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Antagonistic control of a dual-input mammalian gene switch by food additives

  • Mingqi Xie
  • , Haifeng Ye
  • , Ghislaine Charpin-El Hamri
  • , Martin Fussenegger*
  • *此作品的通讯作者
  • Swiss Federal Institute of Technology Zurich
  • Institut Universitaire de Technologie
  • University of Basel

科研成果: 期刊稿件文章同行评审

摘要

Synthetic biology has significantly advanced the design of mammalian trigger-inducible transgene-control devices that are able to programme complex cellular behaviour. Fruit-based benzoate derivatives licensed as food additives, such as flavours (e.g. vanillate) and preservatives (e.g. benzoate), are a particularly attractive class of trigger compounds for orthogonalmammalian transgene control devices because of their innocuousness, physiological compatibility and simple oral administration. Capitalizing on the genetic componentry of the soil bacterium Comamonas testosteroni, which has evolved to catabolize a variety of aromatic compounds, we have designed different mammalian gene expression systems that could be induced and repressed by the food additives benzoate and vanillate. When implanting designer cells engineered for gene switch-driven expression of the human placental secreted alkaline phosphatase (SEAP) into mice, blood SEAP levels of treated animals directly correlated with a benzoate-enriched drinking programme. Additionally, the benzoate-/vanillate-responsive device was compatible with other transgene control systems and could be assembled into higher-order control networks providing expression dynamics reminiscent of a lap-timing stopwatch. Designer gene switches using licensed food additives as trigger compounds to achieve antagonistic dual-input expression profiles and provide novel control topologies and regulation dynamics may advance future gene- and cell-based therapies.

源语言英语
页(从-至)e116
期刊Nucleic Acids Research
42
14
DOI
出版状态已出版 - 18 8月 2014

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