Rational design of a small molecule-responsive intramer controlling transgene expression in mammalian cells.

Nucleic Acids Res

ETH Zurich, Department of Biosystems Science and Bioengineering (D-BSSE), Mattenstrasse 26, CH-4058 Basel, Switzerland.

Published: December 2011

AI Article Synopsis

  • Aptamers can effectively build artificial genetic switches by targeting proteins or small molecules.
  • The study introduces a new aptamer-based system that regulates the Tet Off system independent of tetracycline, allowing control of gene expression in mammalian cells.
  • By utilizing theophylline as a ligand, researchers enhanced binding to the aptamer, leading to decreased activity of the transactivator and enabling more complex gene network designs.

Article Abstract

Aptamers binding proteins or small molecules have been shown to be versatile and powerful building blocks for the construction of artificial genetic switches. In this study, we present a novel aptamer-based construct regulating the Tet Off system in a tetracycline-independent manner thus achieving control of transgene expression. For this purpose, a TetR protein-inhibiting aptamer was engineered for use in mammalian cells, enabling the RNA-responsive control of the tetracycline-dependent transactivator (tTA). By rationally attaching the theophylline aptamer as a sensor, the inhibitory TetR aptamer and thus tTA activity became dependent on the ligand of the sensor aptamer. Addition of the small molecule theophylline resulted in enhanced binding to the corresponding protein in vitro and in inhibition of reporter gene expression in mammalian cell lines. By using aptamers as adaptors in order to control protein activity by a predetermined small molecule, we present a simple and straightforward approach for future applications in the field of Chemical Biology. Moreover, aptamer-based control of the widely used Tet system introduces a new layer of regulation thereby facilitating the construction of more complex gene networks.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3239198PMC
http://dx.doi.org/10.1093/nar/gkr829DOI Listing

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