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Multistable and dynamic CRISPRi-based synthetic circuits in E coli

biorxiv. 2019; 
Javier Santos-Moreno, Yolanda Schaerli
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Gene Synthesis Genes encoding sfGFP, mKO2, mKate2, Csy4 and dCas9 were obtained as previously described29. mCherry and mCitrine were amplified from plasmids (pLacI(r)-mCherry(ASV) and pCI-Citrine-(ASV)) kindly provided by Sebastian Maerkl36. dBroccoli was amplified from plasmid pET28c-F30-2xdBroccoli, which was a gift from Samie Jaffrey (Addgene plasmid #66843). Cerulean38 was purchased as an E. coli codon-optimized gBlock from IDT, and LuxR (BBa_C0062) was also codon-optimized and synthesized by GenScript Get A Quote

摘要

Gene expression control based on CRISPRi (clustered regularly interspaced short palindromic repeats interference) has emerged as a powerful tool for creating synthetic gene circuits, both in prokaryotes and in eukaryotes; yet, its lack of cooperativity has been pointed out as a potential obstacle for dynamic or multistable circuit construction, raising the question of whether CRISPRi is widely applicable for synthetic circuit design. Here we use CRISPRi to build prominent synthetic gene circuits that accurately govern temporal and spatial gene expression in Escherichia coli. We report the first-ever CRSPRi oscillator (“CRISPRlator”), bistable network and stripe pattern-forming incoherent feed-forward loop ... More

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