Abstract
Disruption of genes encoding endogenous transport proteins in Saccharomyces cerevisiae has facilitated the recent cloning, by functional expression, of cDNAs encoding K+ channels and amino acid transporters from the plant Arabidopsis thaliana [1-4]. In the present study, we demonstrate in whole-cell patch clamp experiments that the inability of trk1deltatrk2delta mutants of S. cerevisiae to grow on submillimolar K+ correlates with the lack of K+ inward currents, which are present in wild-type cells, and that transformation of the trk1deltatrk2delta double-deletion mutant with KAT1 from Arabidopsis thaliana restores this phenotype by encoding a plasma membrane protein that allows large K+ inward currents. Similar K+ inward currents are induced by transformation of a trk1 mutant with AKT1 from A. thaliana.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
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Arabidopsis
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Arabidopsis Proteins*
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Carrier Proteins / genetics
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Cation Transport Proteins*
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Fungal Proteins / genetics
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Genes, Plant
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Genetic Complementation Test
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Homeodomain Proteins / genetics
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Homeodomain Proteins / physiology
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Ion Transport
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Kinesins*
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Membrane Proteins / genetics
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Patch-Clamp Techniques
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Plant Proteins / genetics
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Plant Proteins / physiology*
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Potassium / metabolism*
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Potassium Channels / genetics
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Potassium Channels / physiology*
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Potassium Channels, Inwardly Rectifying*
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Saccharomyces cerevisiae / genetics
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Saccharomyces cerevisiae / physiology*
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Saccharomyces cerevisiae Proteins*
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Sequence Deletion
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Trans-Activators / genetics
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Trans-Activators / physiology
Substances
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ATK1 protein, Arabidopsis
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Arabidopsis Proteins
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Carrier Proteins
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Cation Transport Proteins
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Fungal Proteins
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Homeodomain Proteins
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KAT1 protein, Arabidopsis
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Membrane Proteins
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Plant Proteins
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Potassium Channels
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Potassium Channels, Inwardly Rectifying
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Saccharomyces cerevisiae Proteins
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TRK2 protein, S cerevisiae
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Trans-Activators
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TRK1 protein, S cerevisiae
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Kinesins
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Potassium