Department of Biomedical Engineering, Chung-Ang University, Seoul 06974, Republic of Korea.
ACS Synth Biol. 2024 Oct 18;13(10):3256-3267. doi: 10.1021/acssynbio.4c00323. Epub 2024 Sep 18.
Synthetic sRNAs show promise as tools for targeted and programmable gene expression manipulation. However, the design of high-efficiency synthetic sRNAs is a challenging task that necessitates careful consideration of multiple factors. Therefore, this study aims to investigate rational design strategies that significantly and robustly enhance the efficiency of synthetic sRNAs. This is achieved by optimizing the following parameters: the sRNA scaffold, mRNA binding affinity, Hfq protein expression level, and mRNA secondary structure. By utilizing optimized synthetic sRNAs within a positive feedback circuit, we effectively addressed the issue of gene expression leakage─an enduring challenge in synthetic biology that undermines the reliability of genetic circuits in bacteria. Our designed synthetic sRNAs successfully prevented gene expression leakage, thus averting unintended circuit activation caused by initial expression noise, even in the absence of signal molecules. This result shows that high-efficiency synthetic sRNAs not only enable precise gene knockdown for metabolic engineering but also ensure the robust performance of synthetic circuits. The strategies developed here hold significant promise for broad applications across diverse biotechnological fields, establishing synthetic sRNAs as pivotal tools in advancing synthetic biology and gene regulation.
合成 sRNA 有望成为靶向和可编程基因表达操纵的工具。然而,设计高效的合成 sRNA 是一项具有挑战性的任务,需要仔细考虑多个因素。因此,本研究旨在探讨显著增强合成 sRNA 效率的合理设计策略。这是通过优化以下参数实现的:sRNA 支架、mRNA 结合亲和力、Hfq 蛋白表达水平和 mRNA 二级结构。通过在正反馈回路中使用优化的合成 sRNA,我们有效地解决了基因表达泄漏的问题——这是合成生物学中长期存在的一个挑战,会破坏细菌中遗传回路的可靠性。我们设计的合成 sRNA 成功地防止了基因表达泄漏,从而避免了由于初始表达噪声引起的意外电路激活,即使没有信号分子也是如此。这一结果表明,高效的合成 sRNA 不仅可以实现代谢工程中精确的基因敲低,还可以确保合成电路的稳健性能。这里开发的策略在广泛的生物技术领域具有重要的应用前景,使合成 sRNA 成为推进合成生物学和基因调控的关键工具。