AbstractWe have identified in the promoter of the yeast FBP1 gene two sites able to bind nuclear proteins. These sites have a nucleotide sequence strongly similar to that of sites which bind the regulatory protein MIG1 in the promoters of GAL4 and SUC2. Deletions performed in the FBP1 promoter showed that one of the sites contributes to catabolite repression of this gene. In the same promoter, another region was identified with a strong effect on the catabolite repression of FBP1. In this region a sequence similar to the consensus for the binding site of the MIG1 protein was also present
All eukaryotic cells alter their transcriptional program in response to the sugar glucose. In Saccha...
The yeast Snflp kinase is required for normal expression of many genes involved in utilization of no...
Expression of the SUC2 gene in Saccharomyces cerevisiae, which encodes invertase, is repressed about...
We have identified in the promoter of the yeast FBP1 gene two sites able to bind nuclear proteins. T...
AbstractWe have identified in the promoter of the yeast FBP1 gene two sites able to bind nuclear pro...
AbstractBy deletion analysis of the fusion genes FBP1-lacZ and PCK1-lacZ we have identified a number...
By deletion analysis of the fusion genes FBP1-lacZ and PCK1-lacZ we have identified a number of stro...
In Saccharomyces cereisiae expression of the fructose-1,6-bisphosphatase-encoding gene, FBP1, is con...
The mechanism of catabolite repression in yeast is not well understood, although it has been establi...
We have investigated the effect of different carbon sources and of different mutations on the capaci...
Mig1p is a zinc finger protein required for repression of glucose-regulated genes in budding yeast. ...
AbstractTranscription of the vacuolar aminopeptidase yscI (APE1) gene in Saccharomyces cerevisiae ha...
All eukaryotic cells alter their transcriptional program in response to the sugar glucose. In Saccha...
AbstractE153 is a respiratory deficient mutant of Saccharomyces cerevisiae with a mutation in the ac...
AbstractMig1p is a zinc finger protein required for repression of glucose-regulated genes in budding...
All eukaryotic cells alter their transcriptional program in response to the sugar glucose. In Saccha...
The yeast Snflp kinase is required for normal expression of many genes involved in utilization of no...
Expression of the SUC2 gene in Saccharomyces cerevisiae, which encodes invertase, is repressed about...
We have identified in the promoter of the yeast FBP1 gene two sites able to bind nuclear proteins. T...
AbstractWe have identified in the promoter of the yeast FBP1 gene two sites able to bind nuclear pro...
AbstractBy deletion analysis of the fusion genes FBP1-lacZ and PCK1-lacZ we have identified a number...
By deletion analysis of the fusion genes FBP1-lacZ and PCK1-lacZ we have identified a number of stro...
In Saccharomyces cereisiae expression of the fructose-1,6-bisphosphatase-encoding gene, FBP1, is con...
The mechanism of catabolite repression in yeast is not well understood, although it has been establi...
We have investigated the effect of different carbon sources and of different mutations on the capaci...
Mig1p is a zinc finger protein required for repression of glucose-regulated genes in budding yeast. ...
AbstractTranscription of the vacuolar aminopeptidase yscI (APE1) gene in Saccharomyces cerevisiae ha...
All eukaryotic cells alter their transcriptional program in response to the sugar glucose. In Saccha...
AbstractE153 is a respiratory deficient mutant of Saccharomyces cerevisiae with a mutation in the ac...
AbstractMig1p is a zinc finger protein required for repression of glucose-regulated genes in budding...
All eukaryotic cells alter their transcriptional program in response to the sugar glucose. In Saccha...
The yeast Snflp kinase is required for normal expression of many genes involved in utilization of no...
Expression of the SUC2 gene in Saccharomyces cerevisiae, which encodes invertase, is repressed about...