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Highly modular bow-tie gene circuits with programmable dynamic behaviour

Author

Listed:
  • Laura Prochazka

    (Swiss Federal Institute of Technology (ETH) Zürich)

  • Bartolomeo Angelici

    (Swiss Federal Institute of Technology (ETH) Zürich)

  • Benjamin Haefliger

    (Swiss Federal Institute of Technology (ETH) Zürich)

  • Yaakov Benenson

    (Swiss Federal Institute of Technology (ETH) Zürich)

Abstract

Synthetic gene circuits often require extensive mutual optimization of their components for successful operation, while modular and programmable design platforms are rare. A possible solution lies in the ‘bow-tie’ architecture, which stipulates a focal component—a ‘knot’—uncoupling circuits’ inputs and outputs, simplifying component swapping, and introducing additional layer of control. Here we construct, in cultured human cells, synthetic bow-tie circuits that transduce microRNA inputs into protein outputs with independently programmable logical and dynamic behaviour. The latter is adjusted via two different knot configurations: a transcriptional activator causing the outputs to track input changes reversibly, and a recombinase-based cascade, converting transient inputs into permanent actuation. We characterize the circuits in HEK293 cells, confirming their modularity and scalability, and validate them using endogenous microRNA inputs in additional cell lines. This platform can be used for biotechnological and biomedical applications in vitro, in vivo and potentially in human therapy.

Suggested Citation

  • Laura Prochazka & Bartolomeo Angelici & Benjamin Haefliger & Yaakov Benenson, 2014. "Highly modular bow-tie gene circuits with programmable dynamic behaviour," Nature Communications, Nature, vol. 5(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms5729
    DOI: 10.1038/ncomms5729
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    Cited by:

    1. Charlotte Cautereels & Jolien Smets & Jonas De Saeger & Lloyd Cool & Yanmei Zhu & Anna Zimmermann & Jan Steensels & Anton Gorkovskiy & Thomas B. Jacobs & Kevin J. Verstrepen, 2024. "Orthogonal LoxPsym sites allow multiplexed site-specific recombination in prokaryotic and eukaryotic hosts," Nature Communications, Nature, vol. 15(1), pages 1-15, December.

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