Charbgoo Fahimeh, Ishaqat Aman, Chen Junlin, Wiertz Fabian, Kuzmanović Adrian, Bartneck Matthias, Kiessling Fabian, Herrmann Andreas
Institute of Technical and Macromolecular Chemistry, RWTH Aachen University, Aachen, Germany.
DWI - Leibniz Institute for Interactive Materials, Aachen, Germany.
Angew Chem Int Ed Engl. 2025 Jul;64(29):e202421803. doi: 10.1002/anie.202421803. Epub 2025 May 19.
Achieving remote control of biological processes remains a significant challenge in genetics. Although ultrasound has been employed to remotely regulate biological functions by targeting mechanosensitive ion channels, existing systems are constrained by the limited responsiveness of specific channels to specific ultrasound frequencies and their applicability to only a few cell types. Sonogenetics has shown promise for promoter control, thereby regulating gene transcription in eukaryotes. Here, we introduce a new modular toolkit for regulating gene expression using ultrasound-responsive RNA carriers capable of releasing small molecule modulators in response to a broad spectrum of ultrasound frequencies. The cells contain engineered mRNA structures encoding riboswitches or aptazymes, which respond specifically to these small molecule modulators finally controlling downstream protein expression by biocompatible ultrasound. This toolkit is versatile, functioning across various eukaryotic systems-from yeast to mammalian cells-and offers control over gene expression by regulating mRNA translation. We demonstrated that this sonogenetic toolkit robustly modulates gene expression, achieving up to a six-fold downregulation of protein levels in response to ultrasound stimulation. By expanding the application of sonogenetics across eukaryotes, this RNA-based toolkit might provide a promising platform for remotely controlling protein function in specific tissues through on-demand ultrasound activation in the future.
在遗传学领域,实现对生物过程的远程控制仍然是一项重大挑战。尽管超声已被用于通过靶向机械敏感离子通道来远程调节生物功能,但现有系统受到特定通道对特定超声频率的有限响应以及仅适用于少数细胞类型的限制。声遗传学在启动子控制方面显示出前景,从而调节真核生物中的基因转录。在此,我们引入了一种新的模块化工具包,用于使用能够响应广谱超声频率释放小分子调节剂的超声响应性RNA载体来调节基因表达。细胞包含编码核糖开关或适体酶的工程化mRNA结构,它们对这些小分子调节剂产生特异性响应,最终通过生物相容性超声控制下游蛋白质表达。该工具包具有通用性,可在从酵母到哺乳动物细胞的各种真核系统中发挥作用,并通过调节mRNA翻译来控制基因表达。我们证明,这种声遗传学工具包能够强有力地调节基因表达,在超声刺激下实现蛋白质水平高达六倍的下调。通过扩展声遗传学在真核生物中的应用,这种基于RNA的工具包未来可能会为通过按需超声激活在特定组织中远程控制蛋白质功能提供一个有前景的平台。