Saturation mutagenesis of the yeast his3 regulatory site: requirements for transcriptional induction and for binding by GCN4 activator protein
Expression of the yeast his3 and other amino acid biosynthetic genes is induced during conditions of amino acid starvation. The coordination of this response is mediated by a positive regulatory protein called GCN4, which binds specifically to regulatory sites upstream of all coregulated genes and s...
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Veröffentlicht in: | Science (American Association for the Advancement of Science) 1986-10, Vol.234 (4775), p.451-457 |
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creator | Hill, D.E Hope, I.A Macke, J.P Struhl, K |
description | Expression of the yeast his3 and other amino acid biosynthetic genes is induced during conditions of amino acid starvation. The coordination of this response is mediated by a positive regulatory protein called GCN4, which binds specifically to regulatory sites upstream of all coregulated genes and stimulates their transcription. The nucleotide sequence requirements of the his3 regulatory site were determined by analysis of numerous point mutations obtained by a novel method of cloning oligonucleotides. Almost all single base pair mutations within the nine base pair sequence ATGACTCTT significantly reduce his3 induction in vivo and GCN4 binding in vitro, whereas changes outside this region have minimal effects. One mutation, which generates a sequence that most closely resembles the consensus for 15 coregulated genes, increases both the level of induction and the affinity for GCN4 protein. The palindromic nature of the optimal sequence, ATGACTCAT, suggests that GCN4 protein binds as a dimer to adjacent half-sites that possibly overlap. |
doi_str_mv | 10.1126/science.3532321 |
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The coordination of this response is mediated by a positive regulatory protein called GCN4, which binds specifically to regulatory sites upstream of all coregulated genes and stimulates their transcription. The nucleotide sequence requirements of the his3 regulatory site were determined by analysis of numerous point mutations obtained by a novel method of cloning oligonucleotides. Almost all single base pair mutations within the nine base pair sequence ATGACTCTT significantly reduce his3 induction in vivo and GCN4 binding in vitro, whereas changes outside this region have minimal effects. One mutation, which generates a sequence that most closely resembles the consensus for 15 coregulated genes, increases both the level of induction and the affinity for GCN4 protein. The palindromic nature of the optimal sequence, ATGACTCAT, suggests that GCN4 protein binds as a dimer to adjacent half-sites that possibly overlap.</description><identifier>ISSN: 0036-8075</identifier><identifier>EISSN: 1095-9203</identifier><identifier>DOI: 10.1126/science.3532321</identifier><identifier>PMID: 3532321</identifier><identifier>CODEN: SCIEAS</identifier><language>eng</language><publisher>United States: The American Association for the Advancement of Science</publisher><subject>Acids ; ADN ; Alleles ; Base Sequence ; Biochemistry ; DNA ; DNA, Fungal - genetics ; DNA-Binding Proteins ; Enzyme Induction ; Fungal Proteins - physiology ; GENE ; Gene expression ; GENES ; Genes, Regulator ; Genetic mutation ; Genetic regulation ; Genetic transcription ; Genetics ; Histidine - genetics ; MUTACION ; Mutagenesis ; MUTATION ; Nucleotide sequences ; Nucleotides ; Oligonucleotides ; Point mutation ; Promoter regions ; Protein Kinases ; PROTEINAS ; PROTEINE ; PROTEINS ; RNA ; SACCHAROMYCES CEREVISIAE ; Saccharomyces cerevisiae - genetics ; Saccharomyces cerevisiae Proteins ; Sequence Homology, Nucleic Acid ; Transcription (Genetics) ; Transcription Factors - physiology ; Transcription, Genetic</subject><ispartof>Science (American Association for the Advancement of Science), 1986-10, Vol.234 (4775), p.451-457</ispartof><rights>Copyright 1986 The American Association for the Advancement of Science</rights><rights>COPYRIGHT 1986 American Association for the Advancement of Science</rights><rights>COPYRIGHT 1986 American Association for the Advancement of Science</rights><rights>Copyright American Association for the Advancement of Science Oct 24, 1986</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c651t-60e5738885a0bd80f7859051cd8e0c6269bee3aac683db99e8bcd795dd9bc6a53</citedby><cites>FETCH-LOGICAL-c651t-60e5738885a0bd80f7859051cd8e0c6269bee3aac683db99e8bcd795dd9bc6a53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/1697341$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/1697341$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,803,2884,2885,27924,27925,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3532321$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hill, D.E</creatorcontrib><creatorcontrib>Hope, I.A</creatorcontrib><creatorcontrib>Macke, J.P</creatorcontrib><creatorcontrib>Struhl, K</creatorcontrib><title>Saturation mutagenesis of the yeast his3 regulatory site: requirements for transcriptional induction and for binding by GCN4 activator protein</title><title>Science (American Association for the Advancement of Science)</title><addtitle>Science</addtitle><description>Expression of the yeast his3 and other amino acid biosynthetic genes is induced during conditions of amino acid starvation. The coordination of this response is mediated by a positive regulatory protein called GCN4, which binds specifically to regulatory sites upstream of all coregulated genes and stimulates their transcription. The nucleotide sequence requirements of the his3 regulatory site were determined by analysis of numerous point mutations obtained by a novel method of cloning oligonucleotides. Almost all single base pair mutations within the nine base pair sequence ATGACTCTT significantly reduce his3 induction in vivo and GCN4 binding in vitro, whereas changes outside this region have minimal effects. One mutation, which generates a sequence that most closely resembles the consensus for 15 coregulated genes, increases both the level of induction and the affinity for GCN4 protein. The palindromic nature of the optimal sequence, ATGACTCAT, suggests that GCN4 protein binds as a dimer to adjacent half-sites that possibly overlap.</description><subject>Acids</subject><subject>ADN</subject><subject>Alleles</subject><subject>Base Sequence</subject><subject>Biochemistry</subject><subject>DNA</subject><subject>DNA, Fungal - genetics</subject><subject>DNA-Binding Proteins</subject><subject>Enzyme Induction</subject><subject>Fungal Proteins - physiology</subject><subject>GENE</subject><subject>Gene expression</subject><subject>GENES</subject><subject>Genes, Regulator</subject><subject>Genetic mutation</subject><subject>Genetic regulation</subject><subject>Genetic transcription</subject><subject>Genetics</subject><subject>Histidine - genetics</subject><subject>MUTACION</subject><subject>Mutagenesis</subject><subject>MUTATION</subject><subject>Nucleotide sequences</subject><subject>Nucleotides</subject><subject>Oligonucleotides</subject><subject>Point mutation</subject><subject>Promoter regions</subject><subject>Protein Kinases</subject><subject>PROTEINAS</subject><subject>PROTEINE</subject><subject>PROTEINS</subject><subject>RNA</subject><subject>SACCHAROMYCES CEREVISIAE</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Saccharomyces cerevisiae Proteins</subject><subject>Sequence Homology, Nucleic Acid</subject><subject>Transcription (Genetics)</subject><subject>Transcription Factors - physiology</subject><subject>Transcription, Genetic</subject><issn>0036-8075</issn><issn>1095-9203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN00Fv0zAUB_AIgcYonJEQSBYHOIxudhwn9m6jgjKpWg9lXC3HeclcpXFnO4h-CT4zzlqxgSqtyiHSe7_8rdjPSfKa4FNC0vzMawOdhlPKaEpT8iQ5JliwsUgxfZocY0zzMccFe5688H6JcewJepQc7fhx8nuhQu9UMLZDqz6oBjrwxiNbo3ADaAPKB3RjPEUOmr5VwboN8ibAeSzc9sbBCrrgUW0dCk51XjuzHtJUi0xX9fouWXXVnShjyXQNKjdoOrnKkIrtn0MmWjsbwHQvk2e1aj282r1HyfXXL98n38az-fRycjEb65yRMM4xsIJyzpnCZcVxXXAmMCO64oB1nuaiBKBK6ZzTqhQCeKmrQrCqEqXOFaOj5MM2N65724MPcmW8hrZVHdjeSxozcF48DlNCKGaZeBSSLM-YEDjC9__Bpe1d3K8hjLI0LzCJ6GSLGtWCNF1t4-bq4XCcam0HtYnli4wRnsZfHCWf9uj4VLAyeg__-A-PIsCv0Kjee3m5uDpUzn8cKj9PD5R8OnsoT_ZJbdsWGpBxICbzh_psq7Wz3juo5dqZlXIbSbAc7orc3RW5G_74xbvdSfTlCqq__r7_dttf-jii93G5KGg2tN9s27WyUjXOeHm94AUWvCD0D30lIJQ</recordid><startdate>19861024</startdate><enddate>19861024</enddate><creator>Hill, D.E</creator><creator>Hope, I.A</creator><creator>Macke, J.P</creator><creator>Struhl, K</creator><general>The American Association for the Advancement of Science</general><general>American Association for the Advancement of Science</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>8GL</scope><scope>IBG</scope><scope>IOV</scope><scope>ISN</scope><scope>7QF</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QQ</scope><scope>7QR</scope><scope>7SC</scope><scope>7SE</scope><scope>7SN</scope><scope>7SP</scope><scope>7SR</scope><scope>7SS</scope><scope>7T7</scope><scope>7TA</scope><scope>7TB</scope><scope>7TK</scope><scope>7TM</scope><scope>7U5</scope><scope>7U9</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>H94</scope><scope>JG9</scope><scope>JQ2</scope><scope>K9.</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>19861024</creationdate><title>Saturation mutagenesis of the yeast his3 regulatory site: requirements for transcriptional induction and for binding by GCN4 activator protein</title><author>Hill, D.E ; Hope, I.A ; Macke, J.P ; Struhl, K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c651t-60e5738885a0bd80f7859051cd8e0c6269bee3aac683db99e8bcd795dd9bc6a53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><topic>Acids</topic><topic>ADN</topic><topic>Alleles</topic><topic>Base Sequence</topic><topic>Biochemistry</topic><topic>DNA</topic><topic>DNA, Fungal - genetics</topic><topic>DNA-Binding Proteins</topic><topic>Enzyme Induction</topic><topic>Fungal Proteins - physiology</topic><topic>GENE</topic><topic>Gene expression</topic><topic>GENES</topic><topic>Genes, Regulator</topic><topic>Genetic mutation</topic><topic>Genetic regulation</topic><topic>Genetic transcription</topic><topic>Genetics</topic><topic>Histidine - genetics</topic><topic>MUTACION</topic><topic>Mutagenesis</topic><topic>MUTATION</topic><topic>Nucleotide sequences</topic><topic>Nucleotides</topic><topic>Oligonucleotides</topic><topic>Point mutation</topic><topic>Promoter regions</topic><topic>Protein Kinases</topic><topic>PROTEINAS</topic><topic>PROTEINE</topic><topic>PROTEINS</topic><topic>RNA</topic><topic>SACCHAROMYCES CEREVISIAE</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Saccharomyces cerevisiae Proteins</topic><topic>Sequence Homology, Nucleic Acid</topic><topic>Transcription (Genetics)</topic><topic>Transcription Factors - physiology</topic><topic>Transcription, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hill, D.E</creatorcontrib><creatorcontrib>Hope, I.A</creatorcontrib><creatorcontrib>Macke, J.P</creatorcontrib><creatorcontrib>Struhl, K</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: High School</collection><collection>Gale In Context: Biography</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Canada</collection><collection>Aluminium Industry Abstracts</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Ecology Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Science (American Association for the Advancement of Science)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hill, D.E</au><au>Hope, I.A</au><au>Macke, J.P</au><au>Struhl, K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Saturation mutagenesis of the yeast his3 regulatory site: requirements for transcriptional induction and for binding by GCN4 activator protein</atitle><jtitle>Science (American Association for the Advancement of Science)</jtitle><addtitle>Science</addtitle><date>1986-10-24</date><risdate>1986</risdate><volume>234</volume><issue>4775</issue><spage>451</spage><epage>457</epage><pages>451-457</pages><issn>0036-8075</issn><eissn>1095-9203</eissn><coden>SCIEAS</coden><abstract>Expression of the yeast his3 and other amino acid biosynthetic genes is induced during conditions of amino acid starvation. The coordination of this response is mediated by a positive regulatory protein called GCN4, which binds specifically to regulatory sites upstream of all coregulated genes and stimulates their transcription. The nucleotide sequence requirements of the his3 regulatory site were determined by analysis of numerous point mutations obtained by a novel method of cloning oligonucleotides. Almost all single base pair mutations within the nine base pair sequence ATGACTCTT significantly reduce his3 induction in vivo and GCN4 binding in vitro, whereas changes outside this region have minimal effects. One mutation, which generates a sequence that most closely resembles the consensus for 15 coregulated genes, increases both the level of induction and the affinity for GCN4 protein. The palindromic nature of the optimal sequence, ATGACTCAT, suggests that GCN4 protein binds as a dimer to adjacent half-sites that possibly overlap.</abstract><cop>United States</cop><pub>The American Association for the Advancement of Science</pub><pmid>3532321</pmid><doi>10.1126/science.3532321</doi><tpages>7</tpages></addata></record> |
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subjects | Acids ADN Alleles Base Sequence Biochemistry DNA DNA, Fungal - genetics DNA-Binding Proteins Enzyme Induction Fungal Proteins - physiology GENE Gene expression GENES Genes, Regulator Genetic mutation Genetic regulation Genetic transcription Genetics Histidine - genetics MUTACION Mutagenesis MUTATION Nucleotide sequences Nucleotides Oligonucleotides Point mutation Promoter regions Protein Kinases PROTEINAS PROTEINE PROTEINS RNA SACCHAROMYCES CEREVISIAE Saccharomyces cerevisiae - genetics Saccharomyces cerevisiae Proteins Sequence Homology, Nucleic Acid Transcription (Genetics) Transcription Factors - physiology Transcription, Genetic |
title | Saturation mutagenesis of the yeast his3 regulatory site: requirements for transcriptional induction and for binding by GCN4 activator protein |
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