Orthogonal inducible control of Cas13 circuits enables programmable RNA regulation in mammalian cells

Yage Ding, Cristina Tous, Jaehoon Choi, Jingyao Chen and Wilson W. Wong ()
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Yage Ding: Boston University
Cristina Tous: Boston University
Jaehoon Choi: Boston University
Jingyao Chen: Boston University
Wilson W. Wong: Boston University

Nature Communications, 2024, vol. 15, issue 1, 1-16

Abstract: Abstract RNA plays an indispensable role in mammalian cell functions. Cas13, a class of RNA-guided ribonuclease, is a flexible tool for modifying and regulating coding and non-coding RNAs, with enormous potential for creating new cell functions. However, the lack of control over Cas13 activity has limited its cell engineering capability. Here, we present the CRISTAL (Control of RNA with Inducible SpliT CAs13 Orthologs and Exogenous Ligands) platform. CRISTAL is powered by a collection (10 total) of orthogonal split inducible Cas13 effectors that can be turned ON or OFF via small molecules in multiple cell types, providing precise temporal control. Also, we engineer Cas13 logic circuits that can respond to endogenous signaling and exogenous small molecule inputs. Furthermore, the orthogonality, low leakiness, and high dynamic range of our inducible Cas13d and Cas13b enable the design and construction of a robust incoherent feedforward loop, leading to near-perfect and tunable adaptation response. Finally, using our inducible Cas13 effectors, we achieve simultaneous multiplexed control of multiple genes in vitro and in mice. Together, our CRISTAL design represents a powerful platform for precisely regulating RNA dynamics to advance cell engineering and elucidate RNA biology.

Date: 2024
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DOI: 10.1038/s41467-024-45795-x

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