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Mol. Cell. Biol., 03 1996, 847-858, Vol 16, No. 3
JA Coffman, R Rai, T Cunningham, V Svetlov and TG Cooper
Saccharomyces cerevisiae cells selectively use nitrogen sources in their
environment. Nitrogen catabolite repression (NCR) is the basis of this
selectivity. Until recently NCR was thought to be accomplished exclusively
through the negative regulation of Gln3p function by Ure2p. The
demonstration that NCR-sensitive expression of multiple nitrogen- catabolic
genes occurs in a gln3 delta ure2 delta dal80::hisG triple mutant indicated
that the prevailing view of the nitrogen regulatory circuit was in need of
revision; additional components clearly existed. Here we demonstrate that
another positive regulator, designated Gat1p, participates in the
transcription of NCR-sensitive genes and is able to weakly activate
transcription when tethered upstream of a reporter gene devoid of upstream
activation sequence elements. Expression of GAT1 is shown to be NCR
sensitive, partially Gln3p dependent, and Dal80p regulated. In agreement
with this pattern of regulation, we also demonstrate the existence of Gln3p
and Dal80p binding sites upstream of GAT1.
Copyright © 1996, American Society for Microbiology
Gat1p, a GATA family protein whose production is sensitive to nitrogen catabolite repression, participates in transcriptional activation of nitrogen-catabolic genes in Saccharomyces cerevisiae
Department of Microbiology and Immunology, University of Tennessee, Memphis 38163, USA.
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