A 'resource allocator' for transcription based on a highly fragmented T7 RNA polymerase

Thomas H. Segall-Shapiro, Adam J. Meyer, Andrew D. Ellington, Eduardo D. Sontag, Christopher A. Voigt

Research output: Contribution to journalArticlepeer-review

94 Scopus citations

Abstract

Synthetic genetic systems share resources with the host, including machinery for transcription and translation. Phage RNA polymerases (RNAPs) decouple transcription from the host and generate high expression. However, they can exhibit toxicity and lack accessory proteins (σ factors and activators) that enable switching between different promoters and modulation of activity. Here, we show that T7 RNAP (883 amino acids) can be divided into four fragments that have to be co-expressed to function. The DNA-binding loop is encoded in a C-terminal 285-aa 'σ fragment', and fragments with different specificity can direct the remaining 601-aa 'core fragment' to different promoters. Using these parts, we have built a resource allocator that sets the core fragment concentration, which is then shared by multiple σ fragments. Adjusting the concentration of the core fragment sets the maximum transcriptional capacity available to a synthetic system. Further, positive and negative regulation is implemented using a 67-aa N-terminal 'α fragment' and a null (inactivated) σ fragment, respectively. The α fragment can be fused to recombinant proteins to make promoters responsive to their levels. These parts provide a toolbox to allocate transcriptional resources via different schemes, which we demonstrate by building a system which adjusts promoter activity to compensate for the difference in copy number of two plasmids.

Original languageEnglish (US)
Article number742
JournalMolecular Systems Biology
Volume10
Issue number7
DOIs
StatePublished - Jul 2014

All Science Journal Classification (ASJC) codes

  • Biochemistry, Genetics and Molecular Biology(all)
  • Immunology and Microbiology(all)
  • Agricultural and Biological Sciences(all)
  • Applied Mathematics

Keywords

  • T7 RNA polymerase
  • genetic circuit
  • resource allocation
  • split protein
  • synthetic biology

Fingerprint Dive into the research topics of 'A 'resource allocator' for transcription based on a highly fragmented T7 RNA polymerase'. Together they form a unique fingerprint.

Cite this