Abstract
The yeast YPR192w gene, which encodes a protein (Aqy1p) with strong homology to aquaporins (AQPs), was cloned from nine S. cerevisiae strains. The osmotic water permeability coefficient (Pf) of X. laevis oocytes expressing the gene cloned from the Sigma1278b strain (AQY1-1) was 5.7 times higher than the Pf of oocytes expressing the gene cloned from other strains (AQY1-2). Aqy1-1p, initially cloned without its C-terminus (Aqy1-1DeltaCp), mediated an approximately 3 times higher water permeability than the full-length protein. This corresponds to a 3-fold higher protein density in the oocyte plasma membrane, as shown by freeze-fracture electron microscopy. Pf measurements in yeast spheroplasts confirmed the presence of functional water channels in Sigma1278b and a pharmacological study indicated that this strain contains at least a second functional aquaporin.
Copyright 1999 Academic Press.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Animals
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Aquaporins / chemistry
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Aquaporins / genetics
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Aquaporins / metabolism*
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Blotting, Western
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Cell Membrane / metabolism
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Cell Membrane / ultrastructure
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Cell Membrane Permeability / drug effects
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Cloning, Molecular
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Fungal Proteins / chemistry
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Fungal Proteins / metabolism
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Glycerol / metabolism
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Mercuric Chloride / pharmacology
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Molecular Sequence Data
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Oocytes / cytology
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Oocytes / metabolism
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Oocytes / ultrastructure
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Osmolar Concentration
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Saccharomyces cerevisiae / drug effects
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Saccharomyces cerevisiae / metabolism*
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Saccharomyces cerevisiae Proteins*
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Sequence Deletion
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Sorbitol / metabolism
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Spheroplasts / drug effects
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Spheroplasts / metabolism
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Temperature
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Urea / metabolism
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Water / metabolism
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Xenopus laevis
Substances
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AQY1 protein, S cerevisiae
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Aquaporins
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Fungal Proteins
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Saccharomyces cerevisiae Proteins
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Water
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Sorbitol
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Mercuric Chloride
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Urea
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Glycerol