Potential and Optimization of Mammalian Splice Riboswitches for the Regulation of Exon Skipping-Dependent Gene Expression and Isoform Switching within the ALOX5 Gene.

IF 3.9 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS ACS Synthetic Biology Pub Date : 2025-03-21 Epub Date: 2025-02-26 DOI:10.1021/acssynbio.4c00731
Robin W Bruckhoff, Olga Becker, Dieter Steinhilber, Beatrix Suess
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Abstract

Synthetic riboswitches are attracting increasing interest for a diverse range of applications, including synthetic biology, functional genomics, and prospective therapeutic strategies. This study demonstrates that controlling alternative splicing with synthetic riboswitches represents a promising approach to effectively regulating transgene expression in mammalian cells. However, the function of synthetic riboswitches in the eukaryotic system in controlling gene expression is often limited to certain genes or cell types. So far, strategies to increase the dynamic range of regulation have been focused on adapting and modifying the riboswitch sequence itself without taking into account the context in which the riboswitch was inserted. In the present study, the tetracycline riboswitch was chosen to investigate the effects of the context and insertion site of a cassette exon within the gene to control the expression of an artificial arachidonate 5-lipoxygenase gene (ALOX5) in HEK293 cells. We demonstrate here that the use of riboswitch-controlled cassette exons for the control of gene expression via alternative splicing can be easily transferred to another gene through the process of contextual sequence adaptation. This was achieved through the introduction of gene-specific intronic and exonic sequences with different intron lengths and positions being tested. In contrast, the introduction of nonadapted constructs resulted in an unanticipated functionality outcome of the gene switch. Furthermore, we demonstrate that the combination of two cassette exons into a single gene resulted in a notable enhancement in the dynamic range. Finally, we generated a novel riboswitch-controlled splicing concept that enabled us to switch 5-LO wild-type to expression of an ALOX5 isoform that lacks exon 13 (5-LOΔ13). Taken together, this study demonstrates that synthetic riboswitches that control alternative splicing are a powerful tool to regulate gene expression when applied in combination with gene-specific intronic and exonic sequences.

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哺乳动物剪接开关调控外显子跳脱依赖基因表达和ALOX5基因内异构体切换的潜力和优化
合成核糖开关在合成生物学、功能基因组学和前瞻性治疗策略等领域的应用越来越受到人们的关注。本研究表明,利用合成的核糖开关控制选择性剪接是有效调节哺乳动物细胞中转基因表达的一种很有前途的方法。然而,在真核生物系统中,合成核开关控制基因表达的功能往往局限于某些基因或细胞类型。到目前为止,增加调控动态范围的策略主要集中在适应和修改核糖开关序列本身,而没有考虑到核糖开关插入的环境。在本研究中,选择四环素核素开关来研究基因内盒式外显子的上下文和插入位点对控制人造花生四烯酸5-脂氧合酶基因(ALOX5)在HEK293细胞中的表达的影响。我们在这里证明,使用核糖体开关控制的盒式外显子通过选择性剪接来控制基因表达,可以很容易地通过上下文序列适应过程转移到另一个基因上。这是通过引入具有不同内含子长度和位置的基因特异性内含子和外显子序列来实现的。相反,引入非适应性结构会导致基因开关产生意想不到的功能结果。此外,我们证明了将两个盒式外显子组合成一个基因导致动态范围的显着增强。最后,我们生成了一个新的核糖开关控制剪接概念,使我们能够将5-LO野生型转换为缺乏外显子13的ALOX5异构体的表达(5-LOΔ13)。综上所述,本研究表明,当与基因特异性内含子和外显子序列结合使用时,控制选择性剪接的合成核糖开关是调节基因表达的有力工具。
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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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