Programmable CRISPR‐Cas transcriptional activation in bacteria
Hsing‐I Ho, Jennifer R Fang, Jacky Cheung, Harris H Wang

TL;DR
A new CRISPR-based system allows precise control of gene expression in bacteria, enabling both activation and repression of genes.
Contribution
The development of dCas9-AsiA, a novel CRISPR activator that enables strong and programmable gene regulation in bacteria.
Findings
dCas9-AsiA can activate gene expression by over 200-fold across diverse promoters in E. coli.
The system allows simultaneous activation and repression of bacterial regulons.
dCas9-AsiA can be applied to other bacteria of clinical and industrial importance.
Abstract
Programmable gene activation enables fine‐tuned regulation of endogenous and synthetic gene circuits to control cellular behavior. While CRISPR‐Cas‐mediated gene activation has been extensively developed for eukaryotic systems, similar strategies have been difficult to implement in bacteria. Here, we present a generalizable platform for screening and selection of functional bacterial CRISPR‐Cas transcription activators. Using this platform, we identified a novel CRISPR activator, dCas9‐AsiA, that could activate gene expression by more than 200‐fold across genomic and plasmid targets with diverse promoters after directed evolution. The evolved dCas9‐AsiA can simultaneously mediate activation and repression of bacterial regulons in E. coli. We further identified hundreds of promoters with varying basal expression that could be induced by dCas9‐AsiA, which provides a rich resource of…
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Taxonomy
TopicsCRISPR and Genetic Engineering · Bacterial Genetics and Biotechnology
