Activation of an essential calcium signaling pathway in Saccharomyces cerevisiae by Kch1 and Kch2, putative low-affinity potassium transporters

TitleActivation of an essential calcium signaling pathway in Saccharomyces cerevisiae by Kch1 and Kch2, putative low-affinity potassium transporters
Publication TypeJournal Article
Year of Publication2013
AuthorsStefan CP, Zhang N, Sokabe T, Rivetta A, Slayman CL, Montell C, Cunningham KW
JournalEukaryot Cell
Volume12
Pagination204-14
Date Published2013 Feb
ISSN1535-9786
KeywordsCalcium Channels, Calcium Chloride, Calcium Signaling, Cation Transport Proteins, Gene Expression, Gene Knockout Techniques, HEK293 Cells, Humans, Hydrogen-Ion Concentration, Membrane Potentials, Patch-Clamp Techniques, Peptides, Potassium, Protein Transport, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins
Abstract

In the budding yeast Saccharomyces cerevisiae, mating pheromones activate a high-affinity Ca(2+) influx system (HACS) that activates calcineurin and is essential for cell survival. Here we identify extracellular K(+) and a homologous pair of transmembrane proteins, Kch1 and Kch2 (Prm6), as necessary components of the HACS activation mechanism. Expression of Kch1 and especially Kch2 was strongly induced during the response to mating pheromones. When forcibly overexpressed, Kch1 and Kch2 localized to the plasma membrane and activated HACS in a fashion that depended on extracellular K(+) but not pheromones. They also promoted growth of trk1 trk2 mutant cells in low K(+) environments, suggesting they promote K(+) uptake. Voltage-clamp recordings of protoplasts revealed diminished inward K(+) currents in kch1 kch2 double-mutant cells relative to the wild type. Conversely, heterologous expression of Kch1 in HEK293T cells caused the appearance of inwardly rectifying K(+) currents. Collectively, these findings suggest that Kch1 and Kch2 directly promote K(+) influx and that HACS may electrochemically respond to K(+) influx in much the same way as the homologous voltage-gated Ca(2+) channels in most animal cell types.

DOI10.1128/EC.00299-12
Alternate JournalEukaryotic Cell
PubMed ID23204190
PubMed Central IDPMC3571297
Grant ListEY10852 / EY / NEI NIH HHS / United States
GM053082 / GM / NIGMS NIH HHS / United States
GM085335 / GM / NIGMS NIH HHS / United States
GM60696 / GM / NIGMS NIH HHS / United States
NS074072 / NS / NINDS NIH HHS / United States