Design of a minimal silencer for the silent mating-type locus HML of Saccharomyces cerevisiae
The silent mating-type loci HML and HMR of Saccharomyces cerevisiae contain mating-type information that is permanently repressed. This silencing is mediated by flanking sequence elements, the E- and I-silencers. They contain combinations of binding sites for the proteins Rap1, Abf1 and Sum1 as well...
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description | The silent mating-type loci HML and HMR of Saccharomyces cerevisiae contain mating-type information that is permanently repressed. This silencing is mediated by flanking sequence elements, the E- and I-silencers. They contain combinations of binding sites for the proteins Rap1, Abf1 and Sum1 as well as for the origin recognition complex (ORC). Together, they recruit other silencing factors, foremost the repressive Sir2/Sir3/Sir4 complex, to establish heterochromatin-like structures at the HM loci. However, the HM silencers exhibit considerable functional redundancy, which has hampered the identification of further silencing factors. In this study, we constructed a synthetic HML-E silencer (HML-SS ΔI) that lacked this redundancy. It consisted solely of Rap1 and ORC-binding sites and the D2 element, a Sum1-binding site. All three elements were crucial for minimal HML silencing, and mutations in these elements led to a loss of Sir3 recruitment. The silencer was sensitive to a mutation in RAP1, rap1-12, but less sensitive to orc mutations or sum1Δ. Moreover, deletions of SIR1 and DOT1 lead to complete derepression of the HML-SS ΔI silencer. This fully functional, minimal HML-E silencer will therefore be useful to identify novel factors involved in HML silencing. |
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This silencing is mediated by flanking sequence elements, the E- and I-silencers. They contain combinations of binding sites for the proteins Rap1, Abf1 and Sum1 as well as for the origin recognition complex (ORC). Together, they recruit other silencing factors, foremost the repressive Sir2/Sir3/Sir4 complex, to establish heterochromatin-like structures at the HM loci. However, the HM silencers exhibit considerable functional redundancy, which has hampered the identification of further silencing factors. In this study, we constructed a synthetic HML-E silencer (HML-SS ΔI) that lacked this redundancy. It consisted solely of Rap1 and ORC-binding sites and the D2 element, a Sum1-binding site. All three elements were crucial for minimal HML silencing, and mutations in these elements led to a loss of Sir3 recruitment. The silencer was sensitive to a mutation in RAP1, rap1-12, but less sensitive to orc mutations or sum1Δ. Moreover, deletions of SIR1 and DOT1 lead to complete derepression of the HML-SS ΔI silencer. This fully functional, minimal HML-E silencer will therefore be useful to identify novel factors involved in HML silencing.</description><identifier>ISSN: 0305-1048</identifier><identifier>ISSN: 1362-4962</identifier><identifier>EISSN: 1362-4962</identifier><identifier>DOI: 10.1093/nar/gkq689</identifier><identifier>PMID: 20699276</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Binding Sites ; Gene Expression Regulation, Fungal ; Gene Regulation, Chromatin and Epigenetics ; Gene Silencing ; Genes, Mating Type, Fungal ; Genetic Loci ; Histone-Lysine N-Methyltransferase - genetics ; Mutation ; Nuclear Proteins - genetics ; Oligonucleotides - chemistry ; Origin Recognition Complex - metabolism ; Saccharomyces cerevisiae ; Saccharomyces cerevisiae - genetics ; Saccharomyces cerevisiae Proteins - genetics ; Saccharomyces cerevisiae Proteins - metabolism ; Silencer Elements, Transcriptional ; Silent Information Regulator Proteins, Saccharomyces cerevisiae - genetics ; Telomere-Binding Proteins - metabolism ; Transcription Factors - metabolism</subject><ispartof>Nucleic acids research, 2010-12, Vol.38 (22), p.7991-8000</ispartof><rights>The Author(s) 2010. Published by Oxford University Press. 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c433t-817f6cc82c82eb5f61fa76efe83ca08246331deba7172ed1cd4d31073ce2290f3</citedby><cites>FETCH-LOGICAL-c433t-817f6cc82c82eb5f61fa76efe83ca08246331deba7172ed1cd4d31073ce2290f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001064/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001064/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,865,886,27928,27929,53795,53797</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20699276$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Weber, Jan M</creatorcontrib><creatorcontrib>Ehrenhofer-Murray, Ann E</creatorcontrib><title>Design of a minimal silencer for the silent mating-type locus HML of Saccharomyces cerevisiae</title><title>Nucleic acids research</title><addtitle>Nucleic Acids Res</addtitle><description>The silent mating-type loci HML and HMR of Saccharomyces cerevisiae contain mating-type information that is permanently repressed. This silencing is mediated by flanking sequence elements, the E- and I-silencers. They contain combinations of binding sites for the proteins Rap1, Abf1 and Sum1 as well as for the origin recognition complex (ORC). Together, they recruit other silencing factors, foremost the repressive Sir2/Sir3/Sir4 complex, to establish heterochromatin-like structures at the HM loci. However, the HM silencers exhibit considerable functional redundancy, which has hampered the identification of further silencing factors. In this study, we constructed a synthetic HML-E silencer (HML-SS ΔI) that lacked this redundancy. It consisted solely of Rap1 and ORC-binding sites and the D2 element, a Sum1-binding site. All three elements were crucial for minimal HML silencing, and mutations in these elements led to a loss of Sir3 recruitment. The silencer was sensitive to a mutation in RAP1, rap1-12, but less sensitive to orc mutations or sum1Δ. Moreover, deletions of SIR1 and DOT1 lead to complete derepression of the HML-SS ΔI silencer. This fully functional, minimal HML-E silencer will therefore be useful to identify novel factors involved in HML silencing.</description><subject>Binding Sites</subject><subject>Gene Expression Regulation, Fungal</subject><subject>Gene Regulation, Chromatin and Epigenetics</subject><subject>Gene Silencing</subject><subject>Genes, Mating Type, Fungal</subject><subject>Genetic Loci</subject><subject>Histone-Lysine N-Methyltransferase - genetics</subject><subject>Mutation</subject><subject>Nuclear Proteins - genetics</subject><subject>Oligonucleotides - chemistry</subject><subject>Origin Recognition Complex - metabolism</subject><subject>Saccharomyces cerevisiae</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Saccharomyces cerevisiae Proteins - genetics</subject><subject>Saccharomyces cerevisiae Proteins - metabolism</subject><subject>Silencer Elements, Transcriptional</subject><subject>Silent Information Regulator Proteins, Saccharomyces cerevisiae - genetics</subject><subject>Telomere-Binding Proteins - metabolism</subject><subject>Transcription Factors - metabolism</subject><issn>0305-1048</issn><issn>1362-4962</issn><issn>1362-4962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1r3DAQhkVpaLZpL_0BrW6FghuNJMvypRDSjxQ25JDmWIRWHnnV2tZG8gb231fBaWhPgYGBmWdeZuYl5A2wj8BacTrZdNr_vlW6fUZWIBSvZKv4c7JigtUVMKmPycucfzEGEmr5ghxzptqWN2pFfn7GHPqJRk8tHcMURjvQHAacHCbqY6LzFpfCTEc7h6mv5sMO6RDdPtOLy_X96LV1bmtTHA8OMy2TeBdysPiKHHk7ZHz9kE_IzdcvP84vqvXVt-_nZ-vKSSHmSkPjlXOal8BN7RV42yj0qIWzTHOphIAON7aBhmMHrpOdANYIh5y3zIsT8mnR3e03I3auLJvsYHapnJMOJtpg_u9MYWv6eGdE-QlTsgi8fxBI8XaPeTZjyA6HwU4Y99noWshGgW6eJkFLJmqtC_lhIV2KOSf0j_sAM_fGmWKcWYwr8Nt_L3hE_zpVgHcL4G00tk8hm5trzkAwaIWoAcQfMTuflQ</recordid><startdate>20101201</startdate><enddate>20101201</enddate><creator>Weber, Jan M</creator><creator>Ehrenhofer-Murray, Ann E</creator><general>Oxford University Press</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>7X8</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>20101201</creationdate><title>Design of a minimal silencer for the silent mating-type locus HML of Saccharomyces cerevisiae</title><author>Weber, Jan M ; Ehrenhofer-Murray, Ann E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c433t-817f6cc82c82eb5f61fa76efe83ca08246331deba7172ed1cd4d31073ce2290f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Binding Sites</topic><topic>Gene Expression Regulation, Fungal</topic><topic>Gene Regulation, Chromatin and Epigenetics</topic><topic>Gene Silencing</topic><topic>Genes, Mating Type, Fungal</topic><topic>Genetic Loci</topic><topic>Histone-Lysine N-Methyltransferase - genetics</topic><topic>Mutation</topic><topic>Nuclear Proteins - genetics</topic><topic>Oligonucleotides - chemistry</topic><topic>Origin Recognition Complex - metabolism</topic><topic>Saccharomyces cerevisiae</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Saccharomyces cerevisiae Proteins - genetics</topic><topic>Saccharomyces cerevisiae Proteins - metabolism</topic><topic>Silencer Elements, Transcriptional</topic><topic>Silent Information Regulator Proteins, Saccharomyces cerevisiae - genetics</topic><topic>Telomere-Binding Proteins - metabolism</topic><topic>Transcription Factors - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Weber, Jan M</creatorcontrib><creatorcontrib>Ehrenhofer-Murray, Ann E</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>MEDLINE - Academic</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nucleic acids research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Weber, Jan M</au><au>Ehrenhofer-Murray, Ann E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Design of a minimal silencer for the silent mating-type locus HML of Saccharomyces cerevisiae</atitle><jtitle>Nucleic acids research</jtitle><addtitle>Nucleic Acids Res</addtitle><date>2010-12-01</date><risdate>2010</risdate><volume>38</volume><issue>22</issue><spage>7991</spage><epage>8000</epage><pages>7991-8000</pages><issn>0305-1048</issn><issn>1362-4962</issn><eissn>1362-4962</eissn><abstract>The silent mating-type loci HML and HMR of Saccharomyces cerevisiae contain mating-type information that is permanently repressed. This silencing is mediated by flanking sequence elements, the E- and I-silencers. They contain combinations of binding sites for the proteins Rap1, Abf1 and Sum1 as well as for the origin recognition complex (ORC). Together, they recruit other silencing factors, foremost the repressive Sir2/Sir3/Sir4 complex, to establish heterochromatin-like structures at the HM loci. However, the HM silencers exhibit considerable functional redundancy, which has hampered the identification of further silencing factors. In this study, we constructed a synthetic HML-E silencer (HML-SS ΔI) that lacked this redundancy. It consisted solely of Rap1 and ORC-binding sites and the D2 element, a Sum1-binding site. All three elements were crucial for minimal HML silencing, and mutations in these elements led to a loss of Sir3 recruitment. The silencer was sensitive to a mutation in RAP1, rap1-12, but less sensitive to orc mutations or sum1Δ. Moreover, deletions of SIR1 and DOT1 lead to complete derepression of the HML-SS ΔI silencer. This fully functional, minimal HML-E silencer will therefore be useful to identify novel factors involved in HML silencing.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>20699276</pmid><doi>10.1093/nar/gkq689</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Binding Sites Gene Expression Regulation, Fungal Gene Regulation, Chromatin and Epigenetics Gene Silencing Genes, Mating Type, Fungal Genetic Loci Histone-Lysine N-Methyltransferase - genetics Mutation Nuclear Proteins - genetics Oligonucleotides - chemistry Origin Recognition Complex - metabolism Saccharomyces cerevisiae Saccharomyces cerevisiae - genetics Saccharomyces cerevisiae Proteins - genetics Saccharomyces cerevisiae Proteins - metabolism Silencer Elements, Transcriptional Silent Information Regulator Proteins, Saccharomyces cerevisiae - genetics Telomere-Binding Proteins - metabolism Transcription Factors - metabolism |
title | Design of a minimal silencer for the silent mating-type locus HML of Saccharomyces cerevisiae |
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