Literature DB >> 8013904

Suppressors reveal two classes of glucose repression genes in the yeast Saccharomyces cerevisiae.

J R Erickson1, M Johnston.   

Abstract

We selected and analyzed extragenic suppressors of mutations in four genes--GRR1, REG1, GAL82 and GAL83-required for glucose repression of the GAL genes in the yeast Saccharomyces cerevisiae. The suppressors restore normal or nearly normal glucose repression of GAL1 expression in these glucose repression mutants. Tests of the ability of each suppressor to cross-suppress mutations in the other glucose repression genes revealed two groups of mutually cross-suppressed genes: (1) REG1, GAL82 and GAL83 and (2) GRR1. Mutations of a single gene, SRG1, were found as suppressors of reg1, GAL83-2000 and GAL82-1, suggesting that these three gene products act at a similar point in the glucose repression pathway. Mutations in SRG1 do not cross-suppress grr1 or hxk2 mutations. Conversely, suppressors of grr1 (rgt1) do not cross-suppress any other glucose repression mutation tested. These results, together with what was previously known about these genes, lead us to propose a model for glucose repression in which Grr1p acts early in the glucose repression pathway, perhaps affecting the generation of the signal for glucose repression. We suggest that Reg1p, Gal82p and Gal83p act after the step(s) executed by Grr1p, possibly transmitting the signal for repression to the Snf1p protein kinase.

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Year:  1994        PMID: 8013904      PMCID: PMC1205907     

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  25 in total

1.  Analysis of URSG-mediated glucose repression of the GAL1 promoter of Saccharomyces cerevisiae.

Authors:  J S Flick; M Johnston
Journal:  Genetics       Date:  1992-02       Impact factor: 4.562

Review 2.  Carbon catabolite repression in yeast.

Authors:  J M Gancedo
Journal:  Eur J Biochem       Date:  1992-06-01

3.  SRN1, a yeast gene involved in RNA processing, is identical to HEX2/REG1, a negative regulator in glucose repression.

Authors:  K S Tung; L L Norbeck; S L Nolan; N S Atkinson; A K Hopper
Journal:  Mol Cell Biol       Date:  1992-06       Impact factor: 4.272

4.  Genetic and molecular characterization of GAL83: its interaction and similarities with other genes involved in glucose repression in Saccharomyces cerevisiae.

Authors:  J R Erickson; M Johnston
Journal:  Genetics       Date:  1993-11       Impact factor: 4.562

5.  New SNF genes, GAL11 and GRR1 affect SUC2 expression in Saccharomyces cerevisiae.

Authors:  L G Vallier; M Carlson
Journal:  Genetics       Date:  1991-11       Impact factor: 4.562

6.  The COT2 gene is required for glucose-dependent divalent cation transport in Saccharomyces cerevisiae.

Authors:  D S Conklin; C Kung; M R Culbertson
Journal:  Mol Cell Biol       Date:  1993-04       Impact factor: 4.272

7.  Ssn6-Tup1 is a general repressor of transcription in yeast.

Authors:  C A Keleher; M J Redd; J Schultz; M Carlson; A D Johnson
Journal:  Cell       Date:  1992-02-21       Impact factor: 41.582

8.  Yeast SKO1 gene encodes a bZIP protein that binds to the CRE motif and acts as a repressor of transcription.

Authors:  J O Nehlin; M Carlberg; H Ronne
Journal:  Nucleic Acids Res       Date:  1992-10-25       Impact factor: 16.971

9.  Altered regulatory responses to glucose are associated with a glucose transport defect in grr1 mutants of Saccharomyces cerevisiae.

Authors:  L G Vallier; D Coons; L F Bisson; M Carlson
Journal:  Genetics       Date:  1994-04       Impact factor: 4.562

10.  Regulated expression of the GAL4 activator gene in yeast provides a sensitive genetic switch for glucose repression.

Authors:  D W Griggs; M Johnston
Journal:  Proc Natl Acad Sci U S A       Date:  1991-10-01       Impact factor: 11.205

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  21 in total

1.  Grr1 of Saccharomyces cerevisiae is connected to the ubiquitin proteolysis machinery through Skp1: coupling glucose sensing to gene expression and the cell cycle.

Authors:  F N Li; M Johnston
Journal:  EMBO J       Date:  1997-09-15       Impact factor: 11.598

2.  Genetic interactions between REG1/HEX2 and GLC7, the gene encoding the protein phosphatase type 1 catalytic subunit in Saccharomyces cerevisiae.

Authors:  D Huang; K T Chun; M G Goebl; P J Roach
Journal:  Genetics       Date:  1996-05       Impact factor: 4.562

3.  Glucose sensing and signaling by two glucose receptors in the yeast Saccharomyces cerevisiae.

Authors:  S Ozcan; J Dover; M Johnston
Journal:  EMBO J       Date:  1998-05-01       Impact factor: 11.598

4.  Multicopy FZF1 (SUL1) suppresses the sulfite sensitivity but not the glucose derepression or aberrant cell morphology of a grr1 mutant of Saccharomyces cerevisiae.

Authors:  D Avram; A T Bakalinsky
Journal:  Genetics       Date:  1996-10       Impact factor: 4.562

5.  Rgt1p of Saccharomyces cerevisiae, a key regulator of glucose-induced genes, is both an activator and a repressor of transcription.

Authors:  S Ozcan; T Leong; M Johnston
Journal:  Mol Cell Biol       Date:  1996-11       Impact factor: 4.272

6.  Regulation of nuclear genes encoding mitochondrial proteins in Saccharomyces cerevisiae.

Authors:  T A Brown; C Evangelista; B L Trumpower
Journal:  J Bacteriol       Date:  1995-12       Impact factor: 3.490

7.  The REG2 gene of Saccharomyces cerevisiae encodes a type 1 protein phosphatase-binding protein that functions with Reg1p and the Snf1 protein kinase to regulate growth.

Authors:  D L Frederick; K Tatchell
Journal:  Mol Cell Biol       Date:  1996-06       Impact factor: 4.272

Review 8.  Regulation of Cdc28 cyclin-dependent protein kinase activity during the cell cycle of the yeast Saccharomyces cerevisiae.

Authors:  M D Mendenhall; A E Hodge
Journal:  Microbiol Mol Biol Rev       Date:  1998-12       Impact factor: 11.056

Review 9.  Yeast carbon catabolite repression.

Authors:  J M Gancedo
Journal:  Microbiol Mol Biol Rev       Date:  1998-06       Impact factor: 11.056

10.  Regulatory network connecting two glucose signal transduction pathways in Saccharomyces cerevisiae.

Authors:  Aneta Kaniak; Zhixiong Xue; Daniel Macool; Jeong-Ho Kim; Mark Johnston
Journal:  Eukaryot Cell       Date:  2004-02
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