He Miao, Zhou Xiang, Li Zhigang, Yin Xue, Han Wenjie, Zhou Junxiang, Sun Xiaoyun, Liu Xiaoyu, Yao Dongbao, Liang Haojun
School of Chemistry and Materials Science, Department of Polymer Science and Engineering, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials), University of Science and Technology of China, Hefei, Anhui 230026, China.
J Am Chem Soc. 2022 Jul 20;144(28):12690-12697. doi: 10.1021/jacs.2c02271. Epub 2022 Jul 6.
Multi-module dCas9 engineering systems have been developed for controllable transcriptional manipulation such as chemical- or light-induced systems. However, there is still a need for a separate module that can be used for internal control over the CRISPR-dCas9 system. Here, we describe a multi-module CRISPR-dCas9 system in which a separate structured RNA was applied as a programmable component that could control dCas9-based gene regulation and achieved a higher activation efficiency than dCas9-VPR that is traditionally used. By introducing a microRNA sensor, we generated a dCas9-based transcriptional regulation platform that responded to endogenous microRNAs and allowed controllable activation of endogenous genes. Moreover, we applied the platform to selectively identify HCT116 cells in a cell mixture. This work provides a flexible platform for efficient and controllable gene regulation based on CRISPR-dCas9.
多模块dCas9工程系统已被开发用于可控的转录操作,如化学或光诱导系统。然而,仍然需要一个可用于对CRISPR-dCas9系统进行内部控制的单独模块。在此,我们描述了一种多模块CRISPR-dCas9系统,其中一个单独的结构化RNA被用作可编程组件,它可以控制基于dCas9的基因调控,并且比传统使用的dCas9-VPR具有更高的激活效率。通过引入一个微小RNA传感器,我们构建了一个基于dCas9的转录调控平台,该平台对内源性微小RNA作出反应,并允许对内源基因进行可控激活。此外,我们应用该平台在细胞混合物中选择性识别HCT116细胞。这项工作为基于CRISPR-dCas9的高效且可控的基因调控提供了一个灵活的平台。