Rational design of inducible CRISPR guide RNAs for de novo assembly of transcriptional programs

Quentin R. V. Ferry, Radostina Lyutova and Tudor A. Fulga ()
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Quentin R. V. Ferry: Weatherall Institute of Molecular Medicine, University of Oxford
Radostina Lyutova: Weatherall Institute of Molecular Medicine, University of Oxford
Tudor A. Fulga: Weatherall Institute of Molecular Medicine, University of Oxford

Nature Communications, 2017, vol. 8, issue 1, 1-10

Abstract: Abstract CRISPR-based transcription regulators (CRISPR-TRs) have transformed the current synthetic biology landscape by allowing specific activation or repression of any target gene. Here we report a modular and versatile framework enabling rapid implementation of inducible CRISPR-TRs in mammalian cells. This strategy relies on the design of a spacer-blocking hairpin (SBH) structure at the 5′ end of the single guide RNA (sgRNA), which abrogates the function of CRISPR-transcriptional activators. By replacing the SBH loop with ligand-controlled RNA-cleaving units, we demonstrate conditional activation of quiescent sgRNAs programmed to respond to genetically encoded or externally delivered triggers. We use this system to couple multiple synthetic and endogenous target genes with specific inducers, and assemble gene regulatory modules demonstrating parallel and orthogonal transcriptional programs. We anticipate that this ‘plug and play’ approach will be a valuable addition to the synthetic biology toolkit, facilitating the understanding of natural gene circuits and the design of cell-based therapeutic strategies.

Date: 2017
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DOI: 10.1038/ncomms14633

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