Metabolite-responsive scaffold RNAs for dynamic CRISPR transcriptional regulation
CRISPR activation is a powerful tool to upregulate a vast array of genes in many different contexts. However, there are few dynamic CRISPR transcriptional programs, which limit its usage in the creation of living biosensors, self-regulating microbial factories, or conditional therapeutics. Here, we address this limitation by embedding a molecular switch directly into a guide RNA to create a combined sensor-actuator called a metabolite-responsive scaffold RNA (MR-scRNA). We demonstrate the regulatory potential for MR-scRNAs by conditionally activating genes in three different kingdoms of life. We create MR-scRNAs responsive to two distinct metabolites, theophylline and tryptophan, by swapping the molecular switch used. MR-scRNAs respond quickly in a dose-dependent manner specifically to their target metabolite and enhance biochemical production when used as a dynamic regulator of pathway enzyme expression. The broad functionality and ease of design of the MR-scRNAs offer a promising tool for dynamic cellular regulation.
Authors
- Blake A. Richards (ORCID: https://orcid.org/0000-0001-9662-2151)
- Mark Blenner (ORCID: https://orcid.org/0000-0001-9274-3749)
- Helena Hansen
- Wilfred Chen (ORCID: https://orcid.org/0000-0002-6386-6958)
- Antonio G Goncalves
- Ayushi Agrawal (ORCID: https://orcid.org/0000-0001-7081-3304)
- Anthony M Stohr (ORCID: https://orcid.org/0000-0002-2388-1723)
- Hayeon Park
Institutions
- University of Delaware (US)
Publication Details
- Journal
- Nucleic Acids Research
- Published
- 2025-11-13
- DOI
- https://doi.org/10.1093/nar/gkaf1290
- Primary Topic
- CRISPR and Genetic Engineering
- Type
- article
- Field-Weighted Citation Impact
- 0.00