An intersectional expression platform for gene complementation using RNA-fragment end joining (REJ)
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Gene complementation is a powerful tool for genetic selection and protein functional studies but typically requires extensive screening for complementary components. Here we engineered a platform for gene complementation based on RNA end-joining (REJ) that precisely and efficiently splices separate RNA units into functional coding mRNAs. REJ is mediated by short structured modular RNA segments of ∼250bp that: (a) promote RNA::RNA interaction, (b) coopt the intrinsic cell splicing machinery to facilitate RNA trans-splicing, (c) minimizes translation of protein fragments from un-spliced RNA segments, and (d) encodes scar-free protein. We demonstrate that REJ is a broadly applicable system that can reliably split nearly any gene into complementary segments regardless of protein structure. To enable the use of this system we provide a toolbox of reporters and a web-based design tool to facilitate vector design. Demonstrated REJ applications include genetic complementation, intersectional labeling of cell types, and efficient expression of large proteins.
Highlights
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Synthetic RNA cis-elements can direct efficient and precise RNA trans-splicing in vivo .
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Endogenous splicing factors catalyze RNA end-joining (REJ) without foreign proteins.
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The REJ platform can be applied to nearly any gene with few positional constraints.
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REJ can be used as an intersectional tool to build complex genetic logic circuits.