Affiliation:
1. Department of Microbiology and Immunology, University of Tennessee, Memphis, Tennessee 38163
Abstract
ABSTRACT
Nitrogen-catabolic gene expression in
Saccharomyces cerevisiae
is regulated by the action of four GATA family transcription factors: Gln3p and Gat1p/Nil1p are transcriptional activators, and Dal80 and Deh1p/Gzf3p are repressors. In addition to the GATA sequences situated upstream of all nitrogen catabolite repression-sensitive genes that encode enzyme and transport proteins, the promoters of the
GAT1
,
DAL80
, and
DEH1
genes all contain multiple GATA sequences as well. These GATA sequences are the binding sites of the GATA family transcription factors and are hypothesized to mediate their autogenous and cross regulation. Here we show, using
DAL80
fused to the carbon-regulated
GAL1
,
10
or copper-regulated
CUP1
promoter, that
GAT1
expression is inversely regulated by the level of
DAL80
expression, i.e., as
DAL80
expression increases,
GAT1
expression decreases. The amount of
DAL80
expression also dictates the level at which
DAL3
, a gene activated almost exclusively by Gln3p, is transcribed. Gat1p was found to partially substitute for Gln3p in transcription. These data support the contention that regulation of GATA-factor gene expression is tightly and dynamically coupled. Finally, we suggest that the complicated regulatory circuit in which the GATA family transcription factors participate is probably most beneficial as cells make the transition from excess to limited nitrogen availability.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology