Literature DB >> 1946357

GCR1 of Saccharomyces cerevisiae encodes a DNA binding protein whose binding is abolished by mutations in the CTTCC sequence motif.

H V Baker1.   

Abstract

In Saccharomyces cerevisiae, glycolysis enzymes constitute 30-60% of the soluble protein. GCR1 gene function is required for high-level glycolytic gene expression. In gcr1 mutant strains the levels of most glycolytic enzymes are between 2% and 10% of wild type. Binding sites for the global regulatory protein known as repressor activator protein 1 (RAP1)/general regulatory factor 1 (GRF1)/translation upstream factor (TUF) are found in close proximity to one or more CTTCC sequence motifs in the controlling region of GCR1-dependent genes. RAP1/GRF1/TUF-binding sites are known to be essential elements of upstream activating sequences that control expression of many glycolytic genes. In this report, I demonstrate that GCR1 encodes a DNA binding protein whose ability to bind DNA is dependent on the CTTCC sequence motif. This finding, in addition to the work of others, suggests that the GCR1 gene product and the RAP1/GRF1/TUF gene product act in concert to mediate high-level glycolytic gene expression.

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Year:  1991        PMID: 1946357      PMCID: PMC52734          DOI: 10.1073/pnas.88.21.9443

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  28 in total

1.  Characterization of TPI gene expression in isogeneic wild-type and gcr1-deletion mutant strains of Saccharomyces cerevisiae.

Authors:  E W Scott; H E Allison; H V Baker
Journal:  Nucleic Acids Res       Date:  1990-12-11       Impact factor: 16.971

2.  Cooperation of glycolytic enzymes.

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Journal:  Adv Enzyme Regul       Date:  1969

3.  Equilibria and kinetics of lac repressor-operator interactions by polyacrylamide gel electrophoresis.

Authors:  M Fried; D M Crothers
Journal:  Nucleic Acids Res       Date:  1981-12-11       Impact factor: 16.971

4.  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

5.  One-step purification of hybrid proteins which have beta-galactosidase activity.

Authors:  A Ullmann
Journal:  Gene       Date:  1984 Jul-Aug       Impact factor: 3.688

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Authors:  D Clifton; D G Fraenkel
Journal:  J Biol Chem       Date:  1981-12-25       Impact factor: 5.157

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Authors:  D Clifton; S B Weinstock; D G Fraenkel
Journal:  Genetics       Date:  1978-01       Impact factor: 4.562

8.  Nucleotide sequence of the triose phosphate isomerase gene of Saccharomyces cerevisiae.

Authors:  T Alber; G Kawasaki
Journal:  J Mol Appl Genet       Date:  1982

9.  A gel electrophoresis method for quantifying the binding of proteins to specific DNA regions: application to components of the Escherichia coli lactose operon regulatory system.

Authors:  M M Garner; A Revzin
Journal:  Nucleic Acids Res       Date:  1981-07-10       Impact factor: 16.971

10.  A general upstream binding factor for genes of the yeast translational apparatus.

Authors:  J Huet; P Cottrelle; M Cool; M L Vignais; D Thiele; C Marck; J M Buhler; A Sentenac; P Fromageot
Journal:  EMBO J       Date:  1985-12-16       Impact factor: 11.598

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  46 in total

1.  Transcript quantitation in total yeast cellular RNA using kinetic PCR.

Authors:  J J Kang; R M Watson; M E Fisher; R Higuchi; D H Gelfand; M J Holland
Journal:  Nucleic Acids Res       Date:  2000-01-15       Impact factor: 16.971

2.  Rap1p requires Gcr1p and Gcr2p homodimers to activate ribosomal protein and glycolytic genes, respectively.

Authors:  S J Deminoff; G M Santangelo
Journal:  Genetics       Date:  2001-05       Impact factor: 4.562

Review 3.  The unique features of glycolytic pathways in Archaea.

Authors:  Corné H Verhees; Servé W M Kengen; Judith E Tuininga; Gerrit J Schut; Michael W W Adams; Willem M De Vos; John Van Der Oost
Journal:  Biochem J       Date:  2003-10-15       Impact factor: 3.857

Review 4.  Multifunctional DNA-binding proteins in yeast.

Authors:  T Doorenbosch; W H Mager; R J Planta
Journal:  Gene Expr       Date:  1992

5.  Regulation of the hypoxic response in Candida albicans.

Authors:  John M Synnott; Alessandro Guida; Siobhan Mulhern-Haughey; Desmond G Higgins; Geraldine Butler
Journal:  Eukaryot Cell       Date:  2010-09-24

6.  The expression of PHO92 is regulated by Gcr1, and Pho92 is involved in glucose metabolism in Saccharomyces cerevisiae.

Authors:  Hyun-Jun Kang; Miwha Chang; Chang-Min Kang; Yong-Sung Park; Bong-June Yoon; Tae-Hyoung Kim; Cheol-Won Yun
Journal:  Curr Genet       Date:  2014-05-22       Impact factor: 3.886

7.  Regulation of glycolysis in Kluyveromyces lactis: role of KlGCR1 and KlGCR2 in glucose uptake and catabolism.

Authors:  H Neil; M Lemaire; M Wésolowski-Louvel
Journal:  Curr Genet       Date:  2003-12-19       Impact factor: 3.886

8.  The yeast protein Gcr1p binds to the PGK UAS and contributes to the activation of transcription of the PGK gene.

Authors:  Y A Henry; M C López; J M Gibbs; A Chambers; S M Kingsman; H V Baker; C A Stanway
Journal:  Mol Gen Genet       Date:  1994-11-15

9.  Activation mechanism of the multifunctional transcription factor repressor-activator protein 1 (Rap1p).

Authors:  C M Drazinic; J B Smerage; M C López; H V Baker
Journal:  Mol Cell Biol       Date:  1996-06       Impact factor: 4.272

10.  A simple in vivo footprinting method to examine DNA-protein interactions over the yeast PYK UAS element.

Authors:  I Dumitru; J B McNeil
Journal:  Nucleic Acids Res       Date:  1994-04-25       Impact factor: 16.971

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