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Sensitive detection of proteasomal activation using the Deg-On mammalian synthetic gene circuit

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Listed:
  • Wenting Zhao

    (Rice University)

  • Matthew Bonem

    (Rice University)

  • Claire McWhite

    (Rice University)

  • Jonathan J. Silberg

    (Rice University)

  • Laura Segatori

    (Rice University
    Rice University
    Rice University)

Abstract

The ubiquitin proteasome system (UPS) has emerged as a drug target for diverse diseases characterized by altered proteostasis, but pharmacological agents that enhance UPS activity have been challenging to establish. Here we report the Deg-On system, a genetic inverter that translates proteasomal degradation of the transcriptional regulator TetR into a fluorescent signal, thereby linking UPS activity to an easily detectable output, which can be tuned using tetracycline. We demonstrate that this circuit responds to modulation of UPS activity in cell culture arising from the inhibitor MG-132 and activator PA28γ. Guided by predictive modelling, we enhanced the circuit’s signal sensitivity and dynamic range by introducing a feedback loop that enables self-amplification of TetR. By linking UPS activity to a simple and tunable fluorescence output, these genetic inverters will enable a variety of applications, including screening for UPS activating molecules and selecting for mammalian cells with different levels of proteasome activity.

Suggested Citation

  • Wenting Zhao & Matthew Bonem & Claire McWhite & Jonathan J. Silberg & Laura Segatori, 2014. "Sensitive detection of proteasomal activation using the Deg-On mammalian synthetic gene circuit," Nature Communications, Nature, vol. 5(1), pages 1-12, May.
    • Handle: RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms4612
    DOI: 10.1038/ncomms4612
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