Biology subjects

Garcia-Alcala, M.

Publications and source records attributed to Garcia-Alcala, M..

3 recordsLinked to original sources

bioRxiv2024

Stochastic Growth Bursts Enable Burden-Free Flagellum Production in a Single Bacterium

The cost of expressing unnecessary genes on growth has been explained at the population level through balanced growth assumptions. However, due to the high degree of stochasticity in growth and gene regulation, it remains unclear how classical growth laws derived from bulk measurements manifest at the level of individual cells. For example, flagellar gene expression, one of the most energy-intensive processes in E. coli, is typically associated with reduced growth rates in bulk measurements. By contrast, we find at the single-cell level that a strikingly opposite behavior coexists: flagellar gene activity is associated with an increase in growth rate. We show that this apparent contradiction, reminiscent of Simpsons paradox, results from examining in each cell instantaneous growth and gene expression without indiscriminately aggregating the single-cell data like in bulk measurements. We attribute this unrecognized behavior to out-of-balance growth boosts that temporarily offset the burden of flagellum production, likely driven by a surplus of growth factors inherited across cell division. Furthermore, we show that this non-intuitive relationship between growth and gene expression at the single-cell level is general, as we observe similar effects with synthetic systems driving the expression of fluorescent proteins downstream of constitutive promoters. Finally, we use a computational model to show that the inheritance of parental growth factors can explain the apparent contradiction and constitutes a general mechanism for mitigating the short-term cost of nonessential and biosynthetically demanding genes in the single cell.

molecular biology↗

bioRxiv2021

Robustness of DNA Looping Across Multiple Divisions in Individual Bacteria

DNA looping has emerged as a central paradigm of transcriptional regulation as it is shared across many living systems. One core property of DNA looping-based regulation is its ability to greatly enhance repression or activation of genes with only a few copies of transcriptional regulators. However, this property based on small number of proteins raises the question of the robustness of such a mechanism with respect to the large intracellular perturbations taking place during growth and division of the cell. Here we address the issue of sensitivity to variations of intracellular parameters of gene regulation by DNA looping. We use the lac system as a prototype to experimentally identify the key features of the robustness of DNA looping in growing E. coli cells. Surprisingly, we observe time intervals of tight repression spanning across division events, which can sometimes exceed ten generations. Remarkably, the distribution of such long time intervals exhibits memoryless statistics that is mostly insensitive to repressor concentration, cell division events, and the number of distinct loops accessible to the system. By contrast, gene regulation becomes highly sensitive to these perturbations when DNA looping is absent. Using stochastic simulations, we propose that the robustness to division events of memoryless distributions emerges from the competition between fast, multiple re-binding events of repressors and slow initiation rate of the RNA-polymerase. We argue that fast re-binding events are a direct consequence of DNA looping that ensures robust gene repression across a range of intracellular perturbations. Significance statementIt is well-established that certain intracellular regulators can stabilize DNA loops to greatly enhance activation or repression of gene transcription. In vitro but also in vivo ensemble measurements have determined that only a few copies of regulators are in fact needed to stably form DNA loops. In view of such a small number, we address the issue of sensitivity of gene regulation by DNA looping to variations of intracellular parameters in individual growing E. coli bacteria. Surprisingly, we find that DNA looping from the lac system is robust to a range of perturbations including divisions during which cells can maintain tight repression over many generations. We propose a mechanism that governs the observed robustness across a range of intracellular perturbations.

biophysics↗

bioRxiv2020

A filter-and-integrate mechanism generates stochastictranscriptional pulses in E.coli flagellar synthesis

Stochastic pulsatile dynamics have been observed in an increasing number of biological circuits with typical mechanism involving feedback control. Surprisingly, recent single-cell experiments showed that E. coli flagellar class-2&3 promoters are activated in stochastic pulses without the means of feedback, however, the underlying design principles of pulse generation have remained unclear. Here, by developing a system-level stochastic model constrained by a large set of E. coli flagellar synthesis data from different strains and mutants, we identify the underlying design principles for generating stochastic transcriptional pulses without feedback. Our model shows that YdiV, an inhibitor of the class-1 master regulator (FlhDC), creates an ultrasensitve switch that serves as a digital filter to eliminate small amplitude FlhDC fluctuations. Additionally, we demonstrate that fast temporal fluctuations of FlhDC are smoothed out and integrated over time before affecting class-2 downstream genes. Together, our results reveal the existence of a filter-and-integrate design that is necessary for generating stochastic pulses without feedback. This strategy suggests that E. coli may avoid premature activation of the expensive flagellar gene expression by filtering input fluctuations in intensity and in time.

microbiology↗