Gene regulation, phenotypic memory, and selection in fluctuating environments

Gene regulatory networks enable bacteria to sense and respond in fluctuating environments and to control gene expression levels in constant conditions. Despite substantial advances in understanding their molecular biology, the evolutionary conditions that select for and maintain gene regulatory networks have remained elusive. Here, we investigate the evolutionary costs and benefits of gene regulation under metabolic fluctuations, and identify distinct fluctuating environments that select for or against gene regulation. Using barcode sequencing to track strain frequencies over time, we compete strains with perturbed expression dynamics to assess the strength of selection on gene expression levels. We reveal that expression levels can be shaped to enhance phenotypic memory of past environmental states, reducing the impact of lag phases on long-term population growth. By independently perturbing the ability to sense the environment and the control of expression levels, we discover sign epistasis between sensing and control in a gene regulatory network, and identify its molecular underpinnings. Due to this epistatic interaction, maintenance of sensing in gene regulation enhances the ability of evolution to tune gene expression in a fluctuating environment. Our work establishes a new basis for understanding how gene regulatory networks evolve in fluctuating environments.