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用于酿酒酵母基因表达直系调控的植物源转录因子

Plant-Derived Transcription Factors for Orthologous Regulation of Gene Expression in the Yeast Saccharomyces cerevisiae.

作者信息

Naseri Gita, Balazadeh Salma, Machens Fabian, Kamranfar Iman, Messerschmidt Katrin, Mueller-Roeber Bernd

机构信息

Plant Signalling Group, Max-Planck Institute of Molecular Plant Physiology , Am Mühlenberg 1, Potsdam, 14476, Germany.

出版信息

ACS Synth Biol. 2017 Sep 15;6(9):1742-1756. doi: 10.1021/acssynbio.7b00094. Epub 2017 Jun 9.

DOI:10.1021/acssynbio.7b00094
PMID:28531348
Abstract

Control of gene expression by transcription factors (TFs) is central in many synthetic biology projects for which a tailored expression of one or multiple genes is often needed. As TFs from evolutionary distant organisms are unlikely to affect gene expression in a host of choice, they represent excellent candidates for establishing orthogonal control systems. To establish orthogonal regulators for use in yeast (Saccharomyces cerevisiae), we chose TFs from the plant Arabidopsis thaliana. We established a library of 106 different combinations of chromosomally integrated TFs, activation domains (yeast GAL4 AD, herpes simplex virus VP64, and plant EDLL) and synthetic promoters harboring cognate cis-regulatory motifs driving a yEGFP reporter. Transcriptional output of the different driver/reporter combinations varied over a wide spectrum, with EDLL being a considerably stronger transcription activation domain in yeast than the GAL4 activation domain, in particular when fused to Arabidopsis NAC TFs. Notably, the strength of several NAC-EDLL fusions exceeded that of the strong yeast TDH3 promoter by 6- to 10-fold. We furthermore show that plant TFs can be used to build regulatory systems encoded by centromeric or episomal plasmids. Our library of TF-DNA binding site combinations offers an excellent tool for diverse synthetic biology applications in yeast.

摘要

转录因子(TFs)对基因表达的调控在许多合成生物学项目中至关重要,这些项目通常需要对一个或多个基因进行定制表达。由于来自进化距离较远生物体的转录因子不太可能影响所选宿主中的基因表达,它们是建立正交控制系统的优秀候选者。为了建立用于酵母(酿酒酵母)的正交调控因子,我们选择了来自植物拟南芥的转录因子。我们建立了一个包含106种不同组合的文库,这些组合包括染色体整合的转录因子、激活结构域(酵母GAL4 AD、单纯疱疹病毒VP64和植物EDLL)以及带有驱动yEGFP报告基因的同源顺式调控基序的合成启动子。不同驱动/报告基因组合的转录输出差异很大,EDLL在酵母中是比GAL4激活结构域更强的转录激活结构域,特别是当与拟南芥NAC转录因子融合时。值得注意的是,几种NAC-EDLL融合蛋白的强度比强大的酵母TDH3启动子高出6至10倍。我们还表明,植物转录因子可用于构建由着丝粒或附加体质粒编码的调控系统。我们的转录因子-DNA结合位点组合文库为酵母中的各种合成生物学应用提供了一个优秀的工具。

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