IFIBYNE   05513
INSTITUTO DE FISIOLOGIA, BIOLOGIA MOLECULAR Y NEUROCIENCIAS
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
CONTRIBUTIONS OF THE PMC1, VCX1 AND YVC1 PATHWAYS TO CYTOSOLIC CALCIUM IN RESPONSE TO PHEROMONE
Autor/es:
AGUILAR, PABLO S; PONCE DAWSON, SILVINA; TARKOWSKI, NAHUEL
Lugar:
Parana
Reunión:
Congreso; LIV SAIB Annual Meeting; 2018
Institución organizadora:
SAIB
Resumen:
Saccharomyces cerevisiae haploid cells secrete mating pheromones that indicatethe presence of cells of one mating type to those of the oppositemating type. This initiates a sequence of events, which includes cellular arrest and growth polarization towards the secretory cell. Studiesshowed that the incorporation of calcium is necessary for cell survival and signal transduction to coordinate the genes involved. Studying thedynamics of calcium using microscopy and the fluorescent sensor GCaMP6f we found that pheromone does not generate a single elevation ofcytosolic ca2+ levels but transient increases in the form of bursts. Our results suggest that the information transmitted by calcium is encoded inthe temporal distribution of these bursts. Calcium uptake depends on at least two pathways, system HACS and system LACS. Through geneticmutations, we eliminated the activity of these pathways and we were able to observe the dependence with the temporal distributions of calciumbursts. We have proposed that the calcium response not only depends on transport pathways from the extracellular medium, but it can alsodepend on each of the different calcium flow pathways to and from each of the internal reservoirs. The aim of this work isto define the role ofcalcium transporters in internal reservoirs in response to pheromone. To address this, we monitored cells with mutated vacuolar Ca2+ ATPase(pmc1Δ), cell with mutated vacuolar membrane antiporter with Ca2+/H+ (vcx1Δ) and cell with mutated vacuolar channel (yvc1Δ). We arecurrently studying the variation of calcium burst distributions by eliminating the activity of these pathways through genetic mutations