The GLN3 gene product is required for transcriptional activation of allantoin system gene expression in Saccharomyces cerevisiae

Author:

Cooper T G1,Ferguson D1,Rai R1,Bysani N1

Affiliation:

1. Department of Microbiology and Immunology, University of Tennessee, Memphis 38163.

Abstract

We show that mutation at the GLN3 locus results in decreased steady-state levels of DAL7, DUR1,2, CAR1, and URA3 mRNAs derived from cultures grown in the presence of inducer. Basal levels of these RNA species, however, were not significantly affected by a gln3 mutation. The GLN3 product appears to affect gene expression in two ways. The pleiotropic requirement of GLN3 for induced gene expression probably derives from the need of the GLN3 product for inducer uptake into the cell and its loss in gln3 mutants. We also demonstrate that transcriptional activation, mediated by the DAL5 and DAL7 upstream activation sequences, requires a functional GLN3 gene product. This observation identified transcriptional activation as the most likely point of GLN3 participation in the expression of allantoin system genes.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

Reference21 articles.

1. Three regulatory systems control expression of glutamine synthetase in Saccharomyces cerevisiae at the level of transcription;Benjamin P. J.;Mol. Gen. Genet.,1989

2. Oxalurate induction of multiple URAJ transcripts in Saccharonyces cerevisiae;Buckholz R.;Mol. Cell. Biol.,1983

3. Cooper T. G. 1982. Nitrogen metabolism in Saccharomyces cerevisiae p. 39-99. In J. Strathern E. Jones and J. R. Broach (ed.) Molecular biology of the yeast Saccharomyces: metabolism and gene expression. Cold Spring Harbor Laboratory Cold Spring Harbor N.Y.

4. Requirement of upstream activation sequences for nitrogen catabolite repression of the allantoin system genes in Saccharomyces cerevisiae;Cooper T. G.;Mol. Cell. Biol.,1989

5. Regulation of nitrogen assimilation in Saccharomyces cerevisiae: roles of the URE2 and GLN3 genes;Courchesne W. E.;J. Bacteriol.,1988

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