Association of putative ammonium exporters Ato with detergent-resistant compartments of plasma membrane during yeast colony development: pH affects Ato1p localisation in patches
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
17395151
DOI
10.1016/j.bbamem.2007.02.011
PII: S0005-2736(07)00041-7
Knihovny.cz E-resources
- MeSH
- Ammonia metabolism MeSH
- Cell Membrane metabolism MeSH
- Detergents metabolism MeSH
- Cell Compartmentation * MeSH
- Hydrogen-Ion Concentration MeSH
- Quaternary Ammonium Compounds metabolism MeSH
- Membrane Proteins metabolism MeSH
- Membrane Transport Proteins metabolism MeSH
- Recombinant Fusion Proteins metabolism MeSH
- Saccharomyces cerevisiae Proteins metabolism MeSH
- Saccharomyces cerevisiae cytology metabolism MeSH
- Protein Transport MeSH
- Green Fluorescent Proteins metabolism MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Ammonia MeSH
- ATO1 protein, S cerevisiae MeSH Browser
- ATO2 protein, S cerevisiae MeSH Browser
- ATO3 protein, S cerevisiae MeSH Browser
- Detergents MeSH
- Quaternary Ammonium Compounds MeSH
- Membrane Proteins MeSH
- Membrane Transport Proteins MeSH
- Recombinant Fusion Proteins MeSH
- Saccharomyces cerevisiae Proteins MeSH
- Green Fluorescent Proteins MeSH
It was proposed that Ato1p, Ato2p and Ato3p have a role in ammonia production by Saccharomyces cerevisiae colonies (Palkova et al., Mol Biol Cell 13: 3901-3914, 2002). In this study, we show that all three Ato proteins localise to the plasma membrane and their appearance correlates with the beginning of ammonia release. The expression of ATO genes is controlled by ammonia. All three Ato-GFP proteins associate with detergent-resistant membranes; two of them, Ato1p-GFP and Ato3p-GFP, localise to patches visible under the fluorescence microscope. In contrast with Ato3p-GFP which forms stable patches, the formation of those of Ato1p-GFP is pH dependent. Ato1p-GFP patches form at pH above 6 and they disappear at pH 5 or lower. Both changes, Ato1p-GFP clustering and patches spreading are reversible. The Ato1p-GFP spreading at low pH is independent on endocytosis. These data suggest that besides the ammonia induction of Ato protein synthesis, pH may rapidly regulate Ato1p function.
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