Local Pheromone Release from Dynamic Polarity Sites Underlies Cell-Cell Pairing during Yeast Mating

Autor: Sophie G. Martin, Felipe O. Bendezú, Laura Merlini, Bita Khalili, Daniel Hurwitz, Dimitrios Vavylonis, Vincent Vincenzetti
Rok vydání: 2016
Předmět:
0301 basic medicine
education
Biophysics
CDC42
Saccharomyces cerevisiae
Biology
Pheromones
General Biochemistry
Genetics and Molecular Biology

Article
Cell Fusion
03 medical and health sciences
Botany
Cell polarity
Schizosaccharomyces
ATP-Binding Cassette Transporters/metabolism
Cell Polarity
Pheromones/metabolism
Schizosaccharomyces/cytology
Schizosaccharomyces/physiology
Schizosaccharomyces pombe Proteins/chemistry
Schizosaccharomyces pombe Proteins/metabolism
Signal Transduction
cdc42 GTP-Binding Protein/metabolism
cdc42 GTP-Binding Protein
health care economics and organizations
Cell Membrane
biology.organism_classification
Cell biology
030104 developmental biology
Mating of yeast
Pairing
Sex pheromone
Schizosaccharomyces pombe
Pheromone
ATP-Binding Cassette Transporters
Schizosaccharomyces pombe Proteins
Signal transduction
General Agricultural and Biological Sciences
Zdroj: Current biology, vol. 26, no. 8, pp. 1117-1125
ISSN: 0006-3495
DOI: 10.1016/j.bpj.2015.11.817
Popis: Cell pairing is central for many processes, including immune defense, neuronal connection, hyphal fusion, and sexual reproduction. How does a cell orient toward a partner, especially when faced with multiple choices? Fission yeast Schizosaccharomyces pombe P and M cells, which respectively express P and M factor pheromones [1, 2], pair during the mating process induced by nitrogen starvation. Engagement of pheromone receptors Map3 and Mam2 [3, 4] with their cognate pheromone ligands leads to activation of the Gα protein Gpa1 to signal sexual differentiation [3, 5, 6]. Prior to cell pairing, the Cdc42 GTPase, a central regulator of cell polarization, forms dynamic zones of activity at the cell periphery at distinct locations over time [7]. Here we show that Cdc42-GTP polarization sites contain the M factor transporter Mam1, the general secretion machinery, which underlies P factor secretion, and Gpa1, suggesting that these are sub-cellular zones of pheromone secretion and signaling. Zone lifetimes scale with pheromone concentration. Computational simulations of pair formation through a fluctuating zone show that the combination of local pheromone release and sensing, short pheromone decay length, and pheromone-dependent zone stabilization leads to efficient pair formation. Consistently, pairing efficiency is reduced in the absence of the P factor protease. Similarly, zone stabilization at reduced pheromone levels, which occurs in the absence of the predicted GTPase-activating protein for Ras, leads to reduction in pairing efficiency. We propose that efficient cell pairing relies on fluctuating local signal emission and perception, which become locked into place through stimulation.
Databáze: OpenAIRE