Banta Amy B, Myers Kevin S, Ward Ryan D, Cuellar Rodrigo A, Place Michael, Freeh Claire C, Bacon Emily E, Peters Jason M
Pharmaceutical Sciences Division, School of Pharmacy, University of Wisconsin-Madison, Madison, WI, USA.
DOE Great Lakes Bioenergy Research Center, University of Wisconsin-Madison, Madison, WI, USA.
bioRxiv. 2024 Mar 4:2024.03.01.582922. doi: 10.1101/2024.03.01.582922.
Targeted, genome-scale gene perturbation screens using Clustered Regularly Interspaced Short Palindromic Repeats interference (CRISPRi) and activation (CRISPRa) have revolutionized eukaryotic genetics, advancing medical, industrial, and basic research. Although CRISPRi knockdowns have been broadly applied in bacteria, options for genome-scale overexpression face key limitations. Here, we develop a facile approach for genome-scale gene overexpression in bacteria we call, "CRISPRtOE" (CRISPR transposition and OverExpression). We create a platform for comprehensive gene targeting using CRISPR-associated transposition (CAST) and show that transposition occurs at a higher frequency in non-transcribed DNA. We then demonstrate that CRISPRtOE can upregulate gene expression in Proteobacteria with medical and industrial relevance by integrating synthetic promoters of varying strength upstream of target genes. Finally, we employ CRISPRtOE screening at the genome-scale in Escherichia coli, recovering known antibiotic targets and genes with unexplored roles in antibiotic function. We envision that CRISPRtOE will be a valuable overexpression tool for antibiotic mode of action, industrial strain optimization, and gene function discovery in bacteria.
使用成簇规律间隔短回文重复序列干扰(CRISPRi)和激活(CRISPRa)进行的靶向基因组规模基因扰动筛选彻底改变了真核生物遗传学,推动了医学、工业和基础研究的发展。尽管CRISPRi敲低技术已在细菌中广泛应用,但基因组规模过表达的方法面临关键限制。在此,我们开发了一种在细菌中进行基因组规模基因过表达的简便方法,我们称之为“CRISPRtOE”(CRISPR转座与过表达)。我们利用与CRISPR相关的转座(CAST)创建了一个全面的基因靶向平台,并表明转座在非转录DNA中发生的频率更高。然后,我们证明CRISPRtOE可以通过在靶基因上游整合不同强度的合成启动子来上调具有医学和工业相关性的变形菌门中的基因表达。最后,我们在大肠杆菌中进行了基因组规模的CRISPRtOE筛选,找到了已知的抗生素靶点以及在抗生素功能中具有未探索作用的基因。我们设想CRISPRtOE将成为研究抗生素作用模式、优化工业菌株以及发现细菌基因功能的有价值的过表达工具。