Expression of GUT1, which encodes glycerol kinase in Saccharomyces cerevisiae, is controlled by the positive regulators Adr1p, Ino2p and Ino4p and the negative regulator Opi1p in a carbon source-dependent fashion

In Saccharomyces cerevisiae glycerol utilization is mediated by two enzymes , glycerol kinase (Gut1p) and mitochondrial glycerol-3-phosphate dehydrogen ase (Gut2p), The carbon source regulation of GUT1 was studied using promote r-reporter gene fusions, The promoter activity was lowest during growth on glucose and highest on the non-fermentable carbon sources, glycerol, ethano l, lactate, acetate and oleic acid. Mutational analysis of the GUT1 promote r region showed that two upstream activation sequences, UAS(INO) and UAS(AD R1), are responsible for similar to 90% of the expression during growth on glycerol, UAS(ADR1) is a presumed binding site for the zinc finger transcri ption factor Adr1p and UAS(INO) is a presumed binding site for the basic he lix-loop-helix transcription factors lno2p and lno4p. In vitro experiments showed Adr1 and lno2/lno4 protein-dependent binding to UAS(ADR1) and UAS(IN O). The negative regulator Opi1p mediates repression of the GUTI promoter, whereas the effects of the glucose repressors Mig1p and Mig2p are minor. To gether, the experiments show that GUTI is carbon source regulated by differ ent activation and repression systems.