CRISPRi-Linked Multimodule Negative Feedback Loops to Address Winner-Take-All Resource Competition

IF 3.9 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Sadikshya Rijal, Kylie Standage-Beier, Rong Zhang, Austin Stone, Abdelrahman Youssef, Xiao Wang and Xiao-Jun Tian*, 
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Abstract

Cellular resource limitations create unintended interactions among synthetic gene circuit modules, compromising circuit modularity. This challenge is particularly pronounced in circuits with positive feedback, where uneven resource allocation can lead to Winner-Takes-All (WTA) behavior, favoring one module at the expense of others. In this study, we experimentally implemented a Negatively Competitive Regulatory (NCR) controller using CRISPR interference (CRISPRi) and evaluated its effectiveness in mitigating WTA behavior in two gene circuits: dual self-activation and cascading bistable switch. We chromosomally integrated a tunable dCas9 gene and designed module-specific gRNAs, with each module encoding its own gRNA to self-repress via competition for limited dCas9. This configuration introduces strong negative feedback to the more active module while reallocating resources to the less active one, promoting balanced module activation. Compared to the control group lacking dCas9-mediated repression, the NCR controller significantly increased module coactivation and suppressed WTA behavior. Our quantitative results demonstrate that NCR provides an effective strategy for regulating resource competition and improving the modularity of synthetic gene circuits.

Abstract Image

与crispr相关的多模块负反馈循环解决赢者通吃的资源竞争
细胞资源的限制在合成基因电路模块之间产生了意想不到的相互作用,损害了电路的模块化。这一挑战在具有正反馈的电路中尤其明显,其中不均衡的资源分配可能导致赢家通吃(WTA)行为,即以牺牲其他模块为代价来支持一个模块。在这项研究中,我们利用CRISPR干扰(CRISPRi)实验实现了一个负竞争调控(NCR)控制器,并评估了其在两个基因回路(双自激活和级联双稳态开关)中减轻WTA行为的有效性。我们在染色体上整合了一个可调节的dCas9基因,并设计了模块特异性gRNA,每个模块编码自己的gRNA,通过竞争有限的dCas9进行自我抑制。此配置向活动较多的模块引入了强烈的负反馈,同时将资源重新分配给活动较少的模块,从而促进均衡的模块激活。与缺乏dcas9介导抑制的对照组相比,NCR控制器显著增加了模块共激活并抑制了WTA行为。我们的定量结果表明,NCR为调节资源竞争和提高合成基因电路的模块化提供了有效的策略。
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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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