This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Bysani, N
Right arrow Articles by Cooper, T G
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bysani, N
Right arrow Articles by Cooper, T G

 Previous Article  |  Next Article 

J Bacteriol. 1991 August; 173(16): 4977-4982

research-article

Saturation mutagenesis of the UASNTR (GATAA) responsible for nitrogen catabolite repression-sensitive transcriptional activation of the allantoin pathway genes in Saccharomyces cerevisiae.

N Bysani, J R Daugherty and T G Cooper

Department of Microbiology and Immunology, University of Tennessee, Memphis 38163.

ABSTRACT

Saturation mutagenesis of the UASNTR element responsible for GLN3-dependent, nitrogen catabolite repression-sensitive transcriptional activation of allantoin pathway genes in yeast cells identified the dodecanucleotide sequence 5'-TTNCTGATAAGG-3' as the minimum required for UAS activity. There was significant flexibility in mutant sequences capable of supporting UAS activity, which correlates well with the high variation in UASNTR homologous sequences reported to be upstream of the DAL and DUR genes. Three of nine UASNTR-like sequences 5' of the DAL5 gene supported high-level transcriptional activation. The others, which contained nonpermissive substitutions, were not active.


J Bacteriol. 1991 August; 173(16): 4977-4982




This article has been cited by other articles:

  • Chen, G., Hata, N., Zhang, M. Q. (2004). Transcription factor binding element detection using functional clustering of mutant expression data. Nucleic Acids Res 32: 2362-2371 [Abstract] [Full Text]  
  • Vuralhan, Z., Morais, M. A., Tai, S.-L., Piper, M. D. W., Pronk, J. T. (2003). Identification and Characterization of Phenylpyruvate Decarboxylase Genes in Saccharomyces cerevisiae. Appl. Environ. Microbiol. 69: 4534-4541 [Abstract] [Full Text]  
  • Boer, V. M., de Winde, J. H., Pronk, J. T., Piper, M. D. W. (2003). The Genome-wide Transcriptional Responses of Saccharomyces cerevisiae Grown on Glucose in Aerobic Chemostat Cultures Limited for Carbon, Nitrogen, Phosphorus, or Sulfur. J. Biol. Chem. 278: 3265-3274 [Abstract] [Full Text]  
  • Gojkovic, Z., Sandrini, M. P. B., Piskur, J. (2001). Eukaryotic {beta}-Alanine Synthases Are Functionally Related but Have a High Degree of Structural Diversity. Genetics 158: 999-1011 [Abstract] [Full Text]  
  • Beeser, A. E., Cooper, T. G. (2000). The Dual-Specificity Protein Phosphatase Yvh1p Regulates Sporulation, Growth, and Glycogen Accumulation Independently of Catalytic Activity in Saccharomyces cerevisiae via the Cyclic AMP-Dependent Protein Kinase Cascade. J. Bacteriol. 182: 3517-3528 [Abstract] [Full Text]  
  • Cunningham, T. S., Andhare, R., Cooper, T. G. (2000). Nitrogen Catabolite Repression of DAL80 Expression Depends on the Relative Levels of Gat1p and Ure2p Production in Saccharomyces cerevisiae. J. Biol. Chem. 275: 14408-14414 [Abstract] [Full Text]  
  • Scott, S., Dorrington, R., Svetlov, V., Beeser, A. E., Distler, M., Cooper, T. G. (2000). Functional Domain Mapping and Subcellular Distribution of Dal82p in Saccharomyces cerevisiae. J. Biol. Chem. 275: 7198-7204 [Abstract] [Full Text]  
  • Rai, R., Daugherty, J. R., Cunningham, T. S., Cooper, T. G. (1999). Overlapping Positive and Negative GATA Factor Binding Sites Mediate Inducible DAL7 Gene Expression in Saccharomyces cerevisiae. J. Biol. Chem. 274: 28026-28034 [Abstract] [Full Text]  
  • Svetlov, V. V., Cooper, T. G. (1998). The Saccharomyces cerevisiae GATA Factors Dal80p and Deh1p Can Form Homo- and Heterodimeric Complexes. J. Bacteriol. 180: 5682-5688 [Abstract] [Full Text]  
  • Cox, K. H., Rai, R., Distler, M., Daugherty, J. R., Coffman, J. A., Cooper, T. G. (2000). Saccharomyces cerevisiae GATA Sequences Function as TATA Elements during Nitrogen Catabolite Repression and When Gln3p Is Excluded from the Nucleus by Overproduction of Ure2p. J. Biol. Chem. 275: 17611-17618 [Abstract] [Full Text]