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 |
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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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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.</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 & 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. Jul 2002</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4734-5f993223cee410a8741164cfb96ab52c51a9d8a4b72f6133d55b04a92af0c7853</citedby><cites>FETCH-LOGICAL-c4734-5f993223cee410a8741164cfb96ab52c51a9d8a4b72f6133d55b04a92af0c7853</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1046%2Fj.1365-2958.2002.03024.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1046%2Fj.1365-2958.2002.03024.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12123456$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Palecek, Sean P.</creatorcontrib><creatorcontrib>Parikh, Archita S.</creatorcontrib><creatorcontrib>Huh, Joon H.</creatorcontrib><creatorcontrib>Kron, Stephen J.</creatorcontrib><title>Depression of Saccharomyces cerevisiae invasive growth on non‐glucose carbon sources requires the Snf1 kinase</title><title>Molecular microbiology</title><addtitle>Mol Microbiol</addtitle><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.</description><subject>Carbon - metabolism</subject><subject>Cell Adhesion</subject><subject>Cell Cycle Proteins - biosynthesis</subject><subject>Cell Cycle Proteins - genetics</subject><subject>Cell Polarity</subject><subject>Cell Wall - ultrastructure</subject><subject>Culture Media - chemistry</subject><subject>Culture Media - pharmacology</subject><subject>Cyclic AMP - physiology</subject><subject>Ethanol - pharmacology</subject><subject>Gene Expression Regulation, Fungal - drug effects</subject><subject>Glucose-6-Phosphate Isomerase - biosynthesis</subject><subject>Glucose-6-Phosphate Isomerase - genetics</subject><subject>Glycerol - pharmacology</subject><subject>Hexoses - pharmacology</subject><subject>Membrane Glycoproteins</subject><subject>Membrane Proteins - biosynthesis</subject><subject>Membrane Proteins - genetics</subject><subject>Protein-Serine-Threonine Kinases - genetics</subject><subject>Protein-Serine-Threonine Kinases - physiology</subject><subject>Raffinose - pharmacology</subject><subject>Saccharomyces cerevisiae - drug effects</subject><subject>Saccharomyces cerevisiae - enzymology</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Saccharomyces cerevisiae - growth & development</subject><subject>Saccharomyces cerevisiae - ultrastructure</subject><subject>Saccharomyces cerevisiae Proteins - genetics</subject><subject>Saccharomyces cerevisiae Proteins - physiology</subject><subject>Second Messenger Systems - drug effects</subject><issn>0950-382X</issn><issn>1365-2958</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkctu1DAUhi1ERYfCKyCLBbuE41sSL1iglkulVl0UJHaW4znpeMjEU3sy7ex4BJ6RJ8HpjEDqBlbHOv7-Xzr6CKEMSgayerssmahUwbVqSg7ASxDAZXn_hMz-fDwlM9AKCtHwb8fkeUpLACagEs_IMeOMC6mqGQlnuI6Ykg8DDR29ts4tbAyrncNEHUbc-uQtUj9sbfJbpDcx3G0WNONDGH79-HnTjy4kpM7GNi9TGOMUjXg7-lxMNwuk10PH6Hc_2IQvyFFn-4QvD_OEfP344cvp5-Li6tP56fuLwslayEJ1WgvOhUOUDGxTS8Yq6bpWV7ZV3Clm9byxsq15VzEh5kq1IK3mtgNXN0qckDf73nUMtyOmjVn55LDv7YBhTKZmmotGy3-CrJFSCqgz-PoRuMy3DvkIw3SleC6DDDV7yMWQUsTOrKNf2bgzDMykzizNZMhMhsykzjyoM_c5-urQP7YrnP8NHlxl4N0euPM97v672Fxenk8v8Rt9Bqjj</recordid><startdate>200207</startdate><enddate>200207</enddate><creator>Palecek, Sean P.</creator><creator>Parikh, Archita S.</creator><creator>Huh, Joon H.</creator><creator>Kron, Stephen J.</creator><general>Blackwell Science Ltd</general><general>Blackwell Publishing Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>200207</creationdate><title>Depression of Saccharomyces cerevisiae invasive growth on non‐glucose carbon sources requires the Snf1 kinase</title><author>Palecek, Sean P. ; Parikh, Archita S. ; Huh, Joon H. ; Kron, Stephen J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4734-5f993223cee410a8741164cfb96ab52c51a9d8a4b72f6133d55b04a92af0c7853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Carbon - metabolism</topic><topic>Cell Adhesion</topic><topic>Cell Cycle Proteins - biosynthesis</topic><topic>Cell Cycle Proteins - genetics</topic><topic>Cell Polarity</topic><topic>Cell Wall - ultrastructure</topic><topic>Culture Media - chemistry</topic><topic>Culture Media - pharmacology</topic><topic>Cyclic AMP - physiology</topic><topic>Ethanol - pharmacology</topic><topic>Gene Expression Regulation, Fungal - drug effects</topic><topic>Glucose-6-Phosphate Isomerase - biosynthesis</topic><topic>Glucose-6-Phosphate Isomerase - genetics</topic><topic>Glycerol - pharmacology</topic><topic>Hexoses - pharmacology</topic><topic>Membrane Glycoproteins</topic><topic>Membrane Proteins - biosynthesis</topic><topic>Membrane Proteins - genetics</topic><topic>Protein-Serine-Threonine Kinases - genetics</topic><topic>Protein-Serine-Threonine Kinases - physiology</topic><topic>Raffinose - pharmacology</topic><topic>Saccharomyces cerevisiae - drug effects</topic><topic>Saccharomyces cerevisiae - enzymology</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Saccharomyces cerevisiae - growth & development</topic><topic>Saccharomyces cerevisiae - ultrastructure</topic><topic>Saccharomyces cerevisiae Proteins - genetics</topic><topic>Saccharomyces cerevisiae Proteins - physiology</topic><topic>Second Messenger Systems - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Palecek, Sean P.</creatorcontrib><creatorcontrib>Parikh, Archita S.</creatorcontrib><creatorcontrib>Huh, Joon H.</creatorcontrib><creatorcontrib>Kron, Stephen J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Palecek, Sean P.</au><au>Parikh, Archita S.</au><au>Huh, Joon H.</au><au>Kron, Stephen J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Depression of Saccharomyces cerevisiae invasive growth on non‐glucose carbon sources requires the Snf1 kinase</atitle><jtitle>Molecular microbiology</jtitle><addtitle>Mol Microbiol</addtitle><date>2002-07</date><risdate>2002</risdate><volume>45</volume><issue>2</issue><spage>453</spage><epage>469</epage><pages>453-469</pages><issn>0950-382X</issn><eissn>1365-2958</eissn><abstract>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.</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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