Cell-Free Multistep Gene Regulatory Cascades Using Eukaryotic ON-Riboswitches Responsive to in Situ Expressed Protein Ligands.

IF 3.7 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS ACS Synthetic Biology Pub Date : 2025-02-24 DOI:10.1021/acssynbio.4c00840
Atsushi Ogawa, Masahiro Fujikawa, Riku Tanimoto, Kiho Matsuno, Riko Uehara, Honami Inoue, Hajime Takahashi
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Abstract

One of the most pressing challenges in cell-free synthetic biology is to assemble well-controlled genetic circuits. However, no complex circuits have been reported in eukaryotic cell-free systems, unlike the case in bacterial ones, despite several unique advantages of the former. We here developed protein-responsive upregulating riboswitches (ON-riboswitches) that function in wheat germ extract to create multistep gene regulatory cascades. Although the initial two types of ON-riboswitches we first designed were less efficient than desired, we improved one of them by incorporating hybridization switches to successfully construct a pair of highly efficient, protein-responsive ON-riboswitches. Both upregulated expression up to 20-fold through self-cleavage by a hammerhead ribozyme (HHR) in response to the corresponding protein ligands expressed in situ. We then combined them with similar types of HHR-based, small-molecule-responsive ON-riboswitches regulating protein ligand expression, to create four kinds of two-step regulatory cascades. Due to the high orthogonality of all the riboswitches used, we also succeeded in regulating two-step cascades concurrently and even in creating three-step cascades. Interestingly, the switching efficiency of each multistep cascade constructed was equivalent to that of the worst step within it. Therefore, more complex cascades with additional steps could be constructed using other efficient and orthogonal, protein-responsive ON-riboswitches with minimal loss of total switching efficiency, although the reaction conditions must be optimized to prevent a reduction of expression efficiencies. Riboswitch-based cascades fashioned through our proposed strategy would aid in the construction of eukaryotic genetic circuits for programmed cell-free systems or artificial cells with functionalities surpassing those of natural cells.

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在无细胞合成生物学中,最紧迫的挑战之一是组装控制良好的遗传回路。然而,尽管真核生物无细胞系统具有一些独特的优势,但与细菌无细胞系统不同,目前还没有关于真核生物无细胞系统中复杂电路的报道。在这里,我们开发了蛋白质反应性上调核糖开关(ON-riboswitches),它在小麦胚芽提取物中发挥作用,创建多步基因调控级联。虽然我们最初设计的两种ON核糖开关的效率低于预期,但我们通过加入杂交开关对其中一种进行了改进,成功构建了一对高效的蛋白反应型ON核糖开关。通过锤头核糖酶(HHR)对原位表达的相应蛋白配体的自清除作用,这两种开关都能使表达上调 20 倍。然后,我们将它们与类似类型的基于 HHR 的小分子反应型 ON-riboswitches 结合起来,形成了四种两步调控级联。由于使用的所有核糖开关都具有高度正交性,我们还成功地同时调控了两步级联,甚至创建了三步级联。有趣的是,所构建的每个多级级联的开关效率与其中最差级联的开关效率相当。因此,尽管必须优化反应条件以防止表达效率降低,但可以使用其他高效、正交、蛋白质响应型核糖核苷开关构建具有额外步骤的更复杂级联,而总的开关效率损失极小。通过我们提出的策略,基于核糖开关的级联将有助于构建真核基因电路,用于无细胞编程系统或具有超越天然细胞功能的人造细胞。
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来源期刊
CiteScore
8.00
自引率
10.60%
发文量
380
审稿时长
6-12 weeks
期刊介绍: The journal is particularly interested in studies on the design and synthesis of new genetic circuits and gene products; computational methods in the design of systems; and integrative applied approaches to understanding disease and metabolism. Topics may include, but are not limited to: Design and optimization of genetic systems Genetic circuit design and their principles for their organization into programs Computational methods to aid the design of genetic systems Experimental methods to quantify genetic parts, circuits, and metabolic fluxes Genetic parts libraries: their creation, analysis, and ontological representation Protein engineering including computational design Metabolic engineering and cellular manufacturing, including biomass conversion Natural product access, engineering, and production Creative and innovative applications of cellular programming Medical applications, tissue engineering, and the programming of therapeutic cells Minimal cell design and construction Genomics and genome replacement strategies Viral engineering Automated and robotic assembly platforms for synthetic biology DNA synthesis methodologies Metagenomics and synthetic metagenomic analysis Bioinformatics applied to gene discovery, chemoinformatics, and pathway construction Gene optimization Methods for genome-scale measurements of transcription and metabolomics Systems biology and methods to integrate multiple data sources in vitro and cell-free synthetic biology and molecular programming Nucleic acid engineering.
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Cell-Free Multistep Gene Regulatory Cascades Using Eukaryotic ON-Riboswitches Responsive to in Situ Expressed Protein Ligands. CnRed: Efficient, Marker-free Genome Engineering of Cupriavidus necator H16 by Adapted Lambda Red Recombineering. Novel Reprogramming of Polyketide Synthase for Valerolactam Production. Issue Publication Information Issue Editorial Masthead
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