Saccharomyces cerevisiae GATA Sequences Function as TATA Elements during Nitrogen Catabolite Repression and When Gln3p Is Excluded from the Nucleus by Overproduction of Ure2p
Open Access
- 1 June 2000
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 275 (23) , 17611-17618
- https://doi.org/10.1074/jbc.m001648200
Abstract
No abstract availableKeywords
This publication has 43 references indexed in Scilit:
- The transcriptional profile of Saccharomyces cerevisiae exposed to rapamycin mimics the profile induced by amino acid starvationNature Genetics, 1999
- Kinase Activity-dependent Nuclear Export Opposes Stress-induced Nuclear Accumulation and Retention of Hog1 Mitogen-activated Protein Kinase in the Budding YeastSaccharomyces cerevisiaeMolecular Biology of the Cell, 1999
- The phosphatase system in Saccharomyces cerevisiae.Genes & Genetic Systems, 1997
- [URE3] as an Altered URE2 Protein: Evidence for a Prion Analog in Saccharomyces cerevisiaeScience, 1994
- The erythroid-specific protein cGATA-1 mediates distal enhancer activity through a specialized beta-globin TATA box.Genes & Development, 1992
- A wide variety of DNA sequences can functionally replace a yeast TATA element for transcriptional activation.Genes & Development, 1990
- Saturation mutagenesis of a yeast his3 "TATA element": genetic evidence for a specific TATA-binding protein.Proceedings of the National Academy of Sciences, 1988
- The complete coding sequence of the human raf oncogene and the corresponding structure of the c-raf-1 geneNucleic Acids Research, 1986
- Yeast mutants pleiotropically impaired in the regulation of the two glutamate dehydrogenasesBiochemical and Biophysical Research Communications, 1973
- Multiplicity of the amino acid permeases in Saccharomyces cerevisiaeBiochimica et Biophysica Acta (BBA) - General Subjects, 1966