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J Biol Chem, Vol. 275, Issue 19, 14408-14414, May 12, 2000
From the Department of Microbiology and Immunology, University of
Tennessee, Memphis, Tennessee 38163
GATA family activators (Gln3p and Gat1p) and
repressors (Dal80p and Deh1p) regulate nitrogen catabolite repression
(NCR)-sensitive transcription in Saccharomyces cerevisiae
presumably via their competitive binding to the GATA sequences upstream
of NCR-sensitive genes. Ure2p, which is not a GATA family member,
inhibits Gln3p/Gat1p from functioning in the presence of good nitrogen
sources. We show that NCR-sensitive DAL80 transcription can
be influenced by the relative levels of GAT1 and
URE2 expression. NCR, normally observed with ammonia or
glutamine, is severely diminished when Gat1p is overproduced, and this
inhibition is overcome by simultaneously increasing URE2
expression. Further, overproduction of Ure2p nearly eliminates
NCR-sensitive transcription under derepressive growth conditions,
i.e. with proline as the sole nitrogen source. Enhanced green fluorescent protein-Gat1p is nuclear when
Gat1p-dependent transcription is high and cytoplasmic when
it is inhibited by overproduction of Ure2p.
Nitrogen Catabolite Repression of DAL80
Expression Depends on the Relative Levels of Gat1p and Ure2p
Production in Saccharomyces cerevisiae*
*
This work was supported by National Institutes of Health
Grant GM-35642.The costs of publication of this
article were defrayed in part by the
payment of page charges. The article
must therefore be hereby marked
"advertisement" in
accordance with 18 U.S.C. Section
1734 solely to indicate this fact.
To whom correspondence should be addressed. Tel.: 901-448-6175;
Fax: 901-448-8462; E-mail: tcooper@utmem.edu.
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