Search results for "Saccharomyce"

showing 10 items of 875 documents

Dynamic modulation of Dnmt2-dependent tRNA methylation by the micronutrient queuine

2015

Dnmt2 enzymes are cytosine-5 methyltransferases that methylate C38 of several tRNAs. We report here that the activities of two Dnmt2 homologs, Pmt1 from Schizosaccharomyces pombe and DnmA from Dictyostelium discoideum, are strongly stimulated by prior queuosine (Q) modification of the substrate tRNA. In vivo tRNA methylation levels were stimulated by growth of cells in queuine-containing medium; in vitro Pmt1 activity was enhanced on Q-containing RNA; and queuine-stimulated in vivo methylation was abrogated by the absence of the enzyme that inserts queuine into tRNA, eukaryotic tRNA-guanine transglycosylase. Global analysis of tRNA methylation in S. pombe showed a striking selectivity of Pm…

RNA Transfer AspTRNA modificationGuanineMethyltransferaseTRNA methylationbiologyQueuosineQueuineMethylationbiology.organism_classificationMethylationchemistry.chemical_compoundRNA TransferchemistryBiochemistrySchizosaccharomycesTransfer RNAGeneticsRNADictyosteliumDNA (Cytosine-5-)-MethyltransferasesMicronutrientsPentosyltransferasesSchizosaccharomyces pombe ProteinsSchizosaccharomycesNucleic Acids Research
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The Dnmt2 RNA methyltransferase homolog of Geobacter sulfurreducens specifically methylates tRNA-Glu

2014

Dnmt2 enzymes are conserved in eukaryotes, where they methylate C38 of tRNA-Asp with high activity. Here, the activity of one of the very few prokaryotic Dnmt2 homologs from Geobacter species (GsDnmt2) was investigated. GsDnmt2 was observed to methylate tRNA-Asp from flies and mice. Unexpectedly, it had only a weak activity toward its matching Geobacter tRNA-Asp, but methylated Geobacter tRNA-Glu with good activity. In agreement with this result, we show that tRNA-Glu is methylated in Geobacter while the methylation is absent in tRNA-Asp. The activities of Dnmt2 enzymes from Homo sapiens, Drosophila melanogaster, Schizosaccharomyces pombe and Dictyostelium discoideum for methylation of the …

RNA Transfer AsptRNA MethyltransferasesMethyltransferasebiologyNucleic Acid EnzymesRNAMethylationbiology.organism_classificationMethylationDictyostelium discoideumRNA Transfer GluSubstrate SpecificityMiceBiochemistryBacterial ProteinsTransfer RNASchizosaccharomyces pombeGeneticsAnimalsHumansNucleic Acid ConformationGeobacterGeobacter sulfurreducensGeobacterNucleic Acids Research
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Strategie microbiologiche per la produzione di vini base ad elevata acidità da racemi della cultivar Grillo per l’ottenimento di spumanti siciliani

Sempre maggiore è l’importanza che stanno acquisendo gli spumanti Italiani nel mondo, ed anche la produzione vitivinicola in Sicilia è aumentata nell’ultimo decennio. Gli spumanti di qualità, però, sono caratterizzati da un’elevata acidità che non sempre è raggiunta nei vini base e negli spumanti prodotti nelle aree con climi caldo-temperati come quello siciliano. A tale scopo, si sono svolte delle fermentazioni su un mosto di racemi di Grillo, per l’ottenimento del vino di base spumante, avviando numerose attività di natura microbiologica, molecolare, chimico-fisica e sensoriale. I lieviti utilizzati come starter nelle fermentazioni, sono stati isolati da uve racemi raccolte nelle vendemmi…

Racemi Saccharomyces cerevisiae spumante
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The yeast putative transcriptional repressor RGM1 is a proline-rich zinc finger protein.

1991

Abstract I have cloned a yeast gene, RGM1, which encodes a proline-rich zinc, finger protein. rgm1 mutants do not show any obvious phenotype but overexpression of RGM1 gene greatly impairs cell growth. The proline-rich region of RGM1 attached to a heterologous DNA binding domain is able to repress the expression of the target gene. RGM1 shares similar zinc finger motifs with the mammalian Egr (early growth response) proteins as well as proline-rich sequences with a high serine and threonine content, suggesting that RGM1 and Egr proteins could have functional similarities.

Recombinant Fusion ProteinsMolecular Sequence DataRestriction MappingGene ExpressionSaccharomyces cerevisiaeBiologyZIC2TransfectionSequence Homology Nucleic AcidGene expressionGeneticsAmino Acid SequenceCloning MolecularLIM domainSIN3BZinc fingerBase SequenceZinc FingersDNA-binding domainZinc finger nucleaseRING finger domainbody regionsRepressor ProteinsBiochemistryMutagenesisCarbohydrate MetabolismPlasmidsNucleic acids research
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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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The Yeast External Invertase as a Reporter to Study Regulation ofCandida Albicans Promoter Sequences inSaccharomyces Cerevisiae

2008

Regulation of gene expressionInvertasebiologySaccharomyces cerevisiaeCandida albicansbiology.organism_classificationYeastMicrobiology
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The transcriptional inhibitor thiolutin blocks mRNA degradation in yeast.

2007

Thiolutin is commonly used as a general inhibitor of transcription in yeast. It has been used to calculate mRNA decay rates by stopping the transcription and then determining the relative abundance of individual mRNAs at different times after inhibition. We report here that thiolutin is also an inhibitor of mRNA degradation, and thus its use can lead to miscalculations of mRNA half-lives. The inhibition of mRNA decay seems to affect the mRNA degradation pathway without impeding poly(A) shortening, given that the decay rate of total poly(A) amount is not reduced by thiolutin. Moreover, the thiolutin-dependent inhibition of mRNA degradation has variable effects on different functional groups …

Regulation of gene expressionMessenger RNARNA StabilityFungal geneticsRNABioengineeringRNA FungalSaccharomyces cerevisiaeBiologyApplied Microbiology and BiotechnologyBiochemistryThiolutinMolecular biologyYeastPyrrolidinonesCell biologyTranscription (biology)Gene Expression Regulation FungalGeneticsmedicineRNA MessengerGeneBiotechnologymedicine.drugYeast (Chichester, England)
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Genomic-Wide Methods to Evaluate Transcription Rates in Yeast

2011

Gene transcription is a dynamic process in which the desired amount of an mRNA is obtained by the equilibrium between its transcription (TR) and degradation (DR) rates. The control mechanism at the RNA polymerase level primarily causes changes in TR. Despite their importance, TRs have been rarely measured. In the yeast Saccharomyces cerevisiae, we have implemented two techniques to evaluate TRs: run-on and chromatin immunoprecipitation of RNA polymerase II. These techniques allow the discrimination of the relative importance of TR and DR in gene regulation for the first time in a eukaryote.

Regulation of gene expressionMessenger RNAbiologySaccharomyces cerevisiaeRNA polymerase IIbiology.organism_classificationYeastCell biologychemistry.chemical_compoundchemistryTranscription (biology)RNA polymerasebiology.proteinChromatin immunoprecipitation
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Respiration and low cAMP-dependent protein kinase activity are required for high-level expression of the peroxisomal thiolase gene in Saccharomyces c…

1996

Transcription of genes for peroxisomal proteins is repressed by glucose and induced by oleate. At least for the peroxisomal thiolase gene (POT1) there is a third regulatory mechanism, mediated by the transcription factor Adr1p, which is responsible for the high-level expression of the gene in stationary phase. Here we show that a region in the POT1 promoter that extends from positions -238 to -152 mediates this mechanism, and we suggest that Adr1p acts indirectly on POT1. We have also analyzed the role of the cAMP-dependent protein kinase (PKA) in the transcriptional regulation of POT1. PKA exerts a negative control: the high, unregulated PKA activity in a bcy1 mutant maintains POT1 transcr…

Regulation of gene expressionSaccharomyces cerevisiae ProteinsTranscription GeneticThiolaseSaccharomyces cerevisiaeBiologyRegulatory Sequences Nucleic AcidCAMP-dependent protein kinase activityCyclic AMP-Dependent Protein KinasesMicrobodiesMitochondriaDNA-Binding ProteinsFungal ProteinsBiochemistryRegulatory sequenceGene Expression Regulation FungalGeneticsTranscriptional regulationRas2Acetyl-CoA C-AcetyltransferaseProtein kinase APromoter Regions GeneticMolecular BiologyTranscription factorTranscription FactorsMoleculargeneral genetics : MGG
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A new Multi-Layers Method to Analyze Gene Expression

2007

In the paper a new Multi-Layers approach (called Multi-Layers Model MLM) for the analysis of stochastic signals and its application to the analysis of gene expression data is presented. It consists in the generation of sub-samples from the input signal by applying a threshold technique based on cut-set optimal conditions. The MLM has been applied on synthetic and real microarray data for the identification of particular regions across DNA called nucleosomes and linkers. Nucleosomes are the fundamental repeating subunits of all eukaryotic chromatin, and their positioning provides useful information regarding the regulation of gene expression in eukaryotic cells. Results have shown a good rec…

Regulation of gene expressionbiologySettore INF/01 - InformaticaComputer scienceMicroarray analysis techniquesSaccharomyces cerevisiaeChromosomeComputational biologybiology.organism_classificationBioinformaticsSynthetic dataBioinformatics Nucleosome positioning Multi layer methods.ChromatinIdentification (information)chemistry.chemical_compoundchemistrySettore BIO/10 - BiochimicaGene expressionNucleosomeHidden Markov modelDNA
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