 GB 结构;(iii)通过 ATMT 和基因敲除植物病原菌Penicillium digitatum 进行概念验证。驯化到 GB 入口载体 pUPD2 的遗传元件包括启动子、正负选择标记和终止子。有趣的是,一些 GB 元件可以在植物和真菌之间直接交换,这可以通过 Hyg 标记 hph 或荧光蛋白报告基因 YFP 证明。通过迭代模块化组装元件,在 pDGB3α/pDGB3Ω 目的载体中生成无数种不同的转录单元和其他更高阶的组合。此外,这里还对原始的植物 GB 语法进行了改编,以纳入通过同源重组和双重选择进行基因敲除的特定 GB 结构。因此,我们成功地将 GB 技术适应于真菌的 ATMT。我们将这个 GB 技术的新分支命名为 FungalBraid(FB),为真菌研究群体提供了开放、可交换和协作的资源。

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