| Literature DB >> 34050026 |
Debraj Ghose1,2, Katherine Jacobs2, Samuel Ramirez3, Timothy Elston3, Daniel Lew4.
Abstract
How small eukaryotic cells can interpret dynamic, noisy, and spatially complex chemical gradients to orient growth or movement is poorly understood. We address this question using Saccharomyces cerevisiae, where cells orient polarity up pheromone gradients during mating. Initial orientation is often incorrect, but polarity sites then move around the cortex in a search for partners. We find that this movement is biased by local pheromone gradients across the polarity site: that is, movement of the polarity site is chemotactic. A bottom-up computational model recapitulates this biased movement. The model reveals how even though pheromone-bound receptors do not mimic the shape of external pheromone gradients, nonlinear and stochastic effects combine to generate effective gradient tracking. This mechanism for gradient tracking may be applicable to any cell that searches for a target in a complex chemical landscape.Entities:
Keywords: cell polarity; chemotropism; modeling; pheromone; yeast
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Year: 2021 PMID: 34050026 PMCID: PMC8179161 DOI: 10.1073/pnas.2025445118
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205