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 inThe Journal of biological chemistry Vol. 272; no. 50; pp. 31630 - 31635
Main Authors Angermayr, Michaela, Bandlow, Wolfhard
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 12.12.1997
American Society for Biochemistry and Molecular Biology
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ISSN0021-9258
1083-351X
DOI10.1074/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.
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 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 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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StartPage 31630
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
URI https://dx.doi.org/10.1074/jbc.272.50.31630
http://www.jbc.org/content/272/50/31630.abstract
https://www.ncbi.nlm.nih.gov/pubmed/9395503
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https://www.proquest.com/docview/48485453
https://www.proquest.com/docview/79455870
Volume 272
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