Opposing regulatory functions of positive and negative elements in UASG control transcription of the yeast GAL genes.
Open Access
- 31 October 1990
- journal article
- research article
- Published by Taylor & Francis in Molecular and Cellular Biology
- Vol. 10 (11) , 5663-5670
- https://doi.org/10.1128/mcb.10.11.5663
Abstract
The yeast GAL1 and GAL10 genes are transcribed at a remarkably low basal level when galactose is unavailable and are induced by over 4 orders of magnitude when it becomes available. Approximately six negative control elements (designated GAL operators GALO1 to GALO6) are located adjacent to or overlapping four binding sites for the transcription activator GAL4 in the GAL upstream activating sequence UASG. The negative control elements contribute to the broad range of inducibility of GAL1 and GAL10 by inhibiting two GAL4/galactose-independent activating elements (GAE1 and GAE2) in UASG. In turn, multiple GAL4-binding sites in UASG are necessary for GAL4 to overcome repression by the negative control elements under fully inducing conditions. When glucose in addition to galactose is available (repressing conditions), the ability of GAL4 to activate transcription is diminished as a result of its reduced affinity for DNA and the reduced availability of inducer. Under these conditions, the negative control elements inhibit transcriptional activation from the glucose-attenuated GAL4 sites, thus accounting at least in part for glucose repression acting in cis. A normal part of transcriptional regulation of the GAL1 and GAL10 genes, therefore, appears to involve a balance between the opposing functions of positive and negative control elements.This publication has 40 references indexed in Scilit:
- A yeast protein that influences the chromatin structure of UASG and functions as a powerful auxiliary gene activator.Genes & Development, 1990
- Specific protein binding to far upstream activating sequences in polymerase II promoters.Proceedings of the National Academy of Sciences, 1985
- Upstream activation sites of the CYC1 gene of Saccharomyces cerevisiae are active when inverted but not when placed downstream of the "TATA box".Proceedings of the National Academy of Sciences, 1984
- A bacterial repressor protein or a yeast transcriptional terminator can block upstream activation of a yeast geneNature, 1984
- Saccharomyces cerevisiae GAL1-GAL10 divergent promoter region: location and function of the upstream activating sequence UASG.Molecular and Cellular Biology, 1984
- Use of lacZ fusions to delimit regulatory elements of the inducible divergent GAL1-GAL10 promoter in Saccharomyces cerevisiae.Molecular and Cellular Biology, 1984
- Sequences that regulate the divergent GAL1-GAL10 promoter in Saccharomyces cerevisiae.Molecular and Cellular Biology, 1984
- Heme regulates transcription of the CYC1 gene of S. cerevisiae via an upstream activation siteCell, 1983
- A GAL10-CYC1 hybrid yeast promoter identifies the GAL4 regulatory region as an upstream site.Proceedings of the National Academy of Sciences, 1982
- Fusion of Escherichia coli lacZ to the cytochrome c gene of Saccharomyces cerevisiae.Proceedings of the National Academy of Sciences, 1981