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Conditional RNA interference in mammalian cells via RNA transactivation

Author

Listed:
  • Yu Zhou

    (UF Center for NeuroGenetics (CNG)
    University of Florida)

  • Peike Sheng

    (UF Center for NeuroGenetics (CNG)
    University of Florida
    UF Health Cancer Center)

  • Jiayi Li

    (Boston University
    Boston University)

  • Yudan Li

    (Boston University
    Boston University)

  • Mingyi Xie

    (UF Center for NeuroGenetics (CNG)
    University of Florida
    UF Health Cancer Center)

  • Alexander A. Green

    (Boston University
    Boston University
    Boston University)

Abstract

RNA interference (RNAi) is a powerful tool for sequence-specific gene knockdown in therapeutic and research applications. However, spatiotemporal control of RNAi is required to decrease nonspecific targeting, potential toxicity, and allow targeting of essential genes. Herein we describe a class of de-novo-designed RNA switches that enable sequence-specific regulation of RNAi in mammalian cells. Using cis-repressing RNA elements, we engineer RNA devices that only initiate microRNA biogenesis when binding with cognate trigger RNAs. We demonstrate that this conditional RNAi system, termed Orthogonal RNA Interference induced by Trigger RNA (ORIENTR), provides up to 14-fold increases in artificial miRNA biogenesis upon activation in orthogonal libraries. We show that integration of ORIENTR triggers with dCas13d enhances dynamic range to up to 31-fold. We further demonstrate that ORIENTR can be applied to detect endogenous RNA signals and to conditionally knockdown endogenous genes, thus enabling regulatory possibilities including cell-type-specific RNAi and rewiring of transcriptional networks via RNA profile.

Suggested Citation

  • Yu Zhou & Peike Sheng & Jiayi Li & Yudan Li & Mingyi Xie & Alexander A. Green, 2024. "Conditional RNA interference in mammalian cells via RNA transactivation," Nature Communications, Nature, vol. 15(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-50600-w
    DOI: 10.1038/s41467-024-50600-w
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