Wu Han, Wang Fenglin, Jiang Jian-Hui
State Key Laboratory of Chemo/Bio-Sensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, 410082, P. R. China.
Chembiochem. 2021 Jun 2;22(11):1894-1900. doi: 10.1002/cbic.202000723. Epub 2021 Mar 3.
The clustered, regularly interspaced short palindromic repeats-associated protein 9 endonuclease (CRISPR-Cas9) and the nuclease-deactivated Cas9 (dCas9) systems have revolutionized our ability to precisely engineer and regulate genomes. Inducible CRISPR-dCas9-based transcriptional systems have been rapidly developed to conditionally control genetic manipulation. Current strategies mainly focus on conditional control of gRNA function and dCas9 protein using exogenous and endogenous triggers, including external light, small molecules, synthetic and intracellular oligonucleotides. These strategies have established novel platforms for the spatiotemporal regulation of genome activation and repression, epigenome editing, and so on. Herein, we summarize the recent progress in conditionally controlling CRISPR-dCas9 transcriptional systems through gRNA modulation and dCas9 protein engineering.
成簇规律间隔短回文重复序列相关蛋白9核酸酶(CRISPR-Cas9)和核酸酶失活的Cas9(dCas9)系统彻底改变了我们精确改造和调控基因组的能力。基于可诱导CRISPR-dCas9的转录系统已迅速发展,用于条件性控制基因操作。目前的策略主要集中于利用外源性和内源性触发因素(包括外部光照、小分子、合成及细胞内寡核苷酸)对gRNA功能和dCas9蛋白进行条件性控制。这些策略为基因组激活与抑制、表观基因组编辑等的时空调控建立了新的平台。在此,我们总结了通过gRNA调控和dCas9蛋白工程对CRISPR-dCas9转录系统进行条件性控制的最新进展。