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A Riboswitch-Based inducible gene expression system for mycobacteria

  • Jessica C. Seeliger
  • , Shana Topp
  • , Kimberly M. Sogi
  • , Mary L. Previti
  • , Justin P. Gallivan
  • , Carolyn R. Bertozzi
  • University of California at Berkeley
  • Stony Brook University
  • Emory University

Research output: Contribution to journalArticlepeer-review

58 Scopus citations

Abstract

Research on the human pathogen Mycobacterium tuberculosis (Mtb) would benefit from novel tools for regulated gene expression. Here we describe the characterization and application of a synthetic riboswitch-based system, which comprises a mycobacterial promoter for transcriptional control and a riboswitch for translational control. The system was used to induce and repress heterologous protein overexpression reversibly, to create a conditional gene knockdown, and to control gene expression in a macrophage infection model. Unlike existing systems for controlling gene expression in Mtb, the riboswitch does not require the co-expression of any accessory proteins: all of the regulatory machinery is encoded by a short DNA segment directly upstream of the target gene. The inducible riboswitch platform has the potential to be a powerful general strategy for creating customized gene regulation systems in Mtb.

Original languageEnglish
Article numbere29266
JournalPLoS ONE
Volume7
Issue number1
DOIs
StatePublished - Jan 18 2012

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