Control of adaptation to mating pheromone by G protein beta subunits of Saccharomyces cerevisiae
The STE4 gene of the yeast Saccharomyces cerevisiae encodes the beta subunit of a heterotrimeric G protein that mediates response to mating pheromones and influences recovery from pheromone-induced growth arrest. To explore how G(beta) subunits regulate response and recovery (adaptation), we isolate...
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Veröffentlicht in: | Genetics (Austin) 1994-12, Vol.138 (4), p.1081-1092 |
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description | The STE4 gene of the yeast Saccharomyces cerevisiae encodes the beta subunit of a heterotrimeric G protein that mediates response to mating pheromones and influences recovery from pheromone-induced growth arrest. To explore how G(beta) subunits regulate response and recovery (adaptation), we isolated and characterized signaling-defective STE4 alleles (STE4(sd)). STE4(sd) mutations resulted in amino acid substitutions in the N-terminal region of Ste4p, proximal to the first of seven repeat units conserved in G protein beta subunits. Genetic tests indicated that STE4(sd) mutations disrupted functions of Ste4p required for inducing pheromone responses. Wild-type cells that overexpressed STE4(sd) alleles displayed apparently normal initial responses to pheromone as judged by quantitative mating, G1 arrest and transcriptional assays. However, after undergoing initial G1 arrest, wild-type cells overexpressing STE4(sd) a,leles recovered more quickly from division arrest, suggestive of a hyperadaptive phenotype. Because hyperadaptation occurred when STE4(sd) alleles were overexpressed in cells lacking Sst1p (Bar1p), Sst2p or the C-terminal domain of the alpha-factor receptor, this phenotype did not involve three principal modes of adaptation in yeast. However, hyperadaptation was abolished when STE4(sd) mutations were combined in cis with a deletion that removes a segment of Ste4p (residues 310-346) previously implicated in adaptation to pheromone. These results indicate that G beta subunits possess two independent activities, one required for triggering pheromone response and another that promotes adaptation. Potential models for G beta subunit-mediated adaptation are discussed |
doi_str_mv | 10.1093/genetics/138.4.1081 |
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(Washington University School of Medicine, St. Louis, MO.) ; Weiner, J.L ; Blumer, K.J</creator><creatorcontrib>Grishin, A.V. (Washington University School of Medicine, St. Louis, MO.) ; Weiner, J.L ; Blumer, K.J</creatorcontrib><description>The STE4 gene of the yeast Saccharomyces cerevisiae encodes the beta subunit of a heterotrimeric G protein that mediates response to mating pheromones and influences recovery from pheromone-induced growth arrest. To explore how G(beta) subunits regulate response and recovery (adaptation), we isolated and characterized signaling-defective STE4 alleles (STE4(sd)). STE4(sd) mutations resulted in amino acid substitutions in the N-terminal region of Ste4p, proximal to the first of seven repeat units conserved in G protein beta subunits. Genetic tests indicated that STE4(sd) mutations disrupted functions of Ste4p required for inducing pheromone responses. Wild-type cells that overexpressed STE4(sd) alleles displayed apparently normal initial responses to pheromone as judged by quantitative mating, G1 arrest and transcriptional assays. However, after undergoing initial G1 arrest, wild-type cells overexpressing STE4(sd) a,leles recovered more quickly from division arrest, suggestive of a hyperadaptive phenotype. Because hyperadaptation occurred when STE4(sd) alleles were overexpressed in cells lacking Sst1p (Bar1p), Sst2p or the C-terminal domain of the alpha-factor receptor, this phenotype did not involve three principal modes of adaptation in yeast. However, hyperadaptation was abolished when STE4(sd) mutations were combined in cis with a deletion that removes a segment of Ste4p (residues 310-346) previously implicated in adaptation to pheromone. These results indicate that G beta subunits possess two independent activities, one required for triggering pheromone response and another that promotes adaptation. Potential models for G beta subunit-mediated adaptation are discussed</description><identifier>ISSN: 0016-6731</identifier><identifier>ISSN: 1943-2631</identifier><identifier>EISSN: 1943-2631</identifier><identifier>DOI: 10.1093/genetics/138.4.1081</identifier><identifier>PMID: 7896092</identifier><identifier>CODEN: GENTAE</identifier><language>eng</language><publisher>United States: Genetics Society of America</publisher><subject>ACCOUPLEMENT ; ADAPTACION ; ADAPTATION ; Adaptation, Physiological ; Amino Acid Sequence ; Base Sequence ; COMPOSICION QUIMICA ; COMPOSITION CHIMIQUE ; COPULA ; FENOTIPOS ; FEROMONAS ; Fungal Proteins - genetics ; Fungal Proteins - physiology ; GENE ; GENES ; Genetics ; GTP-Binding Protein beta Subunits ; GTP-Binding Proteins - physiology ; Heterotrimeric GTP-Binding Proteins ; Investigations ; Mating Factor ; Molecular Sequence Data ; MUTACION INDUCIDA ; MUTANT ; MUTANTES ; MUTATION PROVOQUEE ; NUCLEOTIDE ; NUCLEOTIDOS ; Peptides - genetics ; Peptides - physiology ; PHENOTYPE ; PHEROMONE ; PROTEINAS AGLUTINANTES ; PROTEINE DE LIAISON ; Proteins ; SACCHAROMYCES CEREVISIAE ; Saccharomyces cerevisiae - genetics ; Saccharomyces cerevisiae - physiology ; Saccharomyces cerevisiae Proteins ; Signal Transduction ; Yeast</subject><ispartof>Genetics (Austin), 1994-12, Vol.138 (4), p.1081-1092</ispartof><rights>Copyright Genetics Society of America Dec 1994</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c477t-50b028c0b7314f838eff5f63c627acac6e70fb7621886194d43bb085d46e90863</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,778,782,883,27907,27908</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7896092$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Grishin, A.V. (Washington University School of Medicine, St. Louis, MO.)</creatorcontrib><creatorcontrib>Weiner, J.L</creatorcontrib><creatorcontrib>Blumer, K.J</creatorcontrib><title>Control of adaptation to mating pheromone by G protein beta subunits of Saccharomyces cerevisiae</title><title>Genetics (Austin)</title><addtitle>Genetics</addtitle><description>The STE4 gene of the yeast Saccharomyces cerevisiae encodes the beta subunit of a heterotrimeric G protein that mediates response to mating pheromones and influences recovery from pheromone-induced growth arrest. To explore how G(beta) subunits regulate response and recovery (adaptation), we isolated and characterized signaling-defective STE4 alleles (STE4(sd)). STE4(sd) mutations resulted in amino acid substitutions in the N-terminal region of Ste4p, proximal to the first of seven repeat units conserved in G protein beta subunits. Genetic tests indicated that STE4(sd) mutations disrupted functions of Ste4p required for inducing pheromone responses. Wild-type cells that overexpressed STE4(sd) alleles displayed apparently normal initial responses to pheromone as judged by quantitative mating, G1 arrest and transcriptional assays. However, after undergoing initial G1 arrest, wild-type cells overexpressing STE4(sd) a,leles recovered more quickly from division arrest, suggestive of a hyperadaptive phenotype. Because hyperadaptation occurred when STE4(sd) alleles were overexpressed in cells lacking Sst1p (Bar1p), Sst2p or the C-terminal domain of the alpha-factor receptor, this phenotype did not involve three principal modes of adaptation in yeast. However, hyperadaptation was abolished when STE4(sd) mutations were combined in cis with a deletion that removes a segment of Ste4p (residues 310-346) previously implicated in adaptation to pheromone. These results indicate that G beta subunits possess two independent activities, one required for triggering pheromone response and another that promotes adaptation. Potential models for G beta subunit-mediated adaptation are discussed</description><subject>ACCOUPLEMENT</subject><subject>ADAPTACION</subject><subject>ADAPTATION</subject><subject>Adaptation, Physiological</subject><subject>Amino Acid Sequence</subject><subject>Base Sequence</subject><subject>COMPOSICION QUIMICA</subject><subject>COMPOSITION CHIMIQUE</subject><subject>COPULA</subject><subject>FENOTIPOS</subject><subject>FEROMONAS</subject><subject>Fungal Proteins - genetics</subject><subject>Fungal Proteins - physiology</subject><subject>GENE</subject><subject>GENES</subject><subject>Genetics</subject><subject>GTP-Binding Protein beta Subunits</subject><subject>GTP-Binding Proteins - physiology</subject><subject>Heterotrimeric GTP-Binding Proteins</subject><subject>Investigations</subject><subject>Mating Factor</subject><subject>Molecular Sequence Data</subject><subject>MUTACION INDUCIDA</subject><subject>MUTANT</subject><subject>MUTANTES</subject><subject>MUTATION PROVOQUEE</subject><subject>NUCLEOTIDE</subject><subject>NUCLEOTIDOS</subject><subject>Peptides - genetics</subject><subject>Peptides - physiology</subject><subject>PHENOTYPE</subject><subject>PHEROMONE</subject><subject>PROTEINAS AGLUTINANTES</subject><subject>PROTEINE DE LIAISON</subject><subject>Proteins</subject><subject>SACCHAROMYCES CEREVISIAE</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Saccharomyces cerevisiae - physiology</subject><subject>Saccharomyces cerevisiae Proteins</subject><subject>Signal Transduction</subject><subject>Yeast</subject><issn>0016-6731</issn><issn>1943-2631</issn><issn>1943-2631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUU1rFDEYDqLUtfoHFCF46G3afE0mcxFksVUoeKg9xyT7zm7KTDImmcL-e7PsWtSLIZCQ54P3yYPQO0ouKen51RYCFO_yFeXqUtQ3RZ-hFe0Fb5jk9DlaEUJlIztOX6JXOT8QQmTfqjN01qlekp6t0I91DCXFEccBm42Ziyk-BlwinuotbPG8gxSnGADbPb7Bc4oFfMAWisF5sUvwJR_Ed8a5nanUvYOMHSR49NkbeI1eDGbM8OZ0nqP768_f11-a2283X9efbhsnuq40LbGEKUdsHVYMiisYhnaQ3EnWGWechI4MtpOMKiVrxI3g1hLVboSEnijJz9HHo--82Ak2DmosM-o5-cmkvY7G67-R4Hd6Gx81ZUQy0VeDi5NBij8XyEVPPjsYRxMgLll3dQle9_-IVKpWCt5W4od_iA9xSaH-gmZUUMYoObjxI8mlmHOC4WlkSvShZv27Zl1r1kIfaq6q93-mfdKceq342yM-mKjNNvms7-_6litGFP8FWkKvHg</recordid><startdate>19941201</startdate><enddate>19941201</enddate><creator>Grishin, A.V. (Washington University School of Medicine, St. Louis, MO.)</creator><creator>Weiner, J.L</creator><creator>Blumer, K.J</creator><general>Genetics Society of America</general><scope>FBQ</scope><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>4T-</scope><scope>4U-</scope><scope>7QP</scope><scope>7SS</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7QR</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19941201</creationdate><title>Control of adaptation to mating pheromone by G protein beta subunits of Saccharomyces cerevisiae</title><author>Grishin, A.V. (Washington University School of Medicine, St. Louis, MO.) ; Weiner, J.L ; Blumer, K.J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c477t-50b028c0b7314f838eff5f63c627acac6e70fb7621886194d43bb085d46e90863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>ACCOUPLEMENT</topic><topic>ADAPTACION</topic><topic>ADAPTATION</topic><topic>Adaptation, Physiological</topic><topic>Amino Acid Sequence</topic><topic>Base Sequence</topic><topic>COMPOSICION QUIMICA</topic><topic>COMPOSITION CHIMIQUE</topic><topic>COPULA</topic><topic>FENOTIPOS</topic><topic>FEROMONAS</topic><topic>Fungal Proteins - genetics</topic><topic>Fungal Proteins - physiology</topic><topic>GENE</topic><topic>GENES</topic><topic>Genetics</topic><topic>GTP-Binding Protein beta Subunits</topic><topic>GTP-Binding Proteins - physiology</topic><topic>Heterotrimeric GTP-Binding Proteins</topic><topic>Investigations</topic><topic>Mating Factor</topic><topic>Molecular Sequence Data</topic><topic>MUTACION INDUCIDA</topic><topic>MUTANT</topic><topic>MUTANTES</topic><topic>MUTATION PROVOQUEE</topic><topic>NUCLEOTIDE</topic><topic>NUCLEOTIDOS</topic><topic>Peptides - genetics</topic><topic>Peptides - physiology</topic><topic>PHENOTYPE</topic><topic>PHEROMONE</topic><topic>PROTEINAS AGLUTINANTES</topic><topic>PROTEINE DE LIAISON</topic><topic>Proteins</topic><topic>SACCHAROMYCES CEREVISIAE</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Saccharomyces cerevisiae - physiology</topic><topic>Saccharomyces cerevisiae Proteins</topic><topic>Signal Transduction</topic><topic>Yeast</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Grishin, A.V. 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(Washington University School of Medicine, St. Louis, MO.)</au><au>Weiner, J.L</au><au>Blumer, K.J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Control of adaptation to mating pheromone by G protein beta subunits of Saccharomyces cerevisiae</atitle><jtitle>Genetics (Austin)</jtitle><addtitle>Genetics</addtitle><date>1994-12-01</date><risdate>1994</risdate><volume>138</volume><issue>4</issue><spage>1081</spage><epage>1092</epage><pages>1081-1092</pages><issn>0016-6731</issn><issn>1943-2631</issn><eissn>1943-2631</eissn><coden>GENTAE</coden><abstract>The STE4 gene of the yeast Saccharomyces cerevisiae encodes the beta subunit of a heterotrimeric G protein that mediates response to mating pheromones and influences recovery from pheromone-induced growth arrest. To explore how G(beta) subunits regulate response and recovery (adaptation), we isolated and characterized signaling-defective STE4 alleles (STE4(sd)). STE4(sd) mutations resulted in amino acid substitutions in the N-terminal region of Ste4p, proximal to the first of seven repeat units conserved in G protein beta subunits. Genetic tests indicated that STE4(sd) mutations disrupted functions of Ste4p required for inducing pheromone responses. Wild-type cells that overexpressed STE4(sd) alleles displayed apparently normal initial responses to pheromone as judged by quantitative mating, G1 arrest and transcriptional assays. However, after undergoing initial G1 arrest, wild-type cells overexpressing STE4(sd) a,leles recovered more quickly from division arrest, suggestive of a hyperadaptive phenotype. Because hyperadaptation occurred when STE4(sd) alleles were overexpressed in cells lacking Sst1p (Bar1p), Sst2p or the C-terminal domain of the alpha-factor receptor, this phenotype did not involve three principal modes of adaptation in yeast. However, hyperadaptation was abolished when STE4(sd) mutations were combined in cis with a deletion that removes a segment of Ste4p (residues 310-346) previously implicated in adaptation to pheromone. These results indicate that G beta subunits possess two independent activities, one required for triggering pheromone response and another that promotes adaptation. Potential models for G beta subunit-mediated adaptation are discussed</abstract><cop>United States</cop><pub>Genetics Society of America</pub><pmid>7896092</pmid><doi>10.1093/genetics/138.4.1081</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | ACCOUPLEMENT ADAPTACION ADAPTATION Adaptation, Physiological Amino Acid Sequence Base Sequence COMPOSICION QUIMICA COMPOSITION CHIMIQUE COPULA FENOTIPOS FEROMONAS Fungal Proteins - genetics Fungal Proteins - physiology GENE GENES Genetics GTP-Binding Protein beta Subunits GTP-Binding Proteins - physiology Heterotrimeric GTP-Binding Proteins Investigations Mating Factor Molecular Sequence Data MUTACION INDUCIDA MUTANT MUTANTES MUTATION PROVOQUEE NUCLEOTIDE NUCLEOTIDOS Peptides - genetics Peptides - physiology PHENOTYPE PHEROMONE PROTEINAS AGLUTINANTES PROTEINE DE LIAISON Proteins SACCHAROMYCES CEREVISIAE Saccharomyces cerevisiae - genetics Saccharomyces cerevisiae - physiology Saccharomyces cerevisiae Proteins Signal Transduction Yeast |
title | Control of adaptation to mating pheromone by G protein beta subunits of Saccharomyces cerevisiae |
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