Intracellular calcium is a second messenger involved in several processes in yeast, such as mating, nutrient sensing, stress response and cell cycle events. It was reported that glucose addition stimulates a rapid increase in free calcium level in yeast. To investigate the calcium level variations induced by different stimuli we used a reporter system based on the photoprotein aequorin. Glucose addition (50 mM) to nutrient-starved cells induced an increase in free intracellular calcium concentration, mainly due to an influx from external medium. The increase of calcium reached its maximum 100-120 s after the stimulus. A concentration of about 20 mM glucose was required for a 50% increase in intracellular calcium. This response was completely abolished in strain plc1Δ and in the isogenic wild-type strain treated with 3-nitrocoumarin, a phosphatidylinositol-specific phospholipase C inhibitor, suggesting that Plc1p is essential for glucose-induced calcium increase. This suggests that Plc1p should have a significant role in transducing glucose signal. The calcium influx induced by addition of high glucose on cells previously stimulated with low glucose levels was inhibited in strains with a deletion in the GPR1 or GPA2 genes, which suggests that glucose would be detected through the Gpr1p/Gpa2p receptor/G protein-coupled (GPCR) complex. Moreover, the signal was completely abolished in a strain unable to phosphorylate glucose, which is consistent with the reported requirement of glucose phosphorylation for GPCR complex activation. © 2002 Published by Elsevier Science B.V. on behalf of the Federation of European Biochemical Societies.

Tisi, R., Baldassa, S., Belotti, F., Martegani, E. (2002). Phospholipase C is required for glucose-induced calcium influx in budding yeast. FEBS LETTERS, 520(1-3), 133-138 [10.1016/s0014-5793(02)02806-5].

Phospholipase C is required for glucose-induced calcium influx in budding yeast

Tisi, Renata
Primo
;
Belotti, Fiorella
Penultimo
;
Martegani, Enzo
Ultimo
2002

Abstract

Intracellular calcium is a second messenger involved in several processes in yeast, such as mating, nutrient sensing, stress response and cell cycle events. It was reported that glucose addition stimulates a rapid increase in free calcium level in yeast. To investigate the calcium level variations induced by different stimuli we used a reporter system based on the photoprotein aequorin. Glucose addition (50 mM) to nutrient-starved cells induced an increase in free intracellular calcium concentration, mainly due to an influx from external medium. The increase of calcium reached its maximum 100-120 s after the stimulus. A concentration of about 20 mM glucose was required for a 50% increase in intracellular calcium. This response was completely abolished in strain plc1Δ and in the isogenic wild-type strain treated with 3-nitrocoumarin, a phosphatidylinositol-specific phospholipase C inhibitor, suggesting that Plc1p is essential for glucose-induced calcium increase. This suggests that Plc1p should have a significant role in transducing glucose signal. The calcium influx induced by addition of high glucose on cells previously stimulated with low glucose levels was inhibited in strains with a deletion in the GPR1 or GPA2 genes, which suggests that glucose would be detected through the Gpr1p/Gpa2p receptor/G protein-coupled (GPCR) complex. Moreover, the signal was completely abolished in a strain unable to phosphorylate glucose, which is consistent with the reported requirement of glucose phosphorylation for GPCR complex activation. © 2002 Published by Elsevier Science B.V. on behalf of the Federation of European Biochemical Societies.
Articolo in rivista - Articolo scientifico
Aequorin; Glucose signalling; PLC1; Polyphosphoinositide turnover;
English
2002
520
1-3
133
138
reserved
Tisi, R., Baldassa, S., Belotti, F., Martegani, E. (2002). Phospholipase C is required for glucose-induced calcium influx in budding yeast. FEBS LETTERS, 520(1-3), 133-138 [10.1016/s0014-5793(02)02806-5].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/568501
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