Abstract
The molecular makeup of the offspring of a dividing cell gradually becomes phenotypically decorrelated from the parent cell by noise and regulatory mechanisms that amplify phenotypic heterogeneity. Such regulatory mechanisms form networks that contain thresholds between phenotypes. Populations of cells can be poised near the threshold so that a subset of the population probabilistically undergoes the phenotypic transition. We sought to characterize the diversity of bacterial populations around a growth-modulating threshold via analysis of the effect of non-genetic inheritance, similar to conditions that create antibiotictolerant persister cells and other examples of bet hedging. Using simulations and experimental lineage data in Escherichia coli, we present evidence that regulation of growth amplifies the dependence of growth arrest on cellular lineage, causing clusters of related cells undergo growth arrest in certain conditions. Our simulations predict that lineage correlations and the sensitivity of growth to changes in toxin levels coincide in a critical regime. Below the critical regime, the sizes of related growth arrested clusters are distributed exponentially, while in the critical regime clusters sizes are more likely to become large. Furthermore, phenotypic diversity can be nearly as high as possible near the critical regime, but for most parameter values it falls far below the theoretical limit. We conclude that lineage information is indispensable for understanding regulation of cellular growth.
Author Summary One of the most important characteristics of a cell is whether it is growing. Actively growing cells can multiply exponentially. In the case of infections and cancer, growth causes problems for the host organism. On the other hand, cells that have stopped growing can allocate cellular resources toward different activities, such as bacteria surviving antibiotics and tissues in multicellular organisms performing their physiological roles. Observing small bacterial colonies in a microscope over time, we have found that cells closely related to each other often have similar growth state. We were curious if lineage dependence was an intrinsic property of growth regulation or if other factors were needed to explain this effect. We therefore built a computational model of a growing and dividing cellular colony with an encoded growth regulation network. We found that regulation of growth is sufficient for lineage dependence to emerge. We next asked if lineage dependence constrains how diverse the cellular population can become. We found that cellular diversity can reach a peak that is nearly as high as possible near the conditions that have the highest lineage dependence, but that most conditions do not permit such high diversity. We conclude that lineage is an important constraint and discuss how the growth arrest transition is in some ways like a phase transition from physics, and in some ways strikingly different, making it a unique phenomenon.
