Abstract
The investigation and manipulation of cellular processes with subcellular resolution requires non-invasive tools with spatiotemporal precision and reversibility. Building on the interaction of the photoreceptor PAL with an RNA aptamer, we describe a variation of the CRISPR/dCAS9 system for light-controlled activation of gene expression. This platform significantly reduces the coding space required for genetic manipulation and provides a strong on-switch with almost no residual activity in the dark. It adds to the current set of modular building blocks for synthetic biological circuit design and is broadly applicable.
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Renzl, C., Kakoti, A., & Mayer, G. (2020). Aptamer-Mediated Reversible Transactivation of Gene Expression by Light. Angewandte Chemie - International Edition, 59(50), 22414–22418. https://doi.org/10.1002/anie.202009240
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