Search results for "Enzyme Repression"

showing 4 items of 4 documents

Multiple copies of SUC4 regulatory regions may cause partial de-repression of invertase synthesis in Saccharomyces cerevisiae.

1992

Transformation to generate multiple copies of regulatory DNA sequences has been used to study the interactions between regulatory proteins and their target sequences, since a high copy number of these sequences may titrate trans-acting regulatory proteins. We have analyzed the synthesis of invertase in yeast strains carrying different SUC genes transformed with the multiple-copy plasmid pSH143, a derivative of pJDB207 containing the promoter and upstream regulatory sequences of SUC4. The results obtained seem to be strain dependent. Under repressing conditions a high copy number of SUC4 promoter regions may cause increased expression of the invertase genes resulting in the synthesis of exte…

ElectrophoresisGlycoside HydrolasesSaccharomyces cerevisiaeGenes FungalMolecular Sequence DataSaccharomyces cerevisiaePlasmidGene Expression Regulation FungalGeneticsPromoter Regions GeneticGeneRepetitive Sequences Nucleic AcidRegulation of gene expressionGeneticsBinding SitesbiologyBase Sequencebeta-FructofuranosidaseFungal geneticsPromoterGeneral Medicinebiology.organism_classificationInvertaseGlucoseRegulatory sequenceEnzyme RepressionPlasmidsCurrent genetics
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Molecular events associated with glucose repression of invertase in Saccharomyces cerevisiae.

1986

When S. cerevisiae growing in the presence of glucose (repressive condition) was shifted to higher temperatures, invertase was secreted. This secretion required protein synthesis, but was independent of RNA formation (Mormeneo & Sentandreu 1982). In addition accumulation of invertasespecific messenger RNA occurred in the absence of protein synthesis but was expressed only after synthesis of protein. Invertase mRNA was continuously synthesized under repressive conditions and the levels of this mRNA were regulated by the presence of glucose. The hexose regulated the concentration of this mRNA at the level of transcription and/or by sensitization of this messenger RNA. The expression of the in…

Glycoside HydrolasesTranscription GeneticSaccharomyces cerevisiaeSaccharomyces cerevisiaeCycloheximideBiologyMicrobiologyEnzyme Repressionchemistry.chemical_compoundTranscription (biology)Protein biosynthesisRNA MessengerCycloheximideMaltoseMolecular BiologyMessenger RNAbeta-FructofuranosidaseTemperatureRNA FungalGeneral MedicineMaltosebiology.organism_classificationCulture MediaInvertaseGlucoseBiochemistrychemistryEnzyme RepressionAntonie van Leeuwenhoek
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Fine analysis of the chromatin structure of the yeast SUC2 gene and of its changes upon derepression. Comparison between the chromosomal and plasmid-…

1987

Micrococcal nuclease digestion has been used to investigate some fine details of the chromatin structure of the yeast SUC2 gene for invertase. Precisely positioned nucleosomes have been found on a 2 kb sequence from the 3' non-coding region, and four nucleosomes also seem to occupy fixed positions on the 5' flank. Eleven nucleosomes lie on the coding region, although their positioning is not as precise as in the flanks. When the gene is derepressed, these latter nucleosomes adopt a more open conformation and so do two of the nucleosomes positioned on the 5' flank. A dramatic change occurs in the 3' flank, whose involvement in the structural transitions of chromatin upon gene activation is p…

Regulation of gene expressionGeneticsbiologyGlycoside Hydrolasesbeta-FructofuranosidaseGenes FungalChromosomeDNA Restriction EnzymesSaccharomyces cerevisiaeChromatinChromatinNucleosomesPlasmidGenesGeneticsbiology.proteinNucleosomeCoding regionMicrococcal NucleaseEnzyme RepressionDerepressionMicrococcal nuclease
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Differential Translational Efficiency of the mRNAs Isolated from Derepressed and Glucose Repressed Saccharomyces cerevisiae

1987

Summary: Carbon catabolite derepression induced changes in the pool of yeast mRNAs translatable in a protein-synthesizing reticulocyte system. Competition experiments with globin mRNA showed that the mRNA population obtained from derepressed cells possessed a higher translational efficiency than mRNA from repressed cells. The mRNAs that could account for the high translational efficiency of the derepressed mRNA were not detected in cells growing in glucose-rich medium. Analysis of protein synthesis in the presence of 7-methylguanosine 5′-phosphate indicated that the initiation factors recognizing the 5′-terminal structure of capped messengers interacted with lower affinity with the represse…

education.field_of_studyTranslational efficiencyfungiPopulationSaccharomyces cerevisiaeCatabolite repressionRNA FungalSaccharomyces cerevisiaeBiologybiology.organism_classificationMicrobiologyFungal ProteinsKineticsGlucosemedicine.anatomical_structureReticulocyteBiochemistryProtein BiosynthesismedicineProtein biosynthesisInitiation factorRNA MessengerEnzyme RepressioneducationDerepressionMicrobiology
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