Literature DB >> 3279392

The protein factor which binds to the upstream activating sequence of Saccharomyces cerevisiae ENO1 gene.

M Machida1, H Uemura, Y Jigami, H Tanaka.   

Abstract

Using a gel retardation assay it was shown that the 87 bp DNA fragment (UAS87) containing the upstream activating sequence (UAS) of S. cerevisiae EN01 gene and a nuclear extract gave rise to three migration-retarded species specific to UAS87. Heat- or proteinase-treatment of the nuclear extract revealed that these species were protein-DNA complexes. The precise binding region of the protein identified by DNaseI protection analysis was found to include a CCAAACA sequence which forms a dyad-symmetrical structure. The amount of one of the three migration-retarded species significantly increased when cells were grown in medium containing a gluconeogenic carbon source. The introduction of pGCR8, a multicopy plasmid containing GCR1 gene, a regulatory gene controlling the expression of several glycolytic enzymes, showed no effect on the amount of three migration-retarded species.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 3279392      PMCID: PMC336324          DOI: 10.1093/nar/16.4.1407

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  27 in total

1.  Characterization of complexes of superhelical and relaxed closed circular DNA with H1 and phosphorylated H1 histones.

Authors:  D S Singer; M F Singer
Journal:  Biochemistry       Date:  1978-05-30       Impact factor: 3.162

2.  A rapid alkaline extraction procedure for screening recombinant plasmid DNA.

Authors:  H C Birnboim; J Doly
Journal:  Nucleic Acids Res       Date:  1979-11-24       Impact factor: 16.971

3.  Transcription of the constitutively expressed yeast enolase gene ENO1 is mediated by positive and negative cis-acting regulatory sequences.

Authors:  R Cohen; T Yokoi; J P Holland; A E Pepper; M J Holland
Journal:  Mol Cell Biol       Date:  1987-08       Impact factor: 4.272

4.  Identification of AAS genes and their regulatory role in general control of amino acid biosynthesis in yeast.

Authors:  M D Penn; B Galgoci; H Greer
Journal:  Proc Natl Acad Sci U S A       Date:  1983-05       Impact factor: 11.205

5.  Cloning of yeast glycolysis genes by complementation.

Authors:  G Kawasaki; D G Fraenkel
Journal:  Biochem Biophys Res Commun       Date:  1982-10-15       Impact factor: 3.575

6.  Regulation of genes controlling synthesis of the galactose pathway enzymes in yeast.

Authors:  H C Douglas; D C Hawthorne
Journal:  Genetics       Date:  1966-09       Impact factor: 4.562

7.  Targeted deletion of a yeast enolase structural gene. Identification and isolation of yeast enolase isozymes.

Authors:  L McAlister; M J Holland
Journal:  J Biol Chem       Date:  1982-06-25       Impact factor: 5.157

8.  DNA sequencing with chain-terminating inhibitors.

Authors:  F Sanger; S Nicklen; A R Coulson
Journal:  Proc Natl Acad Sci U S A       Date:  1977-12       Impact factor: 11.205

9.  Heme regulates transcription of the CYC1 gene of S. cerevisiae via an upstream activation site.

Authors:  L Guarente; T Mason
Journal:  Cell       Date:  1983-04       Impact factor: 41.582

10.  Repeated DNA sequences upstream from HIS1 also occur at several other co-regulated genes in Saccharomyces cerevisiae.

Authors:  A G Hinnebusch; G R Fink
Journal:  J Biol Chem       Date:  1983-04-25       Impact factor: 5.157

View more
  17 in total

1.  A REB1-binding site is required for GCN4-independent ILV1 basal level transcription and can be functionally replaced by an ABF1-binding site.

Authors:  J E Remacle; S Holmberg
Journal:  Mol Cell Biol       Date:  1992-12       Impact factor: 4.272

2.  Multiple factors bind the upstream activation sites of the yeast enolase genes ENO1 and ENO2: ABFI protein, like repressor activator protein RAP1, binds cis-acting sequences which modulate repression or activation of transcription.

Authors:  P K Brindle; J P Holland; C E Willett; M A Innis; M J Holland
Journal:  Mol Cell Biol       Date:  1990-09       Impact factor: 4.272

3.  Efficient transcription of the glycolytic gene ADH1 and three translational component genes requires the GCR1 product, which can act through TUF/GRF/RAP binding sites.

Authors:  G M Santangelo; J Tornow
Journal:  Mol Cell Biol       Date:  1990-02       Impact factor: 4.272

4.  Characterisation of the DNA binding domain of the yeast RAP1 protein.

Authors:  Y A Henry; A Chambers; J S Tsang; A J Kingsman; S M Kingsman
Journal:  Nucleic Acids Res       Date:  1990-05-11       Impact factor: 16.971

5.  The UAS of the yeast PGK gene is composed of multiple functional elements.

Authors:  A Chambers; C Stanway; A J Kingsman; S M Kingsman
Journal:  Nucleic Acids Res       Date:  1988-09-12       Impact factor: 16.971

6.  Mutational analysis of the upstream activation site of yeast ribosomal protein genes.

Authors:  R T Nieuwint; W H Mager; K C Maurer; R J Planta
Journal:  Curr Genet       Date:  1989-04       Impact factor: 3.886

7.  A regulatory element in the CHA1 promoter which confers inducibility by serine and threonine on Saccharomyces cerevisiae genes.

Authors:  C Bornaes; M W Ignjatovic; P Schjerling; M C Kielland-Brandt; S Holmberg
Journal:  Mol Cell Biol       Date:  1993-12       Impact factor: 4.272

8.  gcr2, a new mutation affecting glycolytic gene expression in Saccharomyces cerevisiae.

Authors:  H Uemura; D G Fraenkel
Journal:  Mol Cell Biol       Date:  1990-12       Impact factor: 4.272

9.  Elements involved in S-adenosylmethionine-mediated regulation of the Saccharomyces cerevisiae MET25 gene.

Authors:  D Thomas; H Cherest; Y Surdin-Kerjan
Journal:  Mol Cell Biol       Date:  1989-08       Impact factor: 4.272

10.  Mutations in GCR3, a gene involved in the expression of glycolytic genes in Saccharomyces cerevisiae, suppress the temperature-sensitive growth of hpr1 mutants.

Authors:  H Uemura; S Pandit; Y Jigami; R Sternglanz
Journal:  Genetics       Date:  1996-04       Impact factor: 4.562

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.