Abstract

Site-specific recombinases (SSRs) mediate efficient manipulation of DNA sequences in vitro and in vivo. In particular, serine integrases have been identified as highly effective tools for facilitating DNA inversion, enabling the design of genetic switches that are capable of turning the expression of a gene of interest on or off in the presence of a SSR protein. The functional scope of such circuitry can be extended to biological Boolean logic operations by incorporating two or more distinct integrase inputs. To date, mathematical modelling investigations have captured the dynamical properties of integrase logic gate systems in a purely qualitative manner, and thus such models are of limited utility as tools in the design of novel circuitry. Here, the authors develop a detailed mechanistic model of a two-input temporal logic gate circuit that can detect and encode sequences of input events. Their model demonstrates quantitative agreement with time-course data on the dynamics of the temporal logic gate, and is shown to subsequently predict dynamical responses relating to a series of induction separation intervals. The model can also be used to infer functional variations between distinct integrase inputs, and to examine the effect of reversing the roles of each integrase on logic gate output.

Highlights

  • 1.1 Engineering cellular memory using DNA recombinationGenetic switches form the basis of engineered cellular memory [1, 2]

  • It is comprised of both red fluorescent protein (RFP) and green fluorescent protein (GFP) levels under eight distinct experimental conditions

  • We assume that RFP and GFP provide a direct readout of the DNA state of the system that equates to the concentration levels required to parameterise our model

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Summary

Introduction

1.1 Engineering cellular memory using DNA recombinationGenetic switches form the basis of engineered cellular memory [1, 2]. The characterisation of the genetic toggle switch in Escherichia coli [6] triggered the advent of synthetic biology, demonstrating that user-defined functionality can be engineered in biological systems Such circuits are highly orthogonal with regard to assembling multiplexed systems [7]; regulating gene expression in this manner has limitations. Research on the engineering of cellular memory in synthetic biology has become increasingly centred around site-specific recombinases (SSRs), which are capable of precise DNA manipulation both in vitro and in vivo [10]. This process, known as DNA recombination, facilitates inducible gene expression that is programmed into the cellular DNA. DNA-based systems are promising for the engineering of cellular memory devices since they exploit a natural data storage material and have the added advantage of eliminating cell specificity requirements

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