Search results for "primer"

showing 10 items of 530 documents

A molecular method to assess Phytophthora diversity in environmental samples

2012

Current molecular detection methods for the genus Phytophthora are specific to a few key species rather than the whole genus and this is a recognized weakness of protocols for ecological studies and international plant health legislation. In the present study a molecular approach was developed to detect Phytophthora species in soil and water samples using novel sets of genus-specific primers designed against the internal transcribed spacer (ITS) regions. Two different rDNA primer sets were tested: one assay amplified a long product including the ITS1, 5.8S and ITS2 regions (LP) and the other a shorter product including the ITS1 only (SP). Both assays specifically amplified products from Phy…

Microbiology (medical)PhytophthoraGenus-specific primersRange (biology)Molecular Sequence DataBiodiversityMetagenomic analysesMicrobiologyNatural ecosystemsMicrobial ecologyBotanyDNA Ribosomal SpacerEnvironmental MicrobiologyPythiumInternal transcribed spacerMolecular BiologyMolecular detectionPhytophthora sppDNA PrimersPhylotypebiologyPhytophthora spp.; Molecular detection; Metagenomic analyses; Genus-specific primers; Natural ecosystemsfungifood and beveragesBiodiversitySequence Analysis DNAbiology.organism_classificationClassificationScotlandMetagenomicsPhytophthora
researchProduct

Identification of Shigella sonnei biotype g isolates carrying class 2 integrons in Italy in 2001-2003

2005

ABSTRACT Phenotyping and genotyping have been carried out on 64 epidemic and sporadic isolates of Shigella sonnei identified in Italy in the years 2001 to 2003. Class 2 integron carriage has been also investigated. Isolates from four of the five outbreaks and four of six sporadic cases were biotype g , pulsed-field gel electrophoresis type B, and class 2 integron positive, suggesting emergence and spread of an epidemic clone in Italy.

Microbiology (medical)clone (Java method)Genotypebiotype gSettore MED/42 - Igiene Generale e ApplicataOUTBREAKShigella sonneiIntegronPolymerase Chain Reactionlaw.inventionDisease OutbreaksIntegronslawGenotypeHumansShigella sonneiChildGenotypingPolymerase chain reactionDNA PrimersDysentery BacillaryGeneticsShigella sonnei ; epidemiology ; biotype g ; class 2 integrons ; ItalyRefugeesANTIMICROBIAL RESISTANCEbiologyBase SequenceOutbreakbiochemical phenomena metabolism and nutritionbacterial infections and mycosesclass 2 integronsVirologyElectrophoresis Gel Pulsed-FieldRESTRICTION PATTERNSCarriagePhenotypeItalybiology.proteinbacteriaepidemiology
researchProduct

Hybridization of mouse lemurs: different patterns under different ecological conditions

2011

Abstract Background Several mechanistic models aim to explain the diversification of the multitude of endemic species on Madagascar. The island's biogeographic history probably offered numerous opportunities for secondary contact and subsequent hybridization. Existing diversification models do not consider a possible role of these processes. One key question for a better understanding of their potential importance is how they are influenced by different environmental settings. Here, we characterized a contact zone between two species of mouse lemurs, Microcebus griseorufus and M. murinus, in dry spiny bush and mesic gallery forest that border each other sharply without intermediate habitats…

Microcebus murinusEvolutionMolecular Sequence DataPopulationIntrogressionLemurCheirogaleidaeDNA MitochondrialLinkage DisequilibriumHybrid zonebiology.animalMadagascarQH359-425AnimalseducationEcosystemPhylogenyEcology Evolution Behavior and SystematicsDNA Primerseducation.field_of_studyBase SequenceModels GeneticbiologyEcologyBayes TheoremSequence Analysis DNAbiology.organism_classificationGenetics PopulationHaplotypesHabitatEvolutionary biologyHybridization GeneticCheirogaleidaeMicrocebus griseorufusMicrosatellite RepeatsResearch ArticleBMC Evolutionary Biology
researchProduct

Evolution and genetic structure of the great tit (Parus major) complex

2003

The great tit complex is divided into four groups, each containing several subspecies. Even though the groups are known to differ markedly on morphological, vocal and behavioural characters, some hybridization occurs in the regions where they meet. The great tit has often been referred to as an example of a ring species, although this has later been questioned. Here, we have studied the genetic structure and phylogenetic relationships of the subspecies groups to clarify the evolutionary history of the complex using control region sequences of the mitochondrial DNA. The subspecies groups were found to be monophyletic and clearly distinct in mitochondrial haplotypes, and therefore must have h…

Mitochondrial DNAAsiaZoologySubspeciesBiologyDNA MitochondrialGeneral Biochemistry Genetics and Molecular BiologyEvolution MolecularSongbirdsMonophylyPhylogeneticsAnimalsCluster AnalysisPhylogenyDNA PrimersGeneral Environmental SciencemtDNA control regionParusGeographyGeneral Immunology and MicrobiologyPhylogenetic treeGeneral MedicineLocus Control Regionbiology.organism_classificationEuropeEvolutionary biologyHybridization GeneticGeneral Agricultural and Biological SciencesResearch ArticleRing speciesProceedings of the Royal Society of London. Series B: Biological Sciences
researchProduct

Reliability of mitochondrial DNA in an acanthocephalan: The problem of pseudogenes

2006

The utility of mitochondrial DNA as a molecular marker for evolutionary studies is well recognized. However, several problems can arise when using mitochondrial DNA, one of which is the presence of nuclear mitochondrial pseudogenes, or Numts. Pseudogenes of cytochrome oxidase I were preferentially amplified from Acanthocephalus lucii (Acanthocephala) using a universal PCR approach. To verify the presence and abundance of pseudogenes, length heterogeneity analysis of the PCR fragments was performed. PCR products obtained with universal primers often contained fragments of different sizes. Cloned sequences from universal PCR products nearly always contained sequence abnormalities such as inde…

Mitochondrial DNAGenotypePseudogeneMolecular Sequence DataBiologyDNA MitochondrialPolymerase Chain ReactionAcanthocephalaElectron Transport Complex IVchemistry.chemical_compoundMolecular markerAnimalsIndelPhylogenyDNA PrimersGeneticsBase SequencePhylogenetic treeBiological EvolutionStop codonInfectious DiseaseschemistryCodon usage biasParasitologyNumtPseudogenesInternational Journal for Parasitology
researchProduct

Sequence polymorphism of mitochondrial DNA control region in Japanese.

1998

Sequence polymorphisms of the mitochondrial DNA (mtDNA) control region, hypervariable regions I and II, from 100 unrelated Japanese were determined by PCR amplification and direct sequencing. Sequences of 404 nucleotides for hypervariable region I and 379 nucleotides for region II were obtained. Variable sites (85 and 45) were revealed in region I and region II, respectively, as compared to the reference sequence, and a total of 96 different genetic patterns from both regions I and II were determined. A point mutation heteroplasmy was observed at the ratio of approximately 50:50 from one individual at the sequence position 151 showing a nucleotide transition from C to T. The probability of …

Mitochondrial DNAGenotypeSequence analysisPopulationMolecular Sequence DataBiologyDNA MitochondrialPolymerase Chain ReactionPathology and Forensic MedicineJapanHumansPoint MutationeducationDNA PrimersmtDNA control regionGeneticseducation.field_of_studyPolymorphism GeneticBase SequenceNucleic acid sequenceSequence Analysis DNALocus Control RegionHeteroplasmyHypervariable regionGenetics PopulationGenetic markerLawForensic science international
researchProduct

Single-tube nested quantitative PCR: a rational and sensitive technique for detection of retroviral DNA. Application to RERV-H/HRV-5 and confirmation…

2003

It was reported earlier that a few patients suffering from non-Hodgkin's lymphoma had low amounts of DNA from the so-called fifth human exogenous retrovirus, HRV-5. A sensitive and rational method for large-scale screening for HRV-5 DNA was therefore developed. It is a single-tube nested quantitative PCR (stnQPCR), which uses two functionally isolated primer pairs and one probe target distinct from related endogenous retroviral sequences, yet encompassing known HRV-5 variation, allowing optimal use of sequence conservation. DNA from lymphoma, myeloma, and follicular dendritic cell lines was tested for HRV-5 positivity, as was DNA from whole blood of blood donors, non-Hodgkin's lymphoma and …

Mitochondrial DNAMolecular Sequence DataAntibodies ViralDNA MitochondrialPolymerase Chain ReactionCell LineArthritis RheumatoidRetrovirusProvirusesVirologymedicineAnimalsHumansLupus Erythematosus SystemicbiologyBase SequenceLymphoma Non-HodgkinEndogenous Retrovirusesmedicine.diseasebiology.organism_classificationVirologyLymphomaReal-time polymerase chain reactionRetroviridaeDNA ContaminationEvaluation Studies as TopicDNA Viralbiology.proteinLeukocytes MononuclearRabbitsAntibodyPrimer (molecular biology)Nested polymerase chain reactionJournal of virological methods
researchProduct

Nocturnin in the demosponge Suberites domuncula: a potential circadian clock protein controlling glycogenin synthesis in sponges

2012

Sponges are filter feeders that consume a large amount of energy to allow a controlled filtration of water through their aquiferous canal systems. It has been shown that primmorphs, three-dimensional cell aggregates prepared from the demosponge Suberites domuncula and cultured in vitro , change their morphology depending on the light supply. Upon exposure to light, primmorphs show a faster and stronger increase in DNA, protein and glycogen content compared with primmorphs that remain in the dark. The sponge genome contains nocturnin, a light/dark-controlled clock gene, the protein of which shares a high sequence similarity with the related molecule of higher metazoans. The sponge nocturnin …

Models MolecularAryl hydrocarbon receptor nuclear translocatorGlycogeninPeriod (gene)Circadian clockGene ExpressionBiochemistry03 medical and health sciencesCryptochromeComplementary DNAAnimalsRNA Messenger14. Life underwaterMolecular BiologyDNA PrimersGlycoproteins030304 developmental biology0303 health sciencesBase SequencebiologyCircadian Rhythm Signaling Peptides and Proteins030302 biochemistry & molecular biologyNuclear ProteinsCell Biologybiology.organism_classificationCircadian RhythmSuberites domunculaCLOCKBiochemistryGlucosyltransferasesSuberitesTranscription FactorsBiochem. J.
researchProduct

Asp333, Asp495, and His52.3 Form the Catalytic Triad of Rat Soluble Epoxide Hydrolase

1996

On the basis of the sequence similarity between mammalian epoxide hydrolases and bacterial haloalkane dehalogenase reported earlier (Arand, M., Grant, D. F., Beetham, J. K., Friedberg, T., Oesch, F., and Hammock, B. D. (1994) FEBS Lett. 338, 251-256; Beetham, J. K., Grant, D., Arand, M., Garbarino, J., Kiyosue, T., Pinot, F., Oesch, F., Belknap, W. R., Shinozaki, K., and hammock, B. D. (1995) DNA Cell. Biol. 14, 61-71) we selected candidate amino acid residues for the putative catalytic triad of the rat soluble epoxide hydrolase. The predicted amino acid residues were exchanged by site-directed mutagenesis of the epoxide hydrolase cDNA, followed by the expression of the respective mutant en…

Models MolecularEpoxide hydrolase 2StereochemistryMolecular Sequence DataRestriction MappingPolymerase Chain ReactionBiochemistryCatalysisProtein Structure SecondaryCatalytic triadEscherichia coliAnimalsHumansPoint MutationHistidineAmino Acid SequenceCloning MolecularEpoxide hydrolaseMolecular BiologyPeptide sequenceDNA PrimersEpoxide Hydrolaseschemistry.chemical_classificationAspartic AcidBinding SitesSequence Homology Amino AcidChemistryCell BiologyRecombinant ProteinsRatsAmino acidEpoxide hydrolase activityKineticsBiochemistryEpoxide HydrolasesMutagenesis Site-DirectedHaloalkane dehalogenaseJournal of Biological Chemistry
researchProduct

A Short Caspase-3 Isoform Inhibits Chemotherapy-Induced Apoptosis by Blocking Apoptosome Assembly

2011

Alternative splicing of caspase-3 produces a short isoform caspase-3s that antagonizes caspase-3 apoptotic activity. However, the mechanism of apoptosis inhibition by caspase-3s remains unknown. Here we show that exogenous caspase-3 sensitizes MCF-7 and HBL100 breast cancers cells to chemotherapeutic treatments such as etoposide and methotrexate whereas co-transfection with caspase-3s strongly inhibits etoposide and methotrexate-induced apoptosis underlying thus the anti-apoptotic role of caspase-3s. In caspase-3 transfected cells, lamin-A and α-fodrin were cleaved when caspase-3 was activated by etoposide or methotrexate. When caspase-3s was co-transfected, this cleavage was strongly reduc…

Models MolecularImmunoprecipitationScienceBlotting WesternMolecular Sequence DataGene ExpressionApoptosisBreast NeoplasmsCaspase 3BiologyReal-Time Polymerase Chain ReactionBiochemistryRNA interferenceApoptosomesCell Line TumorMolecular Cell BiologyBreast CancermedicineHumansAmino Acid SequenceBiologyEtoposideDNA PrimersMultidisciplinaryCell DeathBase SequenceSequence Homology Amino AcidCaspase 3QRObstetrics and GynecologyTransfectionApoptosome assemblyMolecular biologyEnzymesEnzyme ActivationIsoenzymesApoptosisCancer researchMedicineApoptosomeResearch Articlemedicine.drugPLoS ONE
researchProduct