School of Biological Sciences, University of Edinburgh, Edinburgh, EH9 3FF, UK.
Centre for Synthetic and Systems Biology, University of Edinburgh, Edinburgh, EH9 3FF, UK.
Nat Commun. 2019 Aug 26;10(1):3693. doi: 10.1038/s41467-019-11479-0.
Transcriptional regulation by nuclease-deficient CRISPR/Cas is a popular and valuable tool for routine control of gene expression. CRISPR interference in bacteria can be reliably achieved with high efficiencies. Yet, options for CRISPR activation (CRISPRa) remained limited in flexibility and activity because they relied on σ promoters. Here we report a eukaryote-like bacterial CRISPRa system based on σ-dependent promoters, which supports long distance, and hence multi-input regulation with high dynamic ranges. Our CRISPRa device can activate σ-dependent promoters with biotechnology relevance in non-model bacteria. It also supports orthogonal gene regulation on multiple levels. Combining our CRISPRa with dxCas9 further expands flexibility in DNA targeting, and boosts dynamic ranges into regimes that enable construction of cascaded CRISPRa circuits. Application-wise, we construct a reusable scanning platform for readily optimizing metabolic pathways without library reconstructions. This eukaryote-like CRISPRa system is therefore a powerful and versatile synthetic biology tool for diverse research and industrial applications.
无核酸酶活性的 CRISPR/Cas 的转录调控是一种常用于常规基因表达控制的流行且有价值的工具。CRISPR 干扰在细菌中可以可靠地实现高效率。然而,CRISPR 激活(CRISPRa)的选择在灵活性和活性方面仍然受到限制,因为它们依赖于σ启动子。在这里,我们报告了一种基于σ依赖性启动子的真核细菌 CRISPRa 系统,它支持远距离,因此具有高动态范围的多输入调节。我们的 CRISPRa 设备可以激活具有生物技术相关性的非模型细菌中的σ依赖性启动子。它还支持多个层次的正交基因调控。将我们的 CRISPRa 与 dxCas9 结合使用,进一步扩展了 DNA 靶向的灵活性,并将动态范围提高到可以构建级联 CRISPRa 电路的水平。在应用方面,我们构建了一个可重复使用的扫描平台,可在无需文库重建的情况下轻松优化代谢途径。因此,这种真核细菌 CRISPRa 系统是一种强大而通用的合成生物学工具,适用于各种研究和工业应用。