The Type of Basal Promoter Determines the Regulated or Constitutive Mode of Transcription in the Common Control Region of the Yeast Gene Pair GCY1/RIO1
The yeast genes, GCY1 andRIO1, are transcribed divergently from the 869-base pair intergenic region. GCY1 is inducible by galactose about 25-fold due to Gal4p-binding to a singleUASGAL, whereas RIO1 is constitutively expressed. GCY1 has a TATA box obeying the consensus TATAAA, whereas the RIO1 5′-up...
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Published in | The Journal of biological chemistry Vol. 272; no. 50; pp. 31630 - 31635 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
12.12.1997
American Society for Biochemistry and Molecular Biology |
Subjects | |
Online Access | Get full text |
ISSN | 0021-9258 1083-351X |
DOI | 10.1074/jbc.272.50.31630 |
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Abstract | The yeast genes, GCY1 andRIO1, are transcribed divergently from the 869-base pair intergenic region. GCY1 is inducible by galactose about 25-fold due to Gal4p-binding to a singleUASGAL, whereas RIO1 is constitutively expressed. GCY1 has a TATA box obeying the consensus TATAAA, whereas the RIO1 5′-upstream region lacks such a motif. In vitro mutagenesis of the TATA motif ofGCY1, on the one hand, and introduction of a TATA-element into the promoter of RIO1, on the other hand, as well as inversion of the intergenic region have revealed that transcription ofGCY1 and RIO1 is only regulated by Gal4p when a consensus TATA motif is included in their core promoters but not in its absence. The data imply that only transcription complexes that assemble at a consensus TATA box are compatible with specific transactivators, such as Gal4p. As a result, the adjacent gene is subject to regulated expression. By contrast, if a consensus TATA sequence is absent, the initiation complex does not respond to regulatory transcription factors, and consequently, the respective gene is constitutively transcribed. On the other hand, we show that two blocks of homo-oligomeric (dA·dT) sequences do not function as boundary sequences that might confine regulatory action of Gal4p toGCY1. |
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AbstractList | The yeast genes, GCY1 and RIO1, are transcribed divergently from the 869-base pair intergenic region. GCY1 is inducible by galactose about 25-fold due to Gal4p-binding to a single UAS sub(GAL), whereas RIO1 is constitutively expressed. GCY1 has a TATA box obeying the consensus TATAAA, whereas the RIO1 5'-upstream region lacks such a motif. In vitro mutagenesis of the TATA motif of GCY1, on the one hand, and introduction of a TATA-element into the promoter of RIO1, on the other hand, as well as inversion of the intergenic region have revealed that transcription of GCY1 and RIO1 is only regulated by Gal4p when a consensus TATA motif is included in their core promoters but not in its absence. The data imply that only transcription complexes that assemble at a consensus TATA box are compatible with specific transactivators, such as Gal4p. As a result, the adjacent gene is subject to regulated expression. By contrast, if a consensus TATA sequence is absent, the initiation complex does not respond to regulatory transcription factors, and consequently, the respective gene is constitutively transcribed. On the other hand, we show that two blocks of homo-oligomeric (dA-dT) sequences do not function as boundary sequences that might confine regulatory action of Gal4p to GCY1. The yeast genes, GCY1 and RIO1 , are transcribed divergently from the 869-base pair intergenic region. GCY1 is inducible by galactose about 25-fold due to Gal4p-binding to a single UAS GAL , whereas RIO1 is constitutively expressed. GCY1 has a TATA box obeying the consensus TATAAA, whereas the RIO1 5â²-upstream region lacks such a motif. In vitro mutagenesis of the TATA motif of GCY1 , on the one hand, and introduction of a TATA-element into the promoter of RIO1 , on the other hand, as well as inversion of the intergenic region have revealed that transcription of GCY1 and RIO1 is only regulated by Gal4p when a consensus TATA motif is included in their core promoters but not in its absence. The data imply that only transcription complexes that assemble at a consensus TATA box are compatible with specific transactivators, such as Gal4p. As a result, the adjacent gene is subject to regulated expression. By contrast, if a consensus TATA sequence is absent, the initiation complex does not respond to regulatory transcription factors, and consequently, the respective gene is constitutively transcribed. On the other hand, we show that two blocks of homo-oligomeric (dA·dT) sequences do not function as boundary sequences that might confine regulatory action of Gal4p to GCY1 . The yeast genes, GCY1 and RIO1, are transcribed divergently from the 869-base pair intergenic region. GCY1 is inducible by galactose about 25-fold due to Gal4p-binding to a single UASGAL, whereas RIO1 is constitutively expressed. GCY1 has a TATA box obeying the consensus TATAAA, whereas the RIO1 5'-upstream region lacks such a motif. In vitro mutagenesis of the TATA motif of GCY1, on the one hand, and introduction of a TATA-element into the promoter of RIO1, on the other hand, as well as inversion of the intergenic region have revealed that transcription of GCY1 and RIO1 is only regulated by Gal4p when a consensus TATA motif is included in their core promoters but not in its absence. The data imply that only transcription complexes that assemble at a consensus TATA box are compatible with specific transactivators, such as Gal4p. As a result, the adjacent gene is subject to regulated expression. By contrast, if a consensus TATA sequence is absent, the initiation complex does not respond to regulatory transcription factors, and consequently, the respective gene is constitutively transcribed. On the other hand, we show that two blocks of homo-oligomeric (dA.dT) sequences do not function as boundary sequences that might confine regulatory action of Gal4p to GCY1. The yeast genes, GCY1 and RIO1, are transcribed divergently from the 869-base pair intergenic region. GCY1 is inducible by galactose about 25-fold due to Gal4p-binding to a single UASGAL, whereas RIO1 is constitutively expressed. GCY1 has a TATA box obeying the consensus TATAAA, whereas the RIO1 5'-upstream region lacks such a motif. In vitro mutagenesis of the TATA motif of GCY1, on the one hand, and introduction of a TATA-element into the promoter of RIO1, on the other hand, as well as inversion of the intergenic region have revealed that transcription of GCY1 and RIO1 is only regulated by Gal4p when a consensus TATA motif is included in their core promoters but not in its absence. The data imply that only transcription complexes that assemble at a consensus TATA box are compatible with specific transactivators, such as Gal4p. As a result, the adjacent gene is subject to regulated expression. By contrast, if a consensus TATA sequence is absent, the initiation complex does not respond to regulatory transcription factors, and consequently, the respective gene is constitutively transcribed. On the other hand, we show that two blocks of homo-oligomeric (dA.dT) sequences do not function as boundary sequences that might confine regulatory action of Gal4p to GCY1.The yeast genes, GCY1 and RIO1, are transcribed divergently from the 869-base pair intergenic region. GCY1 is inducible by galactose about 25-fold due to Gal4p-binding to a single UASGAL, whereas RIO1 is constitutively expressed. GCY1 has a TATA box obeying the consensus TATAAA, whereas the RIO1 5'-upstream region lacks such a motif. In vitro mutagenesis of the TATA motif of GCY1, on the one hand, and introduction of a TATA-element into the promoter of RIO1, on the other hand, as well as inversion of the intergenic region have revealed that transcription of GCY1 and RIO1 is only regulated by Gal4p when a consensus TATA motif is included in their core promoters but not in its absence. The data imply that only transcription complexes that assemble at a consensus TATA box are compatible with specific transactivators, such as Gal4p. As a result, the adjacent gene is subject to regulated expression. By contrast, if a consensus TATA sequence is absent, the initiation complex does not respond to regulatory transcription factors, and consequently, the respective gene is constitutively transcribed. On the other hand, we show that two blocks of homo-oligomeric (dA.dT) sequences do not function as boundary sequences that might confine regulatory action of Gal4p to GCY1. The yeast genes, GCY1 andRIO1, are transcribed divergently from the 869-base pair intergenic region. GCY1 is inducible by galactose about 25-fold due to Gal4p-binding to a singleUASGAL, whereas RIO1 is constitutively expressed. GCY1 has a TATA box obeying the consensus TATAAA, whereas the RIO1 5′-upstream region lacks such a motif. In vitro mutagenesis of the TATA motif ofGCY1, on the one hand, and introduction of a TATA-element into the promoter of RIO1, on the other hand, as well as inversion of the intergenic region have revealed that transcription ofGCY1 and RIO1 is only regulated by Gal4p when a consensus TATA motif is included in their core promoters but not in its absence. The data imply that only transcription complexes that assemble at a consensus TATA box are compatible with specific transactivators, such as Gal4p. As a result, the adjacent gene is subject to regulated expression. By contrast, if a consensus TATA sequence is absent, the initiation complex does not respond to regulatory transcription factors, and consequently, the respective gene is constitutively transcribed. On the other hand, we show that two blocks of homo-oligomeric (dA·dT) sequences do not function as boundary sequences that might confine regulatory action of Gal4p toGCY1. |
Author | Bandlow, Wolfhard Angermayr, Michaela |
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Snippet | The yeast genes, GCY1 andRIO1, are transcribed divergently from the 869-base pair intergenic region. GCY1 is inducible by galactose about 25-fold due to... The yeast genes, GCY1 and RIO1 , are transcribed divergently from the 869-base pair intergenic region. GCY1 is inducible by galactose about 25-fold due to... The yeast genes, GCY1 and RIO1, are transcribed divergently from the 869-base pair intergenic region. GCY1 is inducible by galactose about 25-fold due to... |
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SubjectTerms | ADN ADN RECOMBINADO ADN RECOMBINE ALDO-KETO REDUCTASE BETA GALACTOSIDASA BETA GALACTOSIDASE BINDING Binding Sites Chromosome Inversion Chromosome Mapping Consensus Sequence CRYSTALLIN LIKE YEAST PROTEIN DNA DNA-Binding Proteins EXPRESION GENICA EXPRESSION DES GENES FACTEUR DE TRANSCRIPTION FACTORES DE TRANSCRIPCION GALACTOSA GALACTOSE Galactose - pharmacology GCY1 GENE GENE GENE EXPRESSION GENES Genes, Fungal GENETIC REGULATION GENETICA GENETICS GENETIQUE GTP-Binding Proteins GTP-Binding Proteins - metabolism INTERGENIC DNA metabolism NUCLEOTIDE SEQUENCE Oligodeoxyribonucleotides Oligodeoxyribonucleotides - metabolism OXIDOREDUCTASES OXIDORREDUCTASAS OXYDOREDUCTASE pharmacology Poly dA-dT Poly dA-dT - metabolism Promoter Regions, Genetic PROTEINAS PROTEINE PROTEINS rap GTP-Binding Proteins RECOMBINANT DNA REPORTER GENES RIO1 GENE SACCHAROMYCES CEREVISIAE Saccharomyces cerevisiae - genetics Saccharomyces cerevisiae Proteins SECUENCIA NUCLEOTIDICA SEQUENCE NUCLEOTIDIQUE TATA BOX TRANSCRIPCION TRANSCRIPTION transcription (genetics) TRANSCRIPTION FACTORS Transcription Factors - metabolism Transcription, Genetic |
Title | The Type of Basal Promoter Determines the Regulated or Constitutive Mode of Transcription in the Common Control Region of the Yeast Gene Pair GCY1/RIO1 |
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