Literature DB >> 1682801

Role of the complex upstream region of the GDH2 gene in nitrogen regulation of the NAD-linked glutamate dehydrogenase in Saccharomyces cerevisiae.

S M Miller1, B Magasanik.   

Abstract

We analyzed the upstream region of the GDH2 gene, which encodes the NAD-linked glutamate dehydrogenase in Saccharomyces cerevisiae, for elements important for the regulation of the gene by the nitrogen source. The levels of this enzyme are high in cells grown with glutamate as the sole source of nitrogen and low in cells grown with glutamine or ammonium. We found that this regulation occurs at the level of transcription and that a total of six sites are required to cause a CYC1-lacZ fusion to the GDH2 gene to be regulated in the same manner as the NAD-linked glutamate dehydrogenase. Two sites behaved as upstream activation sites (UASs). The remaining four sites were found to block the effects of the two UASs in such a way that the GDH2-CYC1-lacZ fusion was not expressed unless the cells containing it were grown under conditions favorable for the activity of both UASs. This complex regulatory system appears to account for the fact that GDH2 expression is exquisitely sensitive to glutamine, whereas the expression of GLN1, coding for glutamine synthetase, is not nearly as sensitive.

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Year:  1991        PMID: 1682801      PMCID: PMC361811          DOI: 10.1128/mcb.11.12.6229-6247.1991

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  58 in total

1.  THE PATHWAY OF ARGININE BREAKDOWN IN SACCHAROMYCES CEREVISIAE.

Authors:  W J MIDDELHOVEN
Journal:  Biochim Biophys Acta       Date:  1964-12-09

2.  Identification of sequences responsible for transcriptional activation of the allantoate permease gene in Saccharomyces cerevisiae.

Authors:  R Rai; F S Genbauffe; R A Sumrada; T G Cooper
Journal:  Mol Cell Biol       Date:  1989-02       Impact factor: 4.272

3.  Sequence and expression of GLN3, a positive nitrogen regulatory gene of Saccharomyces cerevisiae encoding a protein with a putative zinc finger DNA-binding domain.

Authors:  P L Minehart; B Magasanik
Journal:  Mol Cell Biol       Date:  1991-12       Impact factor: 4.272

4.  The URE2 gene product of Saccharomyces cerevisiae plays an important role in the cellular response to the nitrogen source and has homology to glutathione s-transferases.

Authors:  P W Coschigano; B Magasanik
Journal:  Mol Cell Biol       Date:  1991-02       Impact factor: 4.272

5.  Possible failure of NADP-glutamate dehydrogenase to participate directly in nitrogen repression of the allantoin degradative enzymes in Saccharomyces cerevisiae.

Authors:  J Bossinger; T Cooper
Journal:  Biochem Biophys Res Commun       Date:  1975-10-06       Impact factor: 3.575

6.  Requirement of upstream activation sequences for nitrogen catabolite repression of the allantoin system genes in Saccharomyces cerevisiae.

Authors:  T G Cooper; R Rai; H S Yoo
Journal:  Mol Cell Biol       Date:  1989-12       Impact factor: 4.272

7.  Role of integration host factor in the regulation of the glnHp2 promoter of Escherichia coli.

Authors:  F Claverie-Martin; B Magasanik
Journal:  Proc Natl Acad Sci U S A       Date:  1991-03-01       Impact factor: 11.205

8.  Site-directed mutagenesis of the 'zinc finger' DNA-binding domain of the nitrogen-regulatory protein NIT2 of Neurospora.

Authors:  Y H Fu; G A Marzluf
Journal:  Mol Microbiol       Date:  1990-11       Impact factor: 3.501

9.  Activation of yeast polymerase II transcription by herpesvirus VP16 and GAL4 derivatives in vitro.

Authors:  D I Chasman; J Leatherwood; M Carey; M Ptashne; R D Kornberg
Journal:  Mol Cell Biol       Date:  1989-11       Impact factor: 4.272

10.  Physiological and genetic analysis of the carbon regulation of the NAD-dependent glutamate dehydrogenase of Saccharomyces cerevisiae.

Authors:  P W Coschigano; S M Miller; B Magasanik
Journal:  Mol Cell Biol       Date:  1991-09       Impact factor: 4.272

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  30 in total

1.  Tor1/2 regulation of retrograde gene expression in Saccharomyces cerevisiae derives indirectly as a consequence of alterations in ammonia metabolism.

Authors:  Jennifer J Tate; Terrance G Cooper
Journal:  J Biol Chem       Date:  2003-07-07       Impact factor: 5.157

2.  Sequence of the GLN1 gene of Saccharomyces cerevisiae: role of the upstream region in regulation of glutamine synthetase expression.

Authors:  P L Minehart; B Magasanik
Journal:  J Bacteriol       Date:  1992-03       Impact factor: 3.490

3.  Purification of the heteromeric protein binding to the URS1 transcriptional repression site in Saccharomyces cerevisiae.

Authors:  R M Luche; W C Smart; T G Cooper
Journal:  Proc Natl Acad Sci U S A       Date:  1992-08-15       Impact factor: 11.205

4.  Constitutive turnover of histone H2A.Z at yeast promoters requires the preinitiation complex.

Authors:  Michael Tramantano; Lu Sun; Christy Au; Daniel Labuz; Zhimin Liu; Mindy Chou; Chen Shen; Ed Luk
Journal:  Elife       Date:  2016-07-20       Impact factor: 8.140

5.  Sequence and expression of GLN3, a positive nitrogen regulatory gene of Saccharomyces cerevisiae encoding a protein with a putative zinc finger DNA-binding domain.

Authors:  P L Minehart; B Magasanik
Journal:  Mol Cell Biol       Date:  1991-12       Impact factor: 4.272

6.  G1n3p is capable of binding to UAS(NTR) elements and activating transcription in Saccharomyces cerevisiae.

Authors:  T S Cunningham; V V Svetlov; R Rai; W Smart; T G Cooper
Journal:  J Bacteriol       Date:  1996-06       Impact factor: 3.490

7.  The yeast UME6 gene product is required for transcriptional repression mediated by the CAR1 URS1 repressor binding site.

Authors:  H D Park; R M Luche; T G Cooper
Journal:  Nucleic Acids Res       Date:  1992-04-25       Impact factor: 16.971

8.  The concentration of ammonia regulates nitrogen metabolism in Saccharomyces cerevisiae.

Authors:  E G ter Schure; H H Silljé; A J Verkleij; J Boonstra; C T Verrips
Journal:  J Bacteriol       Date:  1995-11       Impact factor: 3.490

9.  Two transcription factors, Gln3p and Nil1p, use the same GATAAG sites to activate the expression of GAP1 of Saccharomyces cerevisiae.

Authors:  M Stanbrough; B Magasanik
Journal:  J Bacteriol       Date:  1996-04       Impact factor: 3.490

10.  Genetic evidence for Gln3p-independent, nitrogen catabolite repression-sensitive gene expression in Saccharomyces cerevisiae.

Authors:  J A Coffman; R Rai; T G Cooper
Journal:  J Bacteriol       Date:  1995-12       Impact factor: 3.490

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