Yeast Frameshift Suppressor Mutations in the Genes Coding for Transcription Factor Mbf1p and Ribosomal Protein S3: Evidence for Autoregulation of S3 Synthesis
The SUF13 and SUF14 genes were identified among extragenic suppressors of +1 frameshift mutations. SUF13 is synonymous with MBF1, a single-copy nonessential gene coding for a POLII transcription factor. The suf13-1 mutation is a two-nucleotide deletion in the SUF13/MBF1 coding region. A suf13::TRP1...
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Veröffentlicht in: | Genetics (Austin) 2001-03, Vol.157 (3), p.1141-1158 |
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description | The SUF13 and SUF14 genes were identified among extragenic suppressors of +1 frameshift mutations. SUF13 is synonymous with MBF1, a single-copy nonessential gene coding for a POLII transcription factor. The suf13-1 mutation is a two-nucleotide deletion in the SUF13/MBF1 coding region. A suf13::TRP1 null mutant suppresses +1 frameshift mutations, indicating that suppression is caused by loss of SUF13 function. The suf13-1 suppressor alters sensitivity to aminoglycoside antibiotics and reduces the accumulation of his4-713 mRNA, suggesting that suppression is mediated at the translational level. The SUF14 gene is synonymous with RPS3, a single-copy essential gene that codes for the ribosomal protein S3. The suf14-1 mutation is a missense substitution in the coding region. Increased expression of S3 limits the accumulation of SUF14 mRNA, suggesting that expression is autoregulated. A frameshift mutation in SUF14 that prevents full-length translation eliminated regulation, indicating that S3 is required for regulation. Using CUP1-SUF14 and SUF14-lacZ fusions, run-on transcription assays, and estimates of mRNA half-life, our results show that transcription plays a minor role if any in regulation and that the 5'-UTR is necessary but not sufficient for regulation. A change in mRNA decay rate may be the primary mechanism for regulation. |
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SUF13 is synonymous with MBF1, a single-copy nonessential gene coding for a POLII transcription factor. The suf13-1 mutation is a two-nucleotide deletion in the SUF13/MBF1 coding region. A suf13::TRP1 null mutant suppresses +1 frameshift mutations, indicating that suppression is caused by loss of SUF13 function. The suf13-1 suppressor alters sensitivity to aminoglycoside antibiotics and reduces the accumulation of his4-713 mRNA, suggesting that suppression is mediated at the translational level. The SUF14 gene is synonymous with RPS3, a single-copy essential gene that codes for the ribosomal protein S3. The suf14-1 mutation is a missense substitution in the coding region. Increased expression of S3 limits the accumulation of SUF14 mRNA, suggesting that expression is autoregulated. A frameshift mutation in SUF14 that prevents full-length translation eliminated regulation, indicating that S3 is required for regulation. Using CUP1-SUF14 and SUF14-lacZ fusions, run-on transcription assays, and estimates of mRNA half-life, our results show that transcription plays a minor role if any in regulation and that the 5'-UTR is necessary but not sufficient for regulation. A change in mRNA decay rate may be the primary mechanism for regulation.</description><identifier>ISSN: 0016-6731</identifier><identifier>ISSN: 1943-2631</identifier><identifier>EISSN: 1943-2631</identifier><identifier>DOI: 10.1093/genetics/157.3.1141</identifier><identifier>PMID: 11238400</identifier><identifier>CODEN: GENTAE</identifier><language>eng</language><publisher>United States: Genetics Soc America</publisher><subject>5' Untranslated Regions ; Alleles ; Copper - pharmacology ; Databases, Factual ; Dose-Response Relationship, Drug ; Frameshift Mutation ; Gene Dosage ; Genes ; Genes, Fungal ; Genetics ; Models, Genetic ; Mutation ; Phenotype ; Plasmids - genetics ; Plasmids - metabolism ; Promoter Regions, Genetic ; Ribosomal Proteins - biosynthesis ; Ribosomal Proteins - genetics ; RNA, Messenger - metabolism ; Saccharomyces cerevisiae Proteins ; Suppression, Genetic ; Time Factors ; Trans-Activators - genetics ; Transcription Factors ; Transcription, Genetic ; Transformation, Genetic ; Yeast</subject><ispartof>Genetics (Austin), 2001-03, Vol.157 (3), p.1141-1158</ispartof><rights>Copyright Genetics Society of America Mar 2001</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-c18342589e6c0e2ff70a5a9d8efc591fe5b4e9b3a1d0938894367c0cf4357a23</citedby><cites>FETCH-LOGICAL-c526t-c18342589e6c0e2ff70a5a9d8efc591fe5b4e9b3a1d0938894367c0cf4357a23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11238400$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hendrick, James L</creatorcontrib><creatorcontrib>Wilson, Patricia G</creatorcontrib><creatorcontrib>Edelman, Irving I</creatorcontrib><creatorcontrib>Sandbaken, Mark G</creatorcontrib><creatorcontrib>Ursic, Doris</creatorcontrib><creatorcontrib>Culbertson, Michael R</creatorcontrib><title>Yeast Frameshift Suppressor Mutations in the Genes Coding for Transcription Factor Mbf1p and Ribosomal Protein S3: Evidence for Autoregulation of S3 Synthesis</title><title>Genetics (Austin)</title><addtitle>Genetics</addtitle><description>The SUF13 and SUF14 genes were identified among extragenic suppressors of +1 frameshift mutations. SUF13 is synonymous with MBF1, a single-copy nonessential gene coding for a POLII transcription factor. The suf13-1 mutation is a two-nucleotide deletion in the SUF13/MBF1 coding region. A suf13::TRP1 null mutant suppresses +1 frameshift mutations, indicating that suppression is caused by loss of SUF13 function. The suf13-1 suppressor alters sensitivity to aminoglycoside antibiotics and reduces the accumulation of his4-713 mRNA, suggesting that suppression is mediated at the translational level. The SUF14 gene is synonymous with RPS3, a single-copy essential gene that codes for the ribosomal protein S3. The suf14-1 mutation is a missense substitution in the coding region. Increased expression of S3 limits the accumulation of SUF14 mRNA, suggesting that expression is autoregulated. A frameshift mutation in SUF14 that prevents full-length translation eliminated regulation, indicating that S3 is required for regulation. Using CUP1-SUF14 and SUF14-lacZ fusions, run-on transcription assays, and estimates of mRNA half-life, our results show that transcription plays a minor role if any in regulation and that the 5'-UTR is necessary but not sufficient for regulation. A change in mRNA decay rate may be the primary mechanism for regulation.</description><subject>5' Untranslated Regions</subject><subject>Alleles</subject><subject>Copper - pharmacology</subject><subject>Databases, Factual</subject><subject>Dose-Response Relationship, Drug</subject><subject>Frameshift Mutation</subject><subject>Gene Dosage</subject><subject>Genes</subject><subject>Genes, Fungal</subject><subject>Genetics</subject><subject>Models, Genetic</subject><subject>Mutation</subject><subject>Phenotype</subject><subject>Plasmids - genetics</subject><subject>Plasmids - metabolism</subject><subject>Promoter Regions, Genetic</subject><subject>Ribosomal Proteins - biosynthesis</subject><subject>Ribosomal Proteins - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Saccharomyces cerevisiae Proteins</subject><subject>Suppression, Genetic</subject><subject>Time Factors</subject><subject>Trans-Activators - genetics</subject><subject>Transcription Factors</subject><subject>Transcription, Genetic</subject><subject>Transformation, Genetic</subject><subject>Yeast</subject><issn>0016-6731</issn><issn>1943-2631</issn><issn>1943-2631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkc9u1DAYxC0EokvhCZCQxaWnbO04zh8OSNWqW5CKQOxeOFmO8zlxlbWD7XTVl-FZ8XYXKCcf_JuZTzMIvaVkSUnDLnuwEI0Kl5RXS7aktKDP0II2BcvyktHnaEEILbOyYvQMvQrhjhBSNrx-ic4ozVldELJAv36ADBGvvdxBGIyOeDNPk4cQnMdf5iijcTZgY3EcAN-kyIBXrjO2xzoRWy9tUN5MBwyvpYoHWavphKXt8HfTuuB2csTfvIuQXDbsA76-Nx1YBY8OV3OSQD-Pj0nY6YTgzYNNccGE1-iFlmOAN6f3HG3X19vVp-z2683n1dVtpnhexkzRmhU5rxsoFYFc64pILpuuBq14QzXwtoCmZZJ2qbm6Th2VlSJKF4xXMmfn6OPRdprbHXQKbPRyFJM3O-kfhJNG_P9jzSB6dy9oUVJekmTw_mTg3c8ZQhR3bvY2nSzytEte8ooliB0h5V0IHvTfAErEYVLxZ1KRJhVMHCZNqndPb_unOW2YgIsjMJh-2BsPIqTGx4RTsd_vn1j9Bri7r_w</recordid><startdate>20010301</startdate><enddate>20010301</enddate><creator>Hendrick, James L</creator><creator>Wilson, Patricia G</creator><creator>Edelman, Irving I</creator><creator>Sandbaken, Mark G</creator><creator>Ursic, Doris</creator><creator>Culbertson, Michael R</creator><general>Genetics Soc America</general><general>Genetics Society of America</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>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>5PM</scope></search><sort><creationdate>20010301</creationdate><title>Yeast Frameshift Suppressor Mutations in the Genes Coding for Transcription Factor Mbf1p and Ribosomal Protein S3: Evidence for Autoregulation of S3 Synthesis</title><author>Hendrick, James L ; Wilson, Patricia G ; Edelman, Irving I ; Sandbaken, Mark G ; Ursic, Doris ; Culbertson, Michael R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c526t-c18342589e6c0e2ff70a5a9d8efc591fe5b4e9b3a1d0938894367c0cf4357a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>5' Untranslated Regions</topic><topic>Alleles</topic><topic>Copper - pharmacology</topic><topic>Databases, Factual</topic><topic>Dose-Response Relationship, Drug</topic><topic>Frameshift Mutation</topic><topic>Gene Dosage</topic><topic>Genes</topic><topic>Genes, Fungal</topic><topic>Genetics</topic><topic>Models, Genetic</topic><topic>Mutation</topic><topic>Phenotype</topic><topic>Plasmids - genetics</topic><topic>Plasmids - metabolism</topic><topic>Promoter Regions, Genetic</topic><topic>Ribosomal Proteins - biosynthesis</topic><topic>Ribosomal Proteins - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Saccharomyces cerevisiae Proteins</topic><topic>Suppression, Genetic</topic><topic>Time Factors</topic><topic>Trans-Activators - genetics</topic><topic>Transcription Factors</topic><topic>Transcription, Genetic</topic><topic>Transformation, Genetic</topic><topic>Yeast</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hendrick, James L</creatorcontrib><creatorcontrib>Wilson, Patricia G</creatorcontrib><creatorcontrib>Edelman, Irving I</creatorcontrib><creatorcontrib>Sandbaken, Mark G</creatorcontrib><creatorcontrib>Ursic, Doris</creatorcontrib><creatorcontrib>Culbertson, Michael R</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Docstoc</collection><collection>University Readers</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</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>Genetics (Austin)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hendrick, James L</au><au>Wilson, Patricia G</au><au>Edelman, Irving I</au><au>Sandbaken, Mark G</au><au>Ursic, Doris</au><au>Culbertson, Michael R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Yeast Frameshift Suppressor Mutations in the Genes Coding for Transcription Factor Mbf1p and Ribosomal Protein S3: Evidence for Autoregulation of S3 Synthesis</atitle><jtitle>Genetics (Austin)</jtitle><addtitle>Genetics</addtitle><date>2001-03-01</date><risdate>2001</risdate><volume>157</volume><issue>3</issue><spage>1141</spage><epage>1158</epage><pages>1141-1158</pages><issn>0016-6731</issn><issn>1943-2631</issn><eissn>1943-2631</eissn><coden>GENTAE</coden><abstract>The SUF13 and SUF14 genes were identified among extragenic suppressors of +1 frameshift mutations. SUF13 is synonymous with MBF1, a single-copy nonessential gene coding for a POLII transcription factor. The suf13-1 mutation is a two-nucleotide deletion in the SUF13/MBF1 coding region. A suf13::TRP1 null mutant suppresses +1 frameshift mutations, indicating that suppression is caused by loss of SUF13 function. The suf13-1 suppressor alters sensitivity to aminoglycoside antibiotics and reduces the accumulation of his4-713 mRNA, suggesting that suppression is mediated at the translational level. The SUF14 gene is synonymous with RPS3, a single-copy essential gene that codes for the ribosomal protein S3. The suf14-1 mutation is a missense substitution in the coding region. Increased expression of S3 limits the accumulation of SUF14 mRNA, suggesting that expression is autoregulated. A frameshift mutation in SUF14 that prevents full-length translation eliminated regulation, indicating that S3 is required for regulation. Using CUP1-SUF14 and SUF14-lacZ fusions, run-on transcription assays, and estimates of mRNA half-life, our results show that transcription plays a minor role if any in regulation and that the 5'-UTR is necessary but not sufficient for regulation. A change in mRNA decay rate may be the primary mechanism for regulation.</abstract><cop>United States</cop><pub>Genetics Soc America</pub><pmid>11238400</pmid><doi>10.1093/genetics/157.3.1141</doi><tpages>18</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 5' Untranslated Regions Alleles Copper - pharmacology Databases, Factual Dose-Response Relationship, Drug Frameshift Mutation Gene Dosage Genes Genes, Fungal Genetics Models, Genetic Mutation Phenotype Plasmids - genetics Plasmids - metabolism Promoter Regions, Genetic Ribosomal Proteins - biosynthesis Ribosomal Proteins - genetics RNA, Messenger - metabolism Saccharomyces cerevisiae Proteins Suppression, Genetic Time Factors Trans-Activators - genetics Transcription Factors Transcription, Genetic Transformation, Genetic Yeast |
title | Yeast Frameshift Suppressor Mutations in the Genes Coding for Transcription Factor Mbf1p and Ribosomal Protein S3: Evidence for Autoregulation of S3 Synthesis |
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