Abstract
Very little is known about how cellular osmosensors monitor changes in osmolarity of the environment. Here, we report that in yeast, Sln1 osmosensor histidine kinase monitors changes in turgor pressures. Reductions in turgor caused by either hyperosmotic stress, nystatin, or removal of cell wall activate MAPK Hog1 specifically through the SLN1 branch, but not through the SHO1 branch of the high osmolarity glycerol pathway. The integrity of the periplasmic region of Sln1 was essential for its sensor function. We found that activity of the plant histidine kinase cytokinin response 1 (Cre1) is also regulated by changes in turgor pressure, in a manner identical to that of Sln1, in the presence of cytokinin. We propose that Sln1 and Cre1 are turgor sensors, and that similar turgor-sensing mechanisms might regulate hyperosmotic stress responses both in yeast and plants.
MeSH Terms
Arabidopsis Proteins/metabolism
Cell Wall/metabolism
Cytokinins/metabolism,pharmacology
Glycerol/metabolism
Intracellular Signaling Peptides and Proteins
Intracranial Pressure/physiology
Mitogen-Activated Protein Kinases/metabolism
Nystatin/pharmacology
Osmotic Pressure
Protein Kinases/metabolism
Receptors, Cell Surface/metabolism
Saccharomyces cerevisiae/enzymology,genetics
Saccharomyces cerevisiae Proteins/metabolism
Water-Electrolyte Balance/physiology
Chemicals
Arabidopsis Proteins
Cytokinins
Intracellular Signaling Peptides and Proteins
Receptors, Cell Surface
Saccharomyces cerevisiae Proteins
Nystatin
Protein Kinases
HOG1 protein, S cerevisiae
Mitogen-Activated Protein Kinases
SLN1 protein, S cerevisiae
WOL protein, Arabidopsis
Glycerol
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Reiser VladimIr
Dana-Farber Cancer Institute, 44 Binney Street, Boston, MA 02115, USA.
Raitt Desmond C
Saito Haruo
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