Search results for "DNA-Directed RNA Polymerases"

showing 10 items of 30 documents

Inhibition of in vitro reconstitution of rotavirus transcriptionally active particles by anti-VP6 monoclonal antibodies

1994

International audience; Six monoclonal antibodies specific for the major capsid protein of rotavirus, VP6, previously characterized, were tested in a biological assay for their capacity to block the transcriptase activity associated with the single-shelled particles. The results showed that two MAbs (RV-50 and RV-133), specific for distinct antigenic sites, were able to block the transcription when they were incubated with a purified baculovirus-expressed group A VP6, prior to the reconstitution of the single-shelled particles from the cores, suggesting that at least two domains are involved in active single-shelled particle reconstitution. The results obtained previously from immunochemist…

RotavirusTranscription Geneticmedicine.drug_classvirusesBiologyMothsMonoclonal antibodymedicine.disease_causeTransfectionAntiviral AgentsCell Line03 medical and health sciencesCapsidAntigenTranscription (biology)VirologyRotavirusImmunochemistrymedicineAnimalsRNA MessengerAntigens Viral030304 developmental biology0303 health sciences030306 microbiologyAntibodies MonoclonalBiological activityRNA-Directed DNA PolymeraseGeneral MedicineDNA-Directed RNA PolymerasesBIOLOGIE MOLECULAIREChromatography Ion ExchangeVirologyMolecular biologyIn vitro3. Good healthVIROLOGIECapsid[SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/VirologyChromatography GelCapsid ProteinsBaculoviridae
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In vitro reconstitution of rotavirus transcriptional activity using viral cores and recombinant baculovirus expressed VP 6

1993

International audience; Purified baculovirus-expressed group A rotavirus VP6 polypeptide was shown to be active in the recovery of the transcriptase activity associated with the reconstitution of the single-shelled rotavirus particle. Recombinant VP6 polypeptide was able to restore the transcriptional activity in purified viral cores from both SA-11 and RF rotavirus strains. Recombinant group C VP 6 (Cowden strain) is capable of binding as a trimer to group A viral core particles but unable to restore the transcriptase activity, suggesting that the binding of the polypeptide to cores is not the only requirement to restore the transcriptase activity. The VP 6 group A polypeptide was shown to…

RotaviruspolypeptidereplicationTranscription Genetic[SDV]Life Sciences [q-bio]virusesReoviridaeimmunogenicitymedicine.disease_causeViruslaw.inventionCapsidsingle-shelled particlelawVirologyRotavirusGene expressionmedicinebovine rotavirusAntigens ViralPolymerasebiologyViral Core Proteinsvirus diseasesDNA-Directed RNA PolymerasesGeneral Medicinebiology.organism_classificationNucleotidyltransferaseVirologyMolecular biologyRecombinant ProteinsIn vitro[SDV] Life Sciences [q-bio]biology.proteinRecombinant DNACapsid ProteinsElectrophoresis Polyacrylamide GelproteinBaculoviridaeArchives of Virology
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Identification of the novel Kawasaki 2014 GII.17 human norovirus strain in Italy, 2015

2015

Surveillance of noroviruses in Italy identified the novel GII.17 human norovirus strain, Kawasaki 2014, in February 2015. This novel strain emerged as a major cause of gastroenteritis in Asia during 2014/15, replacing the pandemic GII.4 norovirus strain Sydney 2012, but being reported only sporadically elsewhere. This novel strain is undergoing fast diversification and continuous monitoring is important to understand the evolution of noroviruses and to implement the future strategies on norovirus vaccines.

Settore MED/07 - Microbiologia E Microbiologia ClinicaGenotypeEpidemiologyvirusesBiologymedicine.disease_causeCommunicable Diseases EmergingMicrobiologyDisease OutbreaksEpidemiology; Public Health Environmental and Occupational Health; Virologyfluids and secretionsVirologyPandemicmedicineHumansPhylogenyCaliciviridae InfectionsMolecular EpidemiologyMolecular epidemiologyStrain (biology)NorovirusPublic Health Environmental and Occupational Healthvirus diseasesGenetic VariationDNA-Directed RNA PolymerasesVirologydigestive system diseasesGastroenteritisCaliciviridae InfectionsItalyPopulation SurveillanceNorovirusFemaleSeasonsSequence Analysis
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The complete genome sequence of Lamium mild mosaic virus, a member of the genus Fabavirus

2013

Springer-Verlag Wien 2013 Abstract Lamium mild mosaic virus (LMMV) is the only one of the five members of the genus Fabavirus for which there are no nucleotide sequence data. In this study, the complete genome sequence of LMMV was determined and compared with the available complete genome sequences of other members of the genus Fabavirus. The genome was the largest of the genus but maintained the typical orga- nization, with RNA 1 of 6080 nucleotides (nt), RNA 2 of 4065 nt, and an unusually long 3 0 untranslated region in RNA 2 of 603 nt. Phylogenetic analysis of the amino acid sequences of the protease-polymerase (Pro-Pol) region and the two coat proteins confirmed that LMMV belongs to a d…

SubfamilyLMMVMolecular Sequence DataGenome ViralGenomeFabaviruBroad bean wilt virusViral ProteinsSpecies SpecificityGenusMosaic VirusesVirologySecoviridaeTobaccoComovirinaePhylogenyPlant DiseasesGeneticsWhole genome sequencingLamiaceaebiologyBase SequenceNucleic acid sequenceSettore AGR/12 - Patologia Vegetalefood and beveragesGeneral MedicineDNA-Directed RNA PolymerasesSequence Analysis DNAClassificationbiology.organism_classificationVirologyFabavirusRNA ViralCapsid ProteinsPeptide Hydrolases
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Superparamagnetic γ-Fe2O3 nanoparticles with tailored functionality for protein separation

2007

Polymer coated superparamagnetic gamma-Fe(2)O(3) nanoparticles were derivatized with a synthetic double-stranded RNA [poly(IC)], a known allosteric activator of the latent (2-5)A synthetase, to separate a single 35 kDa protein from a crude extract which cross reacted with antibodies raised against the sponge enzyme.

Surface PropertiesAllosteric regulationNanoparticleLigandsFerric CompoundsCatalysisMagneticsProtein purification2'5'-Oligoadenylate SynthetaseMaterials ChemistryAnimalsParticle Sizechemistry.chemical_classificationBinding SitesMolecular StructurebiologyImmunomagnetic SeparationMetals and AlloysRNADNA-Directed RNA PolymerasesGeneral ChemistryPolymerbiology.organism_classificationPoriferaSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSpongeEnzymeBiochemistrychemistryCeramics and CompositesNanoparticlesPeptidesSuperparamagnetismChemical Communications
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Measuring RNA polymerase activity genome-wide with high-resolution run-on-based methods

2019

The biogenesis of RNAs is a multi-layered and highly regulated process that involves a diverse set of players acting in an orchestrated manner throughout the transcription cycle. Transcription initiation, elongation and termination factors act on RNA polymerases to modulate their movement along the DNA template in a very precise manner, more complex than previously anticipated. Genome-scale run-on-based methodologies have been developed to study in detail the position of transcriptionally-engaged RNA polymerases. Genomic run-on (GRO), and its many variants and refinements made over the years, are helping the community to address an increasing amount of scientific questions, spanning an incr…

Transcription GeneticComputational biologyGenomeGeneral Biochemistry Genetics and Molecular BiologyDNA sequencing03 medical and health scienceschemistry.chemical_compoundTranscription (biology)RNA polymeraseAnimalsHumansMolecular BiologyPolymerase030304 developmental biology0303 health sciencesbiologySequence Analysis RNA030302 biochemistry & molecular biologyEukaryotaHigh-Throughput Nucleotide SequencingRNADNA-Directed RNA PolymerasesChromatinchemistrybiology.proteinRNABiogenesisMethods
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New insights into the regulatory mechanisms of ppGpp and DksA on Escherichia coli RNA polymerase-promoter complex

2015

The stringent response modulators, guanosine tetraphosphate (ppGpp) and protein DksA, bind RNA polymerase (RNAP) and regulate gene expression to adapt bacteria to different environmental conditions. Here, we use Atomic Force Microscopy and in vitro transcription assays to study the effects of these modulators on the conformation and stability of the open promoter complex (RPo) formed at the rrnA P1, rrnB P1, its discriminator (dis) variant and lambda pR promoters. In the absence of modulators, RPo formed at these promoters show different extents of DNA wrapping which correlate with the position of UP elements. Addition of the modulators affects both DNA wrapping and RPo stability in a promo…

Transcription GeneticStringent responsemedicine.disease_causechemistry.chemical_compoundStructural BiologyRNA polymeraseGene expressionNucleotiderRNAPromoter Regions GeneticTranscription Initiation GeneticRibonucleotides/metabolismchemistry.chemical_classification0303 health sciencesDNA Bacterial/chemistry/ultrastructureEscherichia coli Proteins030302 biochemistry & molecular biologyBacterialEscherichia coli Proteins/metabolismDNA-Directed RNA PolymerasesBiological SciencesBacteriophage lambdaCell biologyEscherichia coli/enzymology/geneticsTranscriptionTranscription InitiationDNA BacterialGuanosine TetraphosphateBiologyPromoter Regions03 medical and health sciencesGeneticInformation and Computing SciencesmedicineGeneticsEscherichia coliEscherichia coli030304 developmental biologyPromoterGenes rRNADNAGene Expression Regulation BacterialRibonucleotidesequipment and suppliesMolecular biologyGuanosine TetraphosphateBacteriophage lambda/geneticschemistryGene Expression RegulationGenesbacteriaDNA-Directed RNA Polymerases/metabolismDNAEnvironmental SciencesGuanosine Tetraphosphate/metabolismDevelopmental Biology//purl.org/pe-repo/ocde/ford#1.06.07 [https]
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The Mu1 transposable element of maize contains two promoter signals recognized by the Escherichia coli RNA polymerase.

1990

The galactokinase (GalK) expression plasmid vector system pKO-1 has been used to screen for promoter elements in the maize transposable element Mu1 that function in Escherichia coli. Two transcriptional start points, named S1 and S2, were identified, which are located in the two direct repeats of the transposable element. This paper demonstrates that sequence elements exist in a plant transposable element which function as prokaryotic promotors.

Transposable elementTranscription GeneticMolecular Sequence DataRestriction MappingBiologymedicine.disease_causeZea mayschemistry.chemical_compoundRNA polymeraseGeneticsmedicineEscherichia coliDirect repeatInsertion sequenceCloning MolecularPromoter Regions GeneticMolecular BiologyEscherichia coliGeneticsExpression vectorBase SequencePromoterDNA-Directed RNA PolymerasesGalactokinasechemistryDNA Transposable ElementsMoleculargeneral genetics : MGG
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Extensive nuclear gyration and pervasive non-genic transcription during primordial germ cell development in zebrafish.

2020

ABSTRACT Primordial germ cells (PGCs) are the precursors of germ cells, which migrate to the genital ridge during early development. Relatively little is known about PGCs after their migration. We studied this post-migratory stage using microscopy and sequencing techniques, and found that many PGC-specific genes, including genes known to induce PGC fate in the mouse, are only activated several days after migration. At this same time point, PGC nuclei become extremely gyrated, displaying general broad opening of chromatin and high levels of intergenic transcription. This is accompanied by changes in nuage morphology, expression of large loci (PGC-expressed non-coding RNA loci, PERLs) that ar…

endocrine systemRNA UntranslatedTranscription GeneticZygotePiwi-interacting RNApiRNABiology03 medical and health sciences0302 clinical medicineGyrationTranscription (biology)Primordial germ cellmedicineAnimalsRNA Small InterferingMolecular BiologyZebrafishGeneZebrafish030304 developmental biologyCell NucleusNuage0303 health sciencesGonadal ridgeurogenital systemNuclear morphologyGene Expression Regulation DevelopmentalDNA-Directed RNA PolymerasesZygotic activationZebrafish Proteinsbiology.organism_classificationChromatinCell biologyUp-Regulationmedicine.anatomical_structureGerm CellsGenetic Loci207FertilizationMutationIntergenic transcriptionDNA Transposable ElementsDNA Intergenic030217 neurology & neurosurgeryGerm cellBiogenesisDevelopmental BiologyResearch ArticleDevelopment (Cambridge, England)
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Biochemical and structural analysis of the NS5B RNA-dependent RNA polymerase of the hepatitis C virus.

2000

Hepatitis C virus (HCV), the major causative agent of chronic and sporadic non-A, non-B hepatitis worldwide, is a distinct member of the Flaviviridae virus family. These viruses have in common a plus-strand RNA genome that is replicated in the cytoplasm of the infected cell via minus-strand RNA intermediates. Owing to the lack of reliable cell culture systems and convenient animal models for HCV, the mechanisms governing RNA replication are not known. As a first step towards the development of appropriate in vitro systems, we expressed the NS5B RNA-dependent RNA polymerase (RdRp) in insect cells, purified the protein to near homogeneity and studied its biochemical properties. It is a primer…

virusesHepatitis C virusGenetic VectorsRNA-dependent RNA polymeraseHepacivirusViral Nonstructural Proteinsmedicine.disease_causeCell LineSubstrate Specificitychemistry.chemical_compoundTranscription (biology)Sequence Analysis ProteinVirologyRNA polymeraseRibavirinmedicineHumansNS5BPolymeraseHepatologybiologyRNANucleosidesDNA-Directed RNA PolymerasesRNA-Dependent RNA PolymeraseVirologyRecombinant ProteinsNS2-3 proteaseInfectious DiseaseschemistryMutationbiology.proteinRNABaculoviridaeJournal of viral hepatitis
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