Literature DB >> 7031056

The gcr (glycolysis regulation) mutation of Saccharomyces cerevisiae.

D Clifton, D G Fraenkel.   

Abstract

gcr is a mutation considerably decreasing the assayed amounts of most glycolysis enzymes in Saccharomyces cerevisiae (Clifton, D., Weinstock, S. B., and Fraenkel, D. G. (1978) Genetics 88, 1-11). We show here that although in the wild type strain the amounts of these enzymes do not greatly differ between cells from different media, in the gcr mutant strain most of the enzyme amounts are 5% or less, relative to wild type, from cells grown without sugars, but 20-50% from cells grown with sugars. Lower relative values were found for phosphoglycerate mutase and enolase. A corresponding alteration in the mutant in the intensities of several major protein bands could even be seen in stained gels after electrophoresis of crude extracts: the profiles were otherwise normal. Results of titration of phosphoglycerate kinase with antibody accorded with activity. Transfer of cells between the two types of media did not lead to a more rapid adjustment of enzyme amounts than expected from the steady state levels. gcr is not allelic to GPM (the gene for phosphoglycerate mutase) or to RNA1 (which affects transport of RNA from the nucleus). Translation of total RNA in a rabbit reticulocyte lysate gave a pattern of polypeptides similar to the in vivo one. Thus, gcr is likely to affect somehow mRNA synthesis or lifetime for a discrete number of proteins.

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Year:  1981        PMID: 7031056

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  58 in total

1.  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

2.  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

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.  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

5.  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

6.  The glucose-dependent transactivation activity of ABF1 on the expression of the TDH3 gene in yeast.

Authors:  S Y Jung; H Y Yoo; Y H Kim; J Kim; H M Rho
Journal:  Curr Genet       Date:  1995-03       Impact factor: 3.886

7.  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

8.  Identification of a regulatory region that mediates glucose-dependent induction of the Saccharomyces cerevisiae enolase gene ENO2.

Authors:  R Cohen; J P Holland; T Yokoi; M J Holland
Journal:  Mol Cell Biol       Date:  1986-07       Impact factor: 4.272

9.  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

10.  Coordinated regulation and inositol-mediated and fatty acid-mediated repression of fatty acid synthase genes in Saccharomyces cerevisiae.

Authors:  S S Chirala
Journal:  Proc Natl Acad Sci U S A       Date:  1992-11-01       Impact factor: 11.205

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