Steady-state free Ca2+ in the yeast endoplasmic reticulum reaches only 10 microM and is mainly controlled by the secretory pathway pump Pmr1
Open Access
- 1 September 1999
- journal article
- research article
- Published by Springer Nature in The EMBO Journal
- Vol. 18 (17), 4733-4743
- https://doi.org/10.1093/emboj/18.17.4733
Abstract
Over recent decades, diverse intracellular organelles have been recognized as key determinants of Ca2+ signaling in eukaryotes. In yeast however, information on intra‐organellar Ca2+ concentrations is scarce, despite the demonstrated importance of Ca2+ signals for this microorganism. Here, we directly monitored free Ca2+ in the lumen of the endoplasmic reticulum (ER) of yeast cells, using a specifically targeted version of the Ca2+‐sensitive photoprotein aequorin. Ca2+ uptake into the yeast ER displayed characteristics distinctly different from the mammalian ER. At steady‐state, the free Ca2+ concentration in the ER lumen was limited to ∼10 μM, and ER Ca2+ sequestration was insensitive to thapsigargin, an inhibitor specific for mammalian ER Ca2+ pumps. In pmr1 null mutants, free Ca2+ in the ER was reduced by 50%. Our findings identify the secretory pathway pump Pmr1, predominantly localized in the Golgi, as a major component of ER Ca2+ uptake activity in yeast.Keywords
This publication has 39 references indexed in Scilit:
- Functional measurements of [Ca2+] in the endoplasmic reticulum using a herpes virus to deliver targeted aequorinCell Calcium, 1998
- Aequorin targeted to the endoplasmic reticulum reveals heterogeneity in luminal Ca++ concentration and reports agonist- or IP3-induced release of Ca++.Molecular Biology of the Cell, 1996
- Transfected Aequorin in the Measurement of Cytosolic Ca2+ Concentration ([Ca2+]c)Journal of Biological Chemistry, 1995
- Calcium signalingCell, 1995
- Calcineurin-dependent growth control in Saccharomyces cerevisiae mutants lacking PMC1, a homolog of plasma membrane Ca2+ ATPasesThe Journal of cell biology, 1994
- Inositol trisphosphate and calcium signallingNature, 1993
- The yeast Ca(2+)-ATPase homologue, PMR1, is required for normal Golgi function and localizes in a novel Golgi-like distribution.Molecular Biology of the Cell, 1992
- Topography of glycosylation in yeast: characterization of GDPmannose transport and lumenal guanosine diphosphatase activities in Golgi-like vesicles.Proceedings of the National Academy of Sciences, 1989
- Calcium transients in aequorin-injected frog cardiac muscleNature, 1978
- Aequorin Luminescence: Relation of Light Emission to Calcium Concentration—A Calcium-Independent ComponentScience, 1977