Abstract

Gene expression heterogeneity is a key driver for microbial adaptation to fluctuating environmental conditions, cell differentiation and the evolution of species. This phenomenon has therefore enormous implications, not only for life in general, but also for biotechnological applications where unwanted subpopulations of non-producing cells can emerge in large-scale fermentations. Only time-lapse fluorescence microscopy allows real-time measurements of gene expression heterogeneity. A major limitation in the analysis of time-lapse microscopy data is the lack of fast, cost-effective, open, simple and adaptable protocols. Here we describe TLM-Quant, a semi-automatic pipeline for the analysis of time-lapse fluorescence microscopy data that enables the user to visualize and quantify gene expression heterogeneity. Importantly, our pipeline builds on the open-source packages ImageJ and R. To validate TLM-Quant, we selected three possible scenarios, namely homogeneous expression, highly ‘noisy’ heterogeneous expression, and bistable heterogeneous expression in the Gram-positive bacterium Bacillus subtilis. This bacterium is both a paradigm for systems-level studies on gene expression and a highly appreciated biotechnological ‘cell factory’. We conclude that the temporal resolution of such analyses with TLM-Quant is only limited by the numbers of recorded images.

Highlights

  • Microorganisms need to adapt to environmental changes by appropriately adjusting their gene expression [1]

  • In recent years it has become increasingly clear that the expression of particular genes is often not uniform in the individual cells of a microbial population, even when these cells are grown under carefully controlled conditions

  • For studies in B. subtilis, we have implemented an amyE::Pspac-GFPmut2 strain in which homogeneous Green Fluorescent Protein (GFP) expression can be set at different levels by growing the cells in the presence of different IPTG concentrations

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Summary

Introduction

Microorganisms need to adapt to environmental changes by appropriately adjusting their gene expression [1]. There can be considerable noise or heterogeneity in the expression levels of individual genes, and secondly, there can even be situations of bistability where particular genes are only transcribed in a sub-population of the analysed cells. To investigate gene expression heterogeneity in different cells of growing populations, alternative approaches are needed, such as flow cytometry and time-lapse microscopy.

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