Depression of Saccharomyces cerevisiae invasive growth on non‐glucose carbon sources requires the Snf1 kinase

Summary Haploid Saccharomyces cerevisiae cells growing on media lacking glucose but containing high concentrations of carbon sources such as fructose, galactose, raffinose, and ethanol exhibit enhanced agar invasion. These carbon sources also promote diploid filamentous growth in response to nitroge...

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Veröffentlicht in:Molecular microbiology 2002-07, Vol.45 (2), p.453-469
Hauptverfasser: Palecek, Sean P., Parikh, Archita S., Huh, Joon H., Kron, Stephen J.
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creator Palecek, Sean P.
Parikh, Archita S.
Huh, Joon H.
Kron, Stephen J.
description Summary Haploid Saccharomyces cerevisiae cells growing on media lacking glucose but containing high concentrations of carbon sources such as fructose, galactose, raffinose, and ethanol exhibit enhanced agar invasion. These carbon sources also promote diploid filamentous growth in response to nitrogen starvation. The enhanced invasive and filamentous growth phenotypes are suppressed by the addition of glucose to the media and require the Snf1 kinase. Mutations in the PGI1 and GND1 genes encoding carbon source utilization enzymes confer enhanced invasive growth that is unaffected by glucose but requires active Snf1. Carbon source does not modulate FLO11 flocculin expression, but enhanced polarized bud site selection is necessary for invasion on certain carbon sources. Interestingly, deletion of SNF1 blocks invasion without affecting bud site selection. Snf1 is also required for formation of spokes and hubs in multicellular mats. To examine glucose repression of invasive growth more broadly, we performed genome‐wide microarray expression analysis in wild‐type cells growing on glucose and galactose, and snf1Δ cells on galactose. SNF1 probably mediates glucose repression of multiple genes potentially involved in invasive and filamentous growth. FLO11‐independent cell‐cell attachment, cell wall integrity, and/or polarized growth are affected by carbon source metabolism. In addition, derepression of cell cycle genes and signalling via the cAMP–PKA pathway appears to depend upon SNF1 activity during growth on galactose.
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These carbon sources also promote diploid filamentous growth in response to nitrogen starvation. The enhanced invasive and filamentous growth phenotypes are suppressed by the addition of glucose to the media and require the Snf1 kinase. Mutations in the PGI1 and GND1 genes encoding carbon source utilization enzymes confer enhanced invasive growth that is unaffected by glucose but requires active Snf1. Carbon source does not modulate FLO11 flocculin expression, but enhanced polarized bud site selection is necessary for invasion on certain carbon sources. Interestingly, deletion of SNF1 blocks invasion without affecting bud site selection. Snf1 is also required for formation of spokes and hubs in multicellular mats. To examine glucose repression of invasive growth more broadly, we performed genome‐wide microarray expression analysis in wild‐type cells growing on glucose and galactose, and snf1Δ cells on galactose. SNF1 probably mediates glucose repression of multiple genes potentially involved in invasive and filamentous growth. FLO11‐independent cell‐cell attachment, cell wall integrity, and/or polarized growth are affected by carbon source metabolism. In addition, derepression of cell cycle genes and signalling via the cAMP–PKA pathway appears to depend upon SNF1 activity during growth on galactose.</description><identifier>ISSN: 0950-382X</identifier><identifier>EISSN: 1365-2958</identifier><identifier>DOI: 10.1046/j.1365-2958.2002.03024.x</identifier><identifier>PMID: 12123456</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Carbon - metabolism ; Cell Adhesion ; Cell Cycle Proteins - biosynthesis ; Cell Cycle Proteins - genetics ; Cell Polarity ; Cell Wall - ultrastructure ; Culture Media - chemistry ; Culture Media - pharmacology ; Cyclic AMP - physiology ; Ethanol - pharmacology ; Gene Expression Regulation, Fungal - drug effects ; Glucose-6-Phosphate Isomerase - biosynthesis ; Glucose-6-Phosphate Isomerase - genetics ; Glycerol - pharmacology ; Hexoses - pharmacology ; Membrane Glycoproteins ; Membrane Proteins - biosynthesis ; Membrane Proteins - genetics ; Protein-Serine-Threonine Kinases - genetics ; Protein-Serine-Threonine Kinases - physiology ; Raffinose - pharmacology ; Saccharomyces cerevisiae - drug effects ; Saccharomyces cerevisiae - enzymology ; Saccharomyces cerevisiae - genetics ; Saccharomyces cerevisiae - growth &amp; development ; Saccharomyces cerevisiae - ultrastructure ; Saccharomyces cerevisiae Proteins - genetics ; Saccharomyces cerevisiae Proteins - physiology ; Second Messenger Systems - drug effects</subject><ispartof>Molecular microbiology, 2002-07, Vol.45 (2), p.453-469</ispartof><rights>Copyright Blackwell Scientific Publications Ltd. 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These carbon sources also promote diploid filamentous growth in response to nitrogen starvation. The enhanced invasive and filamentous growth phenotypes are suppressed by the addition of glucose to the media and require the Snf1 kinase. Mutations in the PGI1 and GND1 genes encoding carbon source utilization enzymes confer enhanced invasive growth that is unaffected by glucose but requires active Snf1. Carbon source does not modulate FLO11 flocculin expression, but enhanced polarized bud site selection is necessary for invasion on certain carbon sources. Interestingly, deletion of SNF1 blocks invasion without affecting bud site selection. Snf1 is also required for formation of spokes and hubs in multicellular mats. To examine glucose repression of invasive growth more broadly, we performed genome‐wide microarray expression analysis in wild‐type cells growing on glucose and galactose, and snf1Δ cells on galactose. SNF1 probably mediates glucose repression of multiple genes potentially involved in invasive and filamentous growth. FLO11‐independent cell‐cell attachment, cell wall integrity, and/or polarized growth are affected by carbon source metabolism. 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SNF1 probably mediates glucose repression of multiple genes potentially involved in invasive and filamentous growth. FLO11‐independent cell‐cell attachment, cell wall integrity, and/or polarized growth are affected by carbon source metabolism. In addition, derepression of cell cycle genes and signalling via the cAMP–PKA pathway appears to depend upon SNF1 activity during growth on galactose.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>12123456</pmid><doi>10.1046/j.1365-2958.2002.03024.x</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record>
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subjects Carbon - metabolism
Cell Adhesion
Cell Cycle Proteins - biosynthesis
Cell Cycle Proteins - genetics
Cell Polarity
Cell Wall - ultrastructure
Culture Media - chemistry
Culture Media - pharmacology
Cyclic AMP - physiology
Ethanol - pharmacology
Gene Expression Regulation, Fungal - drug effects
Glucose-6-Phosphate Isomerase - biosynthesis
Glucose-6-Phosphate Isomerase - genetics
Glycerol - pharmacology
Hexoses - pharmacology
Membrane Glycoproteins
Membrane Proteins - biosynthesis
Membrane Proteins - genetics
Protein-Serine-Threonine Kinases - genetics
Protein-Serine-Threonine Kinases - physiology
Raffinose - pharmacology
Saccharomyces cerevisiae - drug effects
Saccharomyces cerevisiae - enzymology
Saccharomyces cerevisiae - genetics
Saccharomyces cerevisiae - growth & development
Saccharomyces cerevisiae - ultrastructure
Saccharomyces cerevisiae Proteins - genetics
Saccharomyces cerevisiae Proteins - physiology
Second Messenger Systems - drug effects
title Depression of Saccharomyces cerevisiae invasive growth on non‐glucose carbon sources requires the Snf1 kinase
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