Association of putative ammonium exporters Ato with detergent-resistant compartments of plasma membrane during yeast colony development: pH affects Ato1p localisation in patches
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
17395151
DOI
10.1016/j.bbamem.2007.02.011
PII: S0005-2736(07)00041-7
Knihovny.cz E-zdroje
- MeSH
- amoniak metabolismus MeSH
- buněčná membrána metabolismus MeSH
- detergenty metabolismus MeSH
- kompartmentace buňky * MeSH
- koncentrace vodíkových iontů MeSH
- kvartérní amoniové sloučeniny metabolismus MeSH
- membránové proteiny metabolismus MeSH
- membránové transportní proteiny metabolismus MeSH
- rekombinantní fúzní proteiny metabolismus MeSH
- Saccharomyces cerevisiae - proteiny metabolismus MeSH
- Saccharomyces cerevisiae cytologie metabolismus MeSH
- transport proteinů MeSH
- zelené fluorescenční proteiny metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- amoniak MeSH
- ATO1 protein, S cerevisiae MeSH Prohlížeč
- ATO2 protein, S cerevisiae MeSH Prohlížeč
- ATO3 protein, S cerevisiae MeSH Prohlížeč
- detergenty MeSH
- kvartérní amoniové sloučeniny MeSH
- membránové proteiny MeSH
- membránové transportní proteiny MeSH
- rekombinantní fúzní proteiny MeSH
- Saccharomyces cerevisiae - proteiny MeSH
- zelené fluorescenční proteiny 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.
Citace poskytuje Crossref.org
General and molecular microbiology and microbial genetics in the IM CAS