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利用 RNA 折纸支架在酿酒酵母中进行 dCas9 介导的转录调控。

Utilizing RNA origami scaffolds in Saccharomyces cerevisiae for dCas9-mediated transcriptional control.

机构信息

Interdisciplinary Nanoscience Center, Aarhus University, 8000 Aarhus C, Denmark.

Department of Molecular Biology and Genetics, Aarhus University, 8000 Aarhus C, Denmark.

出版信息

Nucleic Acids Res. 2022 Jul 8;50(12):7176-7187. doi: 10.1093/nar/gkac470.

Abstract

Designer RNA scaffolds constitute a promising tool for synthetic biology, as they can be genetically expressed to perform specific functions in vivo such as scaffolding enzymatic cascades and regulating gene expression through CRISPR-dCas9 applications. RNA origami is a recently developed RNA design approach that allows construction of large RNA nanostructures that can position aptamer motifs to spatially organize other molecules, including proteins. However, it is still not fully understood how positioning multiple aptamers on a scaffold and the orientation of a scaffold affects functional properties. Here, we investigate fusions of single-guide RNAs and RNA origami scaffolds (termed sgRNAO) capable of recruiting activating domains for control of gene expression in yeast. Using MS2 and PP7 as orthogonal protein-binding aptamers, we observe a gradual increase in transcriptional activation for up to four aptamers. We demonstrate that different aptamer positions on a scaffold and scaffold orientation affect transcriptional activation. Finally, sgRNAOs are used to regulate expression of enzymes of the violacein biosynthesis pathway to control metabolic flux. The integration of RNA origami nanostructures at promoter sites achieved here, can in the future be expanded by the addition of functional motifs such as riboswitches, ribozymes and sensor elements to allow for complex gene regulation.

摘要

设计 RNA 支架是合成生物学的一种很有前途的工具,因为它们可以通过基因表达在体内执行特定的功能,例如支架酶级联和通过 CRISPR-dCas9 应用调节基因表达。RNA 折纸术是一种最近开发的 RNA 设计方法,允许构建可以定位适体基序的大型 RNA 纳米结构,从而对其他分子(包括蛋白质)进行空间组织。然而,目前尚不完全清楚如何在支架上定位多个适体以及支架的方向如何影响功能特性。在这里,我们研究了能够招募激活域以控制酵母中基因表达的单指导 RNA 和 RNA 折纸支架(称为 sgRNAO)的融合。我们使用 MS2 和 PP7 作为正交蛋白结合适体,观察到多达四个适体的转录激活逐渐增加。我们证明了支架上不同的适体位置和支架方向会影响转录激活。最后,sgRNAO 用于调节类病毒生物合成途径中酶的表达以控制代谢通量。在这里实现的 RNA 折纸纳米结构的整合,可以通过添加功能基序(如核糖开关、核酶和传感器元件)来扩展,从而实现复杂的基因调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/466b/9262615/8c27aa5b212f/gkac470fig1.jpg

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