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Mutational analysis of putative phosphate- and proton-binding sites in the Saccharomyces cerevisiae Pho84 phosphate:H+ transceptor and its effect on signalling to the PKA and PHO pathways

Samyn, Dieter R. (författare)
Linnéuniversitetet,Institutionen för naturvetenskap, NV,Bengt Persson,School of Natural Sciences, Linnaeus University, Kalmar, Sweden
Ruiz-Pavon, Lorena (författare)
Linnéuniversitetet,Institutionen för naturvetenskap, NV,Bengt Persson,School of Natural Sciences, Linnaeus University, Kalmar, Sweden
Andersson, Michael R. (författare)
Linnéuniversitetet,Institutionen för naturvetenskap, NV,Bengt Persson,School of Natural Sciences, Linnaeus University, Kalmar, Sweden
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Popova, Yulia (författare)
Laboratory of Molecular Cell Biology, Institute of Botany and Microbiology, Katholieke Universiteit Leuven, Leuven-Heverlee, Belgium; Department of Molecular Microbiology, Vlaams Interuniversitair Instituut Voor Biotechnologie (VIB), Leuven-Heverlee, Belgium
Thevelein, Johan (författare)
Laboratory of Molecular Cell Biology, Institute of Botany and Microbiology, Katholieke Universiteit Leuven, Leuven-Heverlee, Belgium; Department of Molecular Microbiology, Vlaams Interuniversitair Instituut Voor Biotechnologie (VIB), Leuven-Heverlee, Belgium
Persson, Bengt L. (författare)
Linnéuniversitetet,Institutionen för naturvetenskap, NV,Bengt Persson,School of Natural Sciences, Linnaeus University, Kalmar, Sweden; Laboratory of Molecular Cell Biology, Institute of Botany and Microbiology, Katholieke Universiteit Leuven, Leuven-Heverlee, Belgium; Department of Molecular Microbiology, Vlaams Interuniversitair Instituut Voor Biotechnologie (VIB), Leuven-Heverlee, Belgium
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 (creator_code:org_t)
Portland Press, 2012
2012
Engelska.
Ingår i: Biochemical Journal. - : Portland Press. - 0264-6021 .- 1470-8728. ; 445, s. 413-422
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • In Saccharomyces cerevisiae, the Pho84 phosphate transporter acts as the main provider of phosphate to the cell using a proton symport mechanism, but also mediates rapid activation of the PKA (protein kinase A) pathway. These two features led to recognition of Pho84 as a transceptor. Although the physiological role of Pho84 has been studied in depth, the mechanisms underlying the transport and sensor functions are unclear. To obtain more insight into the structure–function relationships of Pho84, we have rationally designed and analysed site-directed mutants. Using a three-dimensional model of Pho84 created on the basis of the GlpT permease, complemented with multiple sequence alignments, we selected Arg168 and Lys492, and Asp178, Asp358 and Glu473 as residues potentially involved in phosphate or proton binding respectively, during transport. We found that Asp358 (helix 7) and Lys492 (helix 11) are critical for the transport function, and might be part of the putative substrate-binding pocket of Pho84. Moreover, we show that alleles mutated in the putative proton-binding site Asp358 are still capable of strongly activating PKA pathway targets, despite their severely reduced transport activity. This indicates that signalling does not require transport and suggests that mutagenesis of amino acid residues involved in binding of the co-transported ion may constitute a promising general approach to separate the transport and signalling functions in transceptors.

Ämnesord

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Nyckelord

Pho84
phosphate binding
phosphate transport
protein kinase A
proton binding
Saccharomyces cerevisiae
transceptor.
Biokemi
Biochemistry

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