Search results for "OxyR"

showing 10 items of 216 documents

A legacy of contrasting spatial genetic structure on either side of the Atlantic-Mediterranean transition zone in a marine protist

2012

The mechanisms that underpin the varied spatial genetic structures exhibited by free-living marine microorganisms remain controversial, with most studies emphasizing a high dispersal capability that should redistribute genetic diversity in contrast to most macroorganisms whose populations often retain a genetic signature of demographic response to historic climate fluctuations. We quantified the European phylogeographic structure of the marine flagellate Oxyrrhis marina and found a marked difference in spatial genetic structure, population demography, and genetic diversity between the northwest Atlantic and Mediterranean Sea that reflects the persistent separation of these regions as well …

Environmental changePopulationBiologygeneettinen rakenneElectron Transport Complex IVOxyrrhis marinaGenetic variationAnimalseducationAtlantic OceanPhylogenyeducation.field_of_studyGenetic diversityMultidisciplinaryGeographyModels GeneticMediterranean RegionEcologyGenetic VariationBiological Sciencesbiology.organism_classificationOxyrrhis marinaEuropeGenetic divergencePhylogeographyGenetics PopulationHaplotypesGenetic structureDinoflagellidaBiological dispersalta1181spatial genetic structureEnvironmental MonitoringProceedings of the National Academy of Sciences of the United States of America
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Neutral deoxyribonucleases of HeLa S3 cells: electrophoretic separation, characterization, substrate specificity and mode of action.

1980

Extracts of HeLa S3 cells were electrophoresed on polyacrylamide gels; gel slices were eluted and the eluates were assayed for DNase activities against native and denatured DNA substrates in the presence of MgCl2 or Na2EDTA. Aliquots of each eluate were also assayed for their ability to nick the circular supercoiled PM2 phage DNA to distinguish endonucleases from exonucleases. Peaks of endonuclease activities were characterized as forming 3′-phospho-oligonucleotides or 5′-phospho-oligonucleotides by the use of oligonucleotides produced by these enzymes as substrates for the 5′-phosphate-specific snake venom exonuclease. The total activity of DNases in gel eluates was much higher than that i…

ExonucleasePolyacrylamideDNA Single-StrandedBiochemistrySubstrate SpecificityEndonucleasechemistry.chemical_compoundHumansMagnesiumEdetic Acidchemistry.chemical_classificationChromatographyDeoxyribonucleasesbiologyOligonucleotideHydrogen-Ion ConcentrationElectrophoresisEnzymeBiochemistrychemistryDNA Viralbiology.proteinElectrophoresis Polyacrylamide GelDNA CircularDeoxyribonucleasesDNAHeLa CellsEuropean journal of biochemistry
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How Proximal Nucleobases Regulate the Catalytic Activity of G-Quadruplex/Hemin DNAzymes

2018

International audience; G-quadruplexes (G4s) are versatile catalytic DNAs when combined with hemin. Despite the repertoire of catalytically competent G4/hemin complexes studied so far, little is known about the detailed catalytic mechanism of these biocatalysts. Herein, we have carried out an in-depth analysis of the hemin binding site within the G4/hemin catalysts, providing the porphyrinic cofactor with a controlled nucleotidic environment. We intensively assessed the position-dependent catalytic enhancement in model reactions and found that proximal nucleobases enhance the catalytic ability of the G4/hemin complexes. Our results allow for revisiting the mechanism of the G4/hemin-based ca…

G4-based catalystDNAzymeproximal nucleobasesDeoxyribozyme010402 general chemistryG-quadruplex01 natural sciencesCatalysisCofactorCatalysisNucleobasechemistry.chemical_compoundG4/hemin complexpolycyclic compoundsNucleotideheterocyclic compoundsBinding sitechemistry.chemical_classificationbiology010405 organic chemistryG-quartetGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysisequipment and suppliesCombinatorial chemistry0104 chemical scienceschemistrybiology.proteinHemin
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MboII endonuclease heat inactivation before agarose gel electrophoresis to prevent artifactual bands in restriction patterns

1999

Gel electrophoresisDNA BacterialElectrophoresis Agar GelProtein DenaturationSettore MED/07 - Microbiologia E Microbiologia ClinicaHot TemperaturebiologyMolecular biologyGeneral Biochemistry Genetics and Molecular BiologyRestriction fragmentHeat inactivationElectrophoresischemistry.chemical_compoundRestriction enzymeBiochemistrychemistryAgarose gel electrophoresisEnzyme Stabilitybiology.proteinEscherichia coliDeoxyribonucleases Type II Site-SpecificMboII endonucleaseDNAPolymorphism Restriction Fragment LengthBiotechnology
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Autoregulation of NFATc1/A Expression Facilitates Effector T Cells to Escape from Rapid Apoptosis

2002

AbstractThreshold levels of individual NFAT factors appear to be critical for apoptosis induction in effector T cells. In these cells, the short isoform A of NFATc1 is induced to high levels due to the autoregulation of the NFATc1 promoter P1 by NFATs. P1 is located within a CpG island in front of exon 1, represents a DNase I hypersensitive chromatin site, and harbors several sites for binding of inducible transcription factors, including a tandemly arranged NFAT site. A second promoter, P2, before exon 2, is not controlled by NFATs and directs synthesis of the longer NFATc1/B+C isoforms. Contrary to other NFATs, NFATc1/A is unable to promote apoptosis, suggesting that NFATc1/A enhances eff…

Gene isoformTranscription GeneticMolecular Sequence DataImmunologyApoptosisBiologyT-Lymphocytes RegulatoryJurkat CellsMiceExonAnimalsDeoxyribonuclease IHomeostasisHumansImmunology and AllergyPromoter Regions GeneticTranscription factorMice Inbred BALB CBase SequenceNFATC Transcription Factorsintegumentary systemEffectorNuclear ProteinsNFATDNA MethylationMolecular biologyChromatinDNA-Binding ProteinsAlternative SplicingInfectious DiseasesCpG siteApoptosisElectrophoresis Polyacrylamide GelPoly ATranscription FactorsImmunity
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Polymerase chain reaction analysis of the Xba I polymorphism of the human complement C4 genes provides evidence for strong haplotype conservation.

1995

The genes coding for the two isotypes of the fourth component of human complement, C4A and C4B, are located between the HLA-B and -DR loci of the MHC. We studied the linkage relationship of the previously described XbaI RFLP to obtain further insight into the evolution of the tandemly arranged C4 genes. Using exon-specific PCR amplification followed by restriction analysis and direct DNA sequencing, the polymorphic site could be located in exon 40 of the C4 gene (cDNA position 5095). The polymorphism does not change an amino acid residue. Using nested PCR amplification with isotype-specific primers to amplify either C4A or C4B alleles the haplotype arrangement of the XbaI sites in both isot…

Genetic LinkageImmunologyMolecular Sequence DataBiologyPolymerase Chain Reactionlaw.inventionExonlawComplementary DNAImmunology and AllergyHumansDeoxyribonucleases Type II Site-SpecificGenePolymerase chain reactionGeneticsPolymorphism GeneticBase SequenceHaplotypeIntronChromosome MappingComplement C4General MedicineMolecular biologyRestriction siteHaplotypesRestriction fragment length polymorphismPolymorphism Restriction Fragment LengthHuman immunology
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Chromatin structure of yeast genes.

1989

GeneticsDeoxyribonucleasesBioengineeringSaccharomyces cerevisiaeBiologyApplied Microbiology and BiotechnologyBiochemistryChromatin remodelingYeastChromatinChromatinCell biologyHistoneGeneticsbiology.proteinNucleosomeDNA FungalGeneChIA-PETBiotechnologyBivalent chromatinYeast (Chichester, England)
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DNA polymorphism of the human complement C8 beta gene: formal genetics and intragenic localization.

1989

The eighth component of human complement consists of three subunits of different molecular mass, which are coded for by three separate genetic loci. Polymorphisms have been described at the protein level for the alpha and beta subunits by means of sodium dodecyl sulfate gel electrophoresis and isoelectric focusing. Using a full-length human C8 beta cDNA probe, we have studied more than 100 individuals by Southern blot analysis to detect DNA polymorphisms. We have found two restriction fragment length polymorphisms (RFLPs) with the enzymes Taq I and Bam HI. The Taq I polymorphism is defined by two alleles, i.e., a single 4.9 kb fragment or two 2.8/2.1 kb fragments. The allele frequencies are…

GeneticsGel electrophoresisDeoxyribonuclease BamHIImmunologyBiologyMolecular biologyComplement C8Restriction fragmentBlotting SouthernGene mappingComplementary DNAGeneticsbiology.proteinHumansRestriction fragment length polymorphismDeoxyribonucleases Type II Site-SpecificGeneAllele frequencyAllelesPolymorphism Restriction Fragment LengthSouthern blotImmunogenetics
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Nucleotide sequence of a Trichophyton mentagrophytes HindIII mitochondrial DNA fragment containing at RNA gene cluster

1993

A 0.85-kb HindIII mitochondrial DNA fragment of the dermatophytic fungus Trichophyton mentagrophytes has been sequenced. The fragment contains eight complete genes which corresponds to a tRNA gene cluster. From 5′ to 3′, the sequenced genes code for tRNAthr, tRNAglu, tRNAval, tRNAmet1, tRNAmet3, tRNAleu, tRNAala, and tRNAphe. This tRNA gene cluster is located downstream of the larger ribosomal RNA gene. The particularities ofthe sequenced genes and their comparison with other fungal tRNA mitochondrial genes are reported.

GeneticsMitochondrial DNAbiologyNucleic acid sequenceMicrobiologyMolecular biologyHomology (biology)Restriction fragmentGene clusterTransfer RNAGeneticsbiology.proteinDeoxyribonuclease HindIIIMolecular BiologyGeneFEMS Microbiology Letters
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Intragenomic recombination between homologous regions of genes II and IV promotes formation of bacteriophage f1 miniphages.

1987

GeneticsRecombination GeneticBase SequenceGenes ViralDNA Restriction EnzymesBiologybiology.organism_classificationColiphagesVirusHomology (biology)BacteriophageSequence Homology Nucleic AcidGeneticsHomologous chromosomeBase sequenceDeoxyribonucleases Type II Site-SpecificGeneRecombinationNucleic acids research
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