Abstract

The control of gene expression is an important tool for metabolic engineering, the design of synthetic gene networks, and protein manufacturing. The most successful approaches to date are based on modulating mRNA synthesis via an inducible coupling to transcriptional effectors. Here we present a biological programming structure that leverages a system of engineered transcription factors and complementary genetic architectures. We use a modular design strategy to create 27 non-natural and non-synonymous transcription factors using the lactose repressor topology as a guide. To direct systems of engineered transcription factors we employ parallel and series genetic (DNA) architectures and confer fundamental and combinatorial logical control over gene expression. Here we achieve AND, OR, NOT, and NOR logical controls in addition to two non-canonical half-AND operations. The basic logical operations and corresponding parallel and series genetic architectures represent the building blocks for subsequent combinatorial programs, which display both digital and analog performance.

Highlights

  • The control of gene expression is an important tool for metabolic engineering, the design of synthetic gene networks, and protein manufacturing

  • In this study we introduce a biological programming edifice based on an engineered system of non-natural transcription factors and complementary genetic architectures

  • Given that the engineered transcription factors are adapted with alternate DNA recognition and operator DNA elements that are not represented in nature, the resulting logical operations can be constructed and operated alongside existing natural genetic programs

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Summary

Introduction

The control of gene expression is an important tool for metabolic engineering, the design of synthetic gene networks, and protein manufacturing. To direct systems of engineered transcription factors we employ parallel and series genetic (DNA) architectures and confer fundamental and combinatorial logical control over gene expression. TFs are DNA-binding proteins capable of blocking (or recruiting) RNA polymerase activity at the site of genetic promoters, and these functions can be combined in modular ways to engineer synthetic gene networks[31]. In the presence of the chemical signal isopropyl-β-D-thiogalactoside or IPTG (a nonhydrolyzable analog of the natural inducer 1,6-allolactose) LacI undergoes a conformational shift that results in decreased affinity for its cognate DNA operator. This event allows transcription of the downstream gene to proceed[35]. The functional unit of LacI is a dimer, residues 331–360 make up the C-terminal tetramerization domain which facilitates the dimerization of two functional units[36,37,38,39]

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