Abstract

We show by the following series of experiments that the yeast positive regulatory protein GAL4 binds to four sites in the upstream activating sequence UAS G to activate transcription of the adjacent GAL1 and GAL10 genes. GAL4 protein expressed in E. coli protected guanine residues in UAS G from methylation by dimethyl sulfate. The same set of protections was seen in vivo in yeast and depended on the GAL4 + allele. This protection pattern is consistent with the idea that GAL4 protein binds to four related 17 by sequences, each of which displays approximate 2-fold rotational symmetry. A single near-consensus synthetic 17 by oligonucleotide, installed in front of the yeast GAL1 or CYC1 transcription units, conferred a high level of galactose inducibility upon these genes. Further experiments suggest that one mechanism of glucose repression is inhibition of the binding of GALA protein to DNA.

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