清脆的
CRISPR干扰
背景(考古学)
RNA干扰
计算生物学
生物
回文
大肠杆菌
合成生物学
核糖核酸
Cas9
反式激活crRNA
电子线路
基因
引导RNA
遗传学
工程类
古生物学
电气工程
作者
Içvara Barbier,Hadiastri Kusumawardhani,Lakshya Chauhan,Pradyumna Harlapur,Mohit Kumar Jolly,Yolanda Schaerli
标识
DOI:10.1021/acssynbio.3c00375
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.
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