Synthetic Gene Circuits Combining CRISPR Interference and CRISPR Activation in E. coli: Importance of Equal Guide RNA Binding Affinities to Avoid Context-Dependent Effects

被引:8
作者
Barbier, Icvara [1 ]
Kusumawardhani, Hadiastri [1 ]
Chauhan, Lakshya [1 ,2 ]
Harlapur, Pradyumna Vinod [2 ]
Kumar, Jolly Mohit [2 ]
Schaerli, Yolanda [1 ]
机构
[1] Univ Lausanne, Dept Fundamental Microbiol, CH-1015 Lausanne, Switzerland
[2] Indian Inst Sci, Dept Bioengn, Bengaluru 560012, India
基金
瑞士国家科学基金会;
关键词
bacterial synthetic biology; synthetic gene circuits; CRISPR interference; CRISPR activation; resourcecompetition; dCas9; TRANSCRIPTIONAL ACTIVATION; BIOLOGY; REPRESSION; SYSTEMS; BUILD;
D O I
10.1021/acssynbio.3c00375
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Gene expression control based on clustered regularly interspaced short palindromic repeats (CRISPR) has emerged as a powerful approach for constructing synthetic gene circuits. While the use of CRISPR interference (CRISPRi) is already well-established in prokaryotic circuits, CRISPR activation (CRISPRa) is less mature, and a combination of the two in the same circuits is only just emerging. Here, we report that combining CRISPRi with SoxS-based CRISPRa in Escherichia coli can lead to context-dependent effects due to different affinities in the formation of CRISPRa and CRISPRi complexes, resulting in loss of predictable behavior. We show that this effect can be avoided by using the same scaffold guide RNA structure for both complexes.
引用
收藏
页码:3064 / 3071
页数:8
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