Abstract

BackgroundCells sense chemical spatial gradients and respond by polarizing internal components. This process can be disrupted by gradient noise caused by fluctuations in chemical concentration.ResultsWe investigated how external gradient noise affects spatial sensing and response focusing on noise-filtering and the resultant tradeoffs. First, using a coarse-grained mathematical model of gradient-sensing and cell polarity, we characterized three negative consequences of noise: Inhibition of the extent of polarization, degradation of directional accuracy, and production of a noisy output polarization. Next, we explored filtering strategies and discovered that a combination of positive feedback, multiple signaling stages, and time-averaging produced good results. There was an important tradeoff, however, because filtering resulted in slower polarization. Simulations demonstrated that a two-stage filter-amplifier resulted in a balanced outcome. Then, we analyzed the effect of noise on a mechanistic model of yeast cell polarization in response to gradients of mating pheromone. This analysis showed that yeast cells likely also combine the above three filtering mechanisms into a filter-amplifier structure to achieve impressive spatial-noise tolerance, but with the consequence of a slow response time. Further investigation of the amplifier architecture revealed two positive feedback loops, a fast inner and a slow outer, both of which contributed to noise-tolerant polarization. This model also made specific predictions about how orientation performance depended upon the ratio between the gradient slope (signal) and the noise variance. To test these predictions, we performed microfluidics experiments measuring the ability of yeast cells to orient to shallow gradients of mating pheromone. The results of these experiments agreed well with the modeling predictions, demonstrating that yeast cells can sense gradients shallower than 0.1% μm-1, approximately a single receptor-ligand molecule difference between front and back, on par with motile eukaryotic cells.ConclusionsSpatial noise impedes the extent, accuracy, and smoothness of cell polarization. A combined filtering strategy implemented by a filter-amplifier architecture with slow dynamics was effective. Modeling and experimental data suggest that yeast cells employ these elaborate mechanisms to filter gradient noise resulting in a slow but relatively accurate polarization response.

Highlights

  • Cells sense chemical spatial gradients and respond by polarizing internal components

  • When we performed parametric analysis on k0 and k1, we identified two distinct dynamical regimes: A low positive feedback regime corresponding to ultrasensitive amplification and a high positive feedback regime corresponding to positive feedback amplification

  • One example was the yeast budding behavior in which the Bem1 positive feedback loop was fast and the Cdc42 actin loop was slow. These simulations were non-spatial, and here we explored spatial simulations in the context of cell polarity directed by an external cue

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Summary

Introduction

Cells sense chemical spatial gradients and respond by polarizing internal components. This process can be disrupted by gradient noise caused by fluctuations in chemical concentration. Cells sense and respond to external cues in a noisy environment [1]. These stimuli include light, nutrients, repellents, etc. Cells must filter the signal from noise, process the relevant information, and mount the appropriate response (e.g. moving, making a projection). For chemical signals such as an attractant, a cell. Several authors [5,6,7] have determined the properties of an optimal filter for separating signal from noise in temporal sensing

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