Search results for "Saccharomyces cerevisiae"

showing 10 items of 738 documents

Differential expression of SUC genes: A question of bases

1994

Non-coding nucleotide sequences located 5' upstream of the transcriptional start site play an essential role in gene expression as they contain binding sites for transcription and regulatory factors. The yeast SUC gene family is a useful model to study the influence that nucleotide exchanges within the promoter regions have on their expression, since (i) these genes, regulated by glucose repression, are differentially transcribed (invertase activity produced by distinct SUC genes may show variations of about 10-fold); and (ii) promoter sequences of SUC3, SUC4, SUC5 and SUC7 are more than 99% homologous, showing only six base exchanges among all of them. Comparison of these nucleotide exchan…

GeneticsGlycoside Hydrolasesbeta-FructofuranosidaseGenes FungalSaccharomyces cerevisiaeNucleic acid sequenceGenetic VariationSaccharomyces cerevisiaeBiologybiology.organism_classificationMicrobiologyInfectious DiseasesPlasmidTranscription (biology)Gene Expression Regulation FungalMultigene FamilyGene expressionGene familyBinding sitePromoter Regions GeneticGeneFEMS Microbiology Reviews
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Isolation of theMNN9gene ofYarrowia lipolytica(YlMNN9) and phenotype analysis of a mutantylmnn9Δ strain

2003

In this work we describe the isolation of the Yarrowia lipolytica homologue of Saccharomyces cerevisiae MNN9 gene, which we have named YlMNN9, and the phenotype analysis of a Y. lipolytica strain containing the disrupted YlMNN9 allele. YlMNN9 was cloned using degenerate consensus oligonucleotides to generate specific probes that were in turn used to screen mini-gene libraries. The gene is defined by a 1014 bp ORF predicted to encode a protein 337 amino acids long that shares significant homology with the Mnn9ps of S. cerevisiae, Candida albicans and Hansenula polymorpha, including a putative N-terminal transmembrane domain. Disruption of YlMNN9 leads to phenotypes such as resistance to sodi…

GeneticsGlycosylationbiologySaccharomyces cerevisiaeMutantBioengineeringYarrowiabiology.organism_classificationApplied Microbiology and BiotechnologyBiochemistryHomology (biology)Transmembrane domainchemistry.chemical_compoundchemistryGeneticsGeneHygromycin BBiotechnologyYeast
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The Conserved Foot Domain of RNA Pol II Associates with Proteins Involved in Transcriptional Initiation and/or Early Elongation

2011

RNA polymerase (pol) II establishes many protein-protein interactions with transcriptional regulators to coordinate different steps of transcription. Although some of these interactions have been well described, little is known about the existence of RNA pol II regions involved in contact with transcriptional regulators. We hypothesize that conserved regions on the surface of RNA pol II contact transcriptional regulators. We identified such an RNA pol II conserved region that includes the majority of the >foot> domain and identified interactions of this region with Mvp1, a protein required for sorting proteins to the vacuole, and Spo14, a phospholipase D. Deletion of MVP1 and SPO14 affects …

GeneticsGuanylyltransferaseChromatin ImmunoprecipitationSequence Homology Amino AcidTranscription GeneticMolecular Sequence DataRNA polymerase IISaccharomyces cerevisiaeInvestigationsBiologyReal-Time Polymerase Chain Reactionchemistry.chemical_compoundchemistryTranscription (biology)Capping enzymeRNA polymeraseGeneticsTranscriptional regulationbiology.proteinAmino Acid SequenceRNA Polymerase IITranscription factor II DGeneConserved SequenceGenetics
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Self-diploidization in Saccharomyces cerevisiae kar2 heterokaryons

1993

Zygotes isolated by micromanipulation from crosses of Saccharomyces cerevisiae strains, one of which carries a kar mutation, give rise most frequently to cytoductant colonies showing the nuclear constitution of either one of the two haploid parental strains. In crosses of kar2-1 strains to wild-type, about 10% of the cytoductants of both mating types are homozygous autodiploids. There is evidence indicating that self-diploidization occurs by fusion between sibling nuclei in the heterokaryotic zygote. Here we describe this phenomenon and propose to take advantage of it for the construction of genotypically-defined diploids able to mate, and of polyploid strains, which are useful tools in gen…

GeneticsHeterokaryonMating typeZygoteGenotypebiologyZygoteGenes FungalSaccharomyces cerevisiaeSaccharomyces cerevisiaeGeneral Medicinebiology.organism_classificationDiploidyKaryogamyPhenotypePolyploidKaryotypingMutationGeneticsMatingPloidyCrosses GeneticCurrent Genetics
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The Sas3p and Gcn5p histone acetyltransferases are recruited to similar genes.

2006

A macroarray platform was used to identify binding sites of yeast histone acetyltransferase catalytic subunits and to correlate their positions with acetylation of lysine 14 of histone H3, revealing that Sas3p and Gcn5p are recruited to similar sets of intensely transcribed genes.

GeneticsHistone AcetyltransferasesChromatin ImmunoprecipitationSaccharomyces cerevisiae ProteinsResearchAcetylationHistone acetyltransferaseSaccharomyces cerevisiaeSAP30BiologyCell biologyHistonesHistone H3GenòmicaHistone H1Histone methyltransferaseGene Expression Regulation FungalHistone H2Abiology.proteinHistone codeHistone Acetyltransferases
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Genomics and the gene transcription kinetics in yeast.

2007

As an adaptive response to new conditions, mRNA concentrations in eukaryotes are readjusted after any environmental change. Although mRNA concentrations can be modified by altering synthesis and/or degradation rates, the rapidity of the transition to a new concentration depends on the regulation of mRNA stability. There are several plausible transcriptional strategies following environmental change, reflecting different degrees of compromise between speed of response and cost of synthesis. The recent development of genomic techniques now enables researchers to determine simultaneously (either directly or indirectly) the transcription rates and mRNA half-lifes, together with mRNA concentrati…

GeneticsMessenger RNAbiologyModels GeneticTranscription GeneticKineticsGene ExpressionGenomicsAdaptive responseGenomicsSaccharomyces cerevisiaebiology.organism_classificationSaccharomycesYeastCell biologyKineticsSaccharomycesGenòmicaTranscripció genèticaTranscription (biology)GeneticsRNA MessengerGeneForecasting
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Rapid characterization of four species of the Saccharomyces sensu stricto complex according to mitochondrial DNA patterns

1994

Several strains of the four sibling species of the genus Saccharomyces (S. bayanus, S. cerevisiae, S. paradoxus, and S. pastorianus) were characterized by using a rapid and simple method of restriction analysis of mitochondrial DNA. Patterns obtained with four-cutter endonucleases (such as AluI, DdeI, HinfI, and RsaI) made it possible to differentiate each species. S. cerevisiae and S. paradoxus presented a greater number of large fragments than S. pastorianus and S. bayanus with all the assay enzymes. With AluI and DdeI, species-specific bands clearly permitted differentiation between S. pastorianus and S. bayanus. To test the resolution of this method, wild Saccharomyces strains were anal…

GeneticsMitochondrial DNAImmunologySaccharomyces cerevisiaeSaccharomyces bayanusBiologySaccharomyces pastorianusbiology.organism_classificationMicrobiologySaccharomycesParadoxusDNA MitochondrialRestriction fragmentSaccharomycesbiology.proteinSaccharomyces paradoxusDNA Fungal
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Interactions between the yeast mitochondrial and nuclear genomes: isogenic suppressive and hypersuppressive petites differ in their resistance to the…

1990

In a previous paper we have shown that the alkaloid lycorine inhibits growth of rho+, mit- and rho-, strains of Saccharomyces cerevisiae, whereas strains devoid of mitochondrial DNA (rho degrees) are resistant to more than 200 micrograms/ml of the alkaloid. In this report we show that hypersuppressive petites are almost as resistant as rho degrees mutants, whereas isogenic rho- petites, which have retained longer segments of the genome, are sensitive to the drug.

GeneticsMitochondrial DNAMutationbiologyAlkaloidSaccharomyces cerevisiaeMutantDrug Resistance MicrobialSaccharomyces cerevisiaeGeneral Medicinebiology.organism_classificationLycorinemedicine.disease_causeDNA MitochondrialMolecular biologyGenomeYeastPhenanthridineschemistry.chemical_compoundchemistryAmaryllidaceae AlkaloidsGeneticsmedicineDNA FungalCurrent Genetics
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The molecular characterization of new types of Saccharomyces cerevisiae × S. kudriavzevii hybrid yeasts unveils a high genetic diversity

2012

New double- and triple-hybrid Saccharomyces yeasts were characterized using PCR-restriction fragment length polymorphism of 35 nuclear genes, located on different chromosome arms, and the sequencing of one nuclear and one mitochondrial gene. Most of these new hybrids were originally isolated from fermentations; however, two of them correspond to clinical and dietary supplement isolates. This is the first time that the presence of double-hybrid S. cerevisiae×S. kudriavzevii in non-fermentative substrates has been reported and investigated. Phylogenetic analysis of the MET6 nuclear gene confirmed the double or triple parental origin of the new hybrids. Restriction analysis of gene regions in …

GeneticsMitochondrial DNANuclear genebiologyPhylogenetic treeSaccharomyces cerevisiaeChromosomeBioengineeringbiology.organism_classificationApplied Microbiology and BiotechnologyBiochemistryGenomeSaccharomycesGeneticsGeneBiotechnologyYeast
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Functional analysis of yeast gene families involved in metabolism of vitamins B1and B6

2002

In order to clarify their physiological functions, we have undertaken a characterization of the three-membered gene families SNZ1-3 and SNO1-3. In media lacking vitamin B(6), SNZ1 and SNO1 were both required for growth in certain conditions, but neither SNZ2, SNZ3, SNO2 nor SNO3 were required. Copies 2 and 3 of the gene products have, in spite of their extremely close sequence similarity, slightly different functions in the cell. We have also found that copies 2 and 3 are activated by the lack of thiamine and that the Snz proteins physically interact with the thiamine biosynthesis Thi5 protein family. Whereas copy 1 is required for conditions in which B(6) is essential for growth, copies 2 …

GeneticsProtein familyFunctional analysisSaccharomyces cerevisiaeBioengineeringMetabolismBiologybiology.organism_classificationApplied Microbiology and BiotechnologyBiochemistrychemistry.chemical_compoundBiochemistryBiosynthesischemistryGeneticsGene familyThiamineGeneBiotechnologyYeast
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