Search results for "specificity"

showing 10 items of 2234 documents

Midgut aminopeptidase N isoforms from Ostrinia nubilalis: Activity characterization and differential binding to Cry1Ab and Cry1Fa proteins from Bacil…

2013

Aminopeptidase N (APN) isoforms from Lepidoptera are known for their involvement in the mode of action of insecticidal Cry proteins from Bacillus thuringiensis. These enzymes belong to a protein family with at least eight different members that are expressed simultaneously in the midgut of lepidopteran larvae. Here, we focus on the characterization of the APNs from Ostrinia nubilalis (OnAPNs) to identify potential Cry receptors. We expressed OnAPNs in insect cells using a baculovirus system and analyzed their enzymatic activity by probing substrate specificity and inhibitor susceptibility. The interaction with Cry1Ab and Cry1Fa proteins (both found in transgenic insect-resistant maize) was …

Gene isoformendocrine systemCD13 AntigensMothsBiochemistrySubstrate SpecificityOstriniaHemolysin ProteinsBacterial ProteinsBacillus thuringiensisToxicity TestsSf9 CellsAnimalsReceptorMolecular Biologychemistry.chemical_classificationBacillus thuringiensis ToxinsbiologyfungiMidgutbiology.organism_classificationLigand (biochemistry)Molecular biologyEndotoxinsGastrointestinal TractIsoenzymesBlotEnzymechemistryBiochemistryInsect ScienceProtein BindingInsect Biochemistry and Molecular Biology
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Multicenter evaluation of a second-generation assay for cardiac troponin T.

1997

Abstract We report on the evaluation of the second-generation assay for cardiac troponin T (cTnT) on the Enzymun®system. This new assay is completely specific for the cardiac isoform of TnT, utilizing two cardiospecific monoclonal antibodies. The assay time is reduced to 45 min. The interassay precision shows a median CV of 5.5%; 20% interassay CV was found between 0.05 and 0.1 μg/L. The cardiosensitivity of the second-generation cTnT assay in patients with ischemic myocardial injury appears equivalent when compared with the first-generation assay. We found no falsely positive results in patients with skeletal muscle damage including multitraumas, surgery patients, and marathon runners who …

Gene isoformmedicine.medical_specialtyCardiac troponinHeart diseasemedicine.drug_classClinical BiochemistryMyocardial IschemiaMonoclonal antibodySensitivity and SpecificityTroponin complexTroponin TInternal medicinemedicineHumansMuscle SkeletalbiologyTroponin Tbusiness.industryMyocardiumBiochemistry (medical)Skeletal muscleReproducibility of Resultsmedicine.diseaseTroponinTroponinmedicine.anatomical_structureEndocrinologyCardiologybiology.proteinbusinessArtifactsTroponin CBiomarkersClinical chemistry
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Claudin-18 gene structure, regulation, and expression is evolutionary conserved in mammals

2011

Claudin-18 isoform 2 (CLDN18.2) is one of the few members of the human claudin family of tight junction molecules with strict restriction to one cell lineage. The objective of the current study was to compare molecular structure and tissue distribution of this gastrocyte specific molecule in mammals. We show here that the CLDN18.2 protein sequence is highly conserved, in particular with regard to functionally relevant domains in mouse, rat, rabbit, dog, monkey and human and also in lizards. Moreover, promoter regions of orthologs are highly homologous, including the binding site of the transcription factor cyclic AMP-responsive element binding protein (CREB), which is known to regulate acti…

Gene isoformmiceMolecular Sequence DataGene Expressionmolecular structureMammals/geneticsBiologyphylogenyRATSConserved sequenceEvolution MolecularDogsProtein Isoforms/geneticsSequence Homology Nucleic AcidGene expressionGeneticsProtein IsoformsAnimalsTissue DistributionAmino Acid SequenceMembrane Proteins/geneticsBinding sitePromoter Regions GeneticClaudinGeneTranscription factorConserved SequenceGastric Mucosa/metabolismMammalsRegulation of gene expressionGeneticsBinding SitesBase SequenceStomachStomach/cytologyMembrane ProteinsCREB-Binding Protein/metabolismHaplorhiniGeneral MedicineCREB-Binding ProteinGene Expression RegulationGastric MucosaOrgan SpecificityMultigene FamilyClaudinsRabbitsGene
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Identification of pathogenic yeast species by polymerase chain reaction amplification of the RPS0 gene intron fragment.

2009

Aims: This work focuses on the development of a method for the identification of pathogenic yeast. With this aim, we target the nucleotide sequence of the RPS0 gene of pathogenic yeast species with specific PCR primers. PCR analysis was performed with both the genomic DNA, whole cells of clinical isolates of Candida species and clinical samples. Methods and Results: A single pairs of primers, deduced from the nucleotide sequence of the RPS0 gene from pathogenic yeast, were used in PCR analysis performed with both the genomic DNA and whole cells of clinical isolates of Candida species and clinical samples. The primers designed are highly specific for their respective species and produce ampl…

Genes FungalMolecular Sequence DataBiologyApplied Microbiology and BiotechnologyPolymerase Chain ReactionSensitivity and Specificitylaw.inventionchemistry.chemical_compoundSpecies SpecificitylawHumansAmino Acid SequenceDNA FungalGenePolymerase chain reactionCandidaDNA PrimersGeneticsIntronNucleic acid sequenceGeneral MedicineAmpliconYeastIntronsgenomic DNAchemistryDNABiotechnologyJournal of applied microbiology
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Contribution of insertions and deletions to the variability of hepatitis C virus populations

2007

Little is known about the potential effects of insertions and deletions (indels) on the evolutionary dynamics of hepatitis C virus (HCV). In fact, the consequences of indels on antiviral treatment response are a field of investigation completely unexplored. Here, an extensive sequencing project was undertaken by cloning and sequencing serum samples from 25 patients infected with HCV subtype 1a and 48 patients with subtype 1b. For 23 patients, samples obtained after treatment with alpha interferon plus ribavirin were also available. Two genome fragments containing the hypervariable regions in the envelope 2 glycoprotein and the PKR-BD domain in NS5A were sequenced, yielding almost 16 000 seq…

Genes ViralHepatitis C virusMolecular Sequence DataAlpha interferonHepacivirusViral quasispeciesViral Nonstructural ProteinsBiologymedicine.disease_causeAntiviral AgentsGenomeVirusSpecies SpecificityViral Envelope ProteinsVirologyRibavirinmedicineHumansAmino Acid SequenceNS5AIndelGeneticsInterferon-alphavirus diseasesHepatitis CVirologyHypervariable regionMutagenesis InsertionalSpainDrug Therapy CombinationSequence AlignmentGene DeletionJournal of General Virology
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MGFM: a novel tool for detection of tissue and cell specific marker genes from microarray gene expression data

2015

Background Identification of marker genes associated with a specific tissue/cell type is a fundamental challenge in genetic and cell research. Marker genes are of great importance for determining cell identity, and for understanding tissue specific gene function and the molecular mechanisms underlying complex diseases. Results We have developed a new bioinformatics tool called MGFM (Marker Gene Finder in Microarray data) to predict marker genes from microarray gene expression data. Marker genes are identified through the grouping of samples of the same type with similar marker gene expression levels. We verified our approach using two microarray data sets from the NCBI’s Gene Expression Omn…

Genetic MarkersCancer ResearchMicroarraysBiologyMarker genesWeb BrowserProteomicsMarker geneBioconductorGeneticsGeneGenetic Association StudiesGeneticsMicroarray analysis techniquesMethodology ArticleGene Expression ProfilingComputational BiologyReproducibility of Results3. Good healthGene expression profilingSamplesGene OntologyGenetic markerOrgan SpecificityDNA microarrayBiotechnologyBMC Genomics
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Chromosomal variation and genome size support existence of cryptic species of Triatoma dimidiata with different epidemiological importance as Chagas …

2006

Summary The wide geographical distribution of Triatoma dimidiata, one of the three major vectors of Chagas disease, ranges from Mexico to northern Peru. Since this species occupies a great diversity of artificial and natural ecotopes, its eradication is extremely difficult. In order to assist control efforts, we used chromosome analyses and DNA amount as taxonomic markers to study genetic variability in populations of T. dimidiata from Mexico, Guatemala, El Salvador and Colombia. We differentiated three groups or cytotypes defined by characteristic chromosome C-banding patterns and genome size measured by flow cytometry. The three cytotypes are restricted to different geographic locations. …

Genetic MarkersChagas diseaseSpecies complexGenome InsectColombiaChromosomesSpecies SpecificityEl SalvadormedicineAnimalsHumansChagas DiseaseTriatomaTriatoma dimidiataMexicoGenome sizebiologyPublic Health Environmental and Occupational HealthGenetic VariationForestryFlow CytometryGuatemalabiology.organism_classificationmedicine.diseaseInsect VectorsInfectious DiseasesKaryotypingTriatomaParasitologyTropical Medicine and International Health
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Interest of exome sequencing trio-like strategy based on pooled parental DNA for diagnosis and translational research in rare diseases.

2021

Abstract Background Exome sequencing (ES) has become the most powerful and cost‐effective molecular tool for deciphering rare diseases with a diagnostic yield approaching 30%–40% in solo‐ES and 50% in trio‐ES. We applied an innovative parental DNA pooling method to reduce the parental sequencing cost while maintaining the diagnostic yield of trio‐ES. Methods We pooled six (Agilent‐CRE‐v2–100X) or five parental DNA (TWIST‐HCE–70X) aiming to detect allelic balance around 8–10% for heterozygous status. The strategies were applied as second‐tier (74 individuals after negative solo‐ES) and first‐tier approaches (324 individuals without previous ES). Results The allelic balance of parental‐pool v…

Genetic MarkersCost effectivenessTranslational researchBiologyQH426-470Sensitivity and SpecificityWorkflowTranslational Research Biomedicalchemistry.chemical_compoundsymbols.namesakeExome SequencingFalse positive paradoxGeneticsHumansDna poolingGenetic Predisposition to DiseaseGenetic TestingAlleleMolecular BiologyGenetics (clinical)Exome sequencingtrio‐like strategy; parental‐pool strategyGeneticsSanger sequencingcost effectivenessReproducibility of Resultsrare diseasesSequence Analysis DNAOriginal ArticleschemistryResearch DesignsymbolsOriginal ArticleDNAGenome-Wide Association StudyMolecular geneticsgenomic medicine
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Molecular Characterization of a Chromosomal Rearrangement Involved in the Adaptive Evolution of Yeast Strains

2002

Wine yeast strains show a high level of chromosome length polymorphism. This polymorphism is mainly generated by illegitimate recombination mediated by Ty transposons or subtelomeric repeated sequences. We have found, however, that the SSU1-R allele, which confers sulfite resistance to yeast cells, is the product of a reciprocal translocation between chromosomes VIII and XVI due to unequal crossing-over mediated by microhomology between very short sequences on the 5' upstream regions of the SSU1 and ECM34 genes. We also show that this translocation is only present in wine yeast strains, suggesting that the use for millennia of sulfite as a preservative in wine production could have favored …

Genetic MarkersSaccharomyces cerevisiae ProteinsLetterChromosomal rearrangementsAnion Transport ProteinsGenes FungalMolecular Sequence DataSaccharomyces cerevisiaeSaccharomyces cerevisiaeChromosomal rearrangementSaccharomycesGenètica molecularTranslocation GeneticEvolution MolecularSaccharomycesGene FrequencySpecies SpecificityGeneticsVinificationDNA FungalGeneGenetics (clinical)Wine yeastsGene RearrangementRecombination GeneticGeneticsBase SequencebiologyGene rearrangementbiology.organism_classificationYeastYeast in winemakingChromosomes FungalGenome FungalPloidyGenome Research
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Multiplex PCR for species discrimination of Sclerotiniaceae by novel laccase introns

2006

Common PCR-based targets for the identification of filamentous fungi and yeasts are the sequences of the internal transcribed spacer region (ITS1, 5.8S rDNA, ITS2). Within the Sclerotiniaceae the ITS-region is homogenous and the identification is almost impossible. Furthermore, the lack of IGS-data (intergenic spacer region) requires new specific marker genes for a rapid identification of phytopathogenic Sclerotiniaceae. We sequenced and analyzed new laccase2 (lcc2) genes from the phylogenetically related Sclerotinia sclerotiorum (Lib.) de Bary, Sclerotinia minor Jagger, and Monilinia fructigena Honey. Comparative analysis revealed remarkable differences in length and sequence compared to t…

Genetic MarkersSequence analysisGenes FungalMolecular Sequence DataPolymerase Chain ReactionSensitivity and SpecificityMicrobiologyMicrobiologySclerotinia minorAscomycotaSpecies SpecificityDNA Ribosomal SpacerMultiplex polymerase chain reactionSclerotiniaceaeAmino Acid SequenceInternal transcribed spacerDNA FungalMycological Typing TechniquesPhylogenyCandidaMonilinia fructigenaBase SequencebiologyLaccaseSclerotinia sclerotiorumFungal geneticsSequence Analysis DNAGeneral Medicinebiology.organism_classificationIntronsFood MicrobiologyBotrytisFood ScienceInternational Journal of Food Microbiology
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