Search results for "PRIMERS"

showing 10 items of 332 documents

The gene encoding the transcriptional repressor BERF-1 maps to a region of conserved synteny on mouse chromosome 16 and human chromosome 3 and a rela…

1999

We have recently identified and characterized a Kruppel-like zinc finger protein (BERF-1), that functions as a repressor of β enolase gene transcription. By interspecific backcross analysis the gene encoding BERF-1 was localized 4.7 cM proximal to the <i>Mtv6</i> locus on mouse chromosome 16, and an isolated pseudogene was localized to mouse chromosome 8, about 5.3 cM distal to the D8Mit4 marker. Nucleotide sequence identity and chomosome location indicate that the gene encoding BERF-1 is the mouse homologue (<i>Zfp148</i>) of ZNF148 localized to human chromosome 3q21, a common translocation site in acute myeloid leukemia patients.

Genetic MarkersDNA ComplementaryTranscription GeneticKruppel-Like Transcription FactorsBiologyHybrid CellsPolymerase Chain ReactionGene Expression Regulation EnzymologicMiceChromosome 16GeneticsAnimalsHumansMolecular BiologyGenetics (clinical)Conserved SequenceSyntenyDNA PrimersGeneticsBase SequenceYY1Chromosome MappingTAF9Zinc FingersTCF4DNA-Binding ProteinsRepressor ProteinsChromosome 3GATAD2BPhosphopyruvate Hydratasecardiovascular systemChromosomes Human Pair 3Chromosome 22PseudogenesTranscription FactorsCytogenetics and cell genetics
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Molecular Characterization of Fusarium oxysporum f. melongenae by ISSR and RAPD Markers on Eggplant

2010

Fusarium oxysporum f. melongenae is a major soil-borne pathogen of eggplant (Solanum melongena). ISSR and RAPD markers were used to characterize Fusarium oxysporum f. melongenae isolates collected from eggplant fields in southern Turkey. Those isolates were not pathogenic to tomato. Pathogens were identified by their morphology, and their identity was confirmed by PCR amplifi- cation using the specific primer PF02-3. The isolates were classified into groups on the basis of ISSR and RAPD fingerprints, which showed a level of genetic speci- ficity and diversity not previously identified in Fusarium oxysporum f. melongenae, suggesting that genetic differences are related to the pathogen in the…

Genetic MarkersFusariumVeterinary medicineSettore BIO/11 - Biologia MolecolareMinisatellite RepeatsMolecular markerBiochemistryFusarium molecular marker virulence genetic differencechemistry.chemical_compoundFusariumMolecular markerBotanyGenetic variationFusarium oxysporumGeneticsSolanum melongenaDNA FungalMolecular BiologyEcology Evolution Behavior and SystematicsDNA PrimersVirulencebiologyGenetic Variationfood and beveragesGeneral Medicinebiology.organism_classificationRandom Amplified Polymorphic DNA TechniqueRAPDGenetic differencechemistryGenetic markerSettore BIO/03 - Botanica Ambientale E ApplicataMicrosatelliteSolanumBiochemical Genetics
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Forensic animal DNA typing: Allele nomenclature and standardization of 14 feline STR markers

2014

Since the domestic cat (Felis catus) has become one of the most popular pets and owners usually develop a close relationship to their cats, it is necessary to take traces of cats into account for forensic casework. For this purpose feline short tandem (STR) repeat markers have been investigated in several earlier studies, but no detailed description of sequence data, allelic variations or a repeat-based nomenclature is available. The aim of the study was to provide a suggestion for the allele nomenclature of 14 cat STR markers according to the recommendations of the International Society for Forensic Genetics (ISFG) for human DNA typing and to present a standardized system for a secure DNA …

Genetic MarkersGeneticsBase SequenceSTR multiplex systemElectrophoresis CapillaryDNABiologyPolymerase Chain ReactionPathology and Forensic Medicinechemistry.chemical_compoundVariable number tandem repeatchemistryTerminology as TopicCatsGeneticsAnimalsTypingAlleleRepeated sequenceNomenclatureAllele frequencyAllelesDNADNA PrimersMicrosatellite RepeatsForensic Science International: Genetics
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Mutations in the β-tropomyosin (TPM2) gene – a rare cause of nemaline myopathy

2002

Nemaline myopathy is a clinically and genetically heterogeneous muscle disorder. In the nebulin gene we have detected a number of autosomal recessive mutations. Both autosomal dominant and recessive mutations have been detected in the genes for alpha -actin and alpha -tropomyosin 3. A recessive mutation causing nemaline myopathy among the Old Order Amish has recently been identified in the gene for slow skeletal muscle troponin T. As linkage studies had shown that at least one further gene exists for nemaline myopathy, we investigated another tropomyosin gene expressed in skeletal muscle, the beta -tropomyosin 2 gene. Screening 66 unrelated patients, using single strand conformation polymor…

Genetic MarkersMaleGenetic LinkageProtein ConformationBiopsyMolecular Sequence DataMutation MissenseTropomyosinmacromolecular substancesMuscle disorderMyopathies NemalineTPM203 medical and health sciencesNebulin0302 clinical medicineNemaline myopathymedicineAnimalsHumansAmino Acid SequenceMuscle SkeletalNemaline bodiesPolymorphism Single-Stranded ConformationalGenetics (clinical)DNA Primers030304 developmental biologyGenetics0303 health sciencesSequence Homology Amino AcidbiologyReverse Transcriptase Polymerase Chain Reactionmusculoskeletal systemmedicine.diseaseMolecular biologyTropomyosinCongenital myopathyPedigree3. Good healthHaplotypesNeurologyMutationPediatrics Perinatology and Child Healthbiology.proteinFemaleNeurology (clinical)Sequence Alignment030217 neurology & neurosurgeryCentral core diseaseNeuromuscular Disorders
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pcaH, a molecular marker for estimating the diversity of the protocatechuate-degrading bacterial community in the soil environment

2007

Microorganisms degrading phenolic compounds play an important role in soil carbon cycling as well as in pesticide degradation. The pcaH gene encoding a key ring-cleaving enzyme of the -ketoadipate pathway was selected as a functional marker. Using a degenerate primer pair, pcaH fragments were cloned from two agricultural soils. Restriction fragment length polymorphism (RFLP) screening of 150 pcaH clones yielded 68 RFLP families. Comparison of 86 deduced amino acid sequences displayed 70% identity to known PcaH sequences. Phylogenetic analysis results in two major groups mainly related to PcaH sequences from Actinobacteria and Proteobacteria phyla. This confirms that the developed primer pai…

Genetic Markers[SDV]Life Sciences [q-bio]Molecular Sequence DataBACTERIAL COMMUNITYSequence alignmentProtocatechuate-34-DioxygenaseActinobacteriaSOIL DNAchemistry.chemical_compoundBacterial ProteinsSequence Analysis ProteinMolecular markerProteobacteriaAmino Acid SequencePesticidesPhylogenySoil MicrobiologyPROTOCATECHUATE 34-DIOXYGENASEDNA PrimersGeneticsbiologyPhylogenetic treeRESTRICTION FRAGMENT LENGTH POLYMORPHISMPOLYMORPHISME DE RESTRICTIONBiodiversityGeneral Medicinebiology.organism_classificationCarbonActinobacteriaBiodegradation EnvironmentalchemistryGenetic markerInsect Science[SDE]Environmental SciencesRFLPProteobacteriaRestriction fragment length polymorphismSequence AlignmentAgronomy and Crop ScienceSoil microbiologyPolymorphism Restriction Fragment LengthPest Management Science
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Analysis of population genetic structure and variability using RAPD markers in the endemic and endangered Limonium dufourii (Plumbaginaceae)

1998

Limonium dufourii (Plumbaginaceae) is a triploid species, with apomictic reproduction, endemic to the east mediterranean coast of Spain, where it is present in only six populations with a few individuals in most of them. L. dufourii is included in the Red List of Endangered Species by the IUCN. Genetic variation and population structure in this species has been studied using RAPDs. Twelve different primers provided 124 reliable bands of which 33 were polymorphic among the 165 individuals analysed. Those polymorphic bands were able to define 44 different patterns, of which all but six were present in only one population. Several methods for statistical evaluation have been used for intra- an…

Genetic Markerseducation.field_of_studyEcologyPopulationEndangered speciesGenetic VariationPlantsBiologyAnalysis of molecular varianceRandom Amplified Polymorphic DNA TechniqueRAPDGenetics PopulationSpainEvolutionary biologyGenetic structureGenetic variationGeneticsIUCN Red ListGenetic variabilityeducationPhylogenyEcology Evolution Behavior and SystematicsDNA PrimersMolecular Ecology
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A NEW PCR-BASED TYPING OF THE RODGERS AND CHIDO ANTIGENIC DETERMINANTS OF THE FOURTH COMPONENT OF HUMAN COMPLEMEMT

1994

The Rodgers (Rg) and Chido (Ch) blood groups are antigenic determinants of the fourth component of human complement C4. They are associated with the two isotypes of C4, C4A and C4B, respectively. They serve as markers to distinguish C4A from C4B as well as for the definition of subtypes of common and rare allotypes. As an alternative to the serological typing method using human alloantisera, a PCR typing procedure with sequence-specific primers (PCR-SSP) was designed. The method was tested on selected DNA samples from individuals with well-defined C4 allotypes. No false-positive or false-negative typing results were obtained and all the determinant combinations could be distinguished. The P…

GeneticsAntigenicityGenotypeImmunologyC4ABiologyPolymerase Chain ReactionIsotypelaw.inventionBlood Grouping and CrossmatchinglawGenotypeBlood Group AntigensComplement C4bGeneticsHumansTypingAlleleGenotypingAllelesPolymerase chain reactionDNA PrimersEuropean Journal of Immunogenetics
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Screening and identification ofvipgenes inBacillus thuringiensisstrains

2009

Aims:  To identify known vip genes and to detect potentially novel vip genes in a collection of 507 strains of Bacillus thuringiensis. Methods and Results:  Following a polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) strategy, four restriction patterns were found within the vip1 family: vip1Aa1, vip1Ba1/vip1Ba2 and vip1Ca. In the screening of vip2 genes, patterns similar to those of vip2Aa1, vip2Ba1/vip2Ba2 and vip2Ac1 genes were observed. Patterns for vip3Aa1, vip3Ae2 and vip3Af1 were found among vip3 genes. Two new patterns revealed novel vip1 and vip3A genes. The observed frequency of genes belonging to vip1 and vip2 families was around 10%, whereas 48·9% of…

GeneticsBacillaceaeVasoactive intestinal peptideBacillus thuringiensisSequence Analysis DNAGeneral MedicineBiologybiology.organism_classificationPolymerase Chain ReactionApplied Microbiology and BiotechnologyGenetic analysisMolecular biologylaw.inventionBacterial ProteinsGene FrequencylawBacillus thuringiensisGene expressionRestriction fragment length polymorphismGenehormones hormone substitutes and hormone antagonistsPolymerase chain reactionDNA PrimersBiotechnologyJournal of Applied Microbiology
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Screening for multiple hereditary hypercoagulability factors using the amplification refractory mutation system

2003

Many hereditary factors have been implicated in the development of arterial and/or venous thromboembolic diseases. A number of these risk factors can be identified by the amplification refractory mutation system (ARMS). However, the underlying technical conditions for performing ARMS are highly variable, and depend on which risk factors are being analyzed. We have now developed a novel ARMS-based system to simultaneously screen for multiple hypercoagulability factors under identical PCR conditions. This can greatly simplify the process of screening for hereditary hypercoagulability.

GeneticsBase SequenceGenetic Carrier ScreeningHomozygoteGenetic Carrier ScreeningSingle-strand conformation polymorphismBlood ProteinsHematologyBlood Coagulation DisordersBiologymedicine.diseaseThrombophiliaBioinformaticsPolymerase Chain ReactionThrombosisBlood Coagulation FactorsRefractoryMutation (genetic algorithm)medicineCoagulopathyHumansMass ScreeningRisk factorDNA PrimersThrombosis Research
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Report of the European DNA profiling group (EDNAP): an investigation of the complex STR loci D21S11 and HUMFIBRA (FGA).

1997

This paper describes a collaborative exercise which was intended to demonstrate whether uniformity of DNA profiling results could be achieved between European laboratories using two complex short tandem repeat (STR) loci. The loci D21S11 and HUMFIBRA (FGA) were chosen because they are commonly used by different European laboratories. D21S11 has approximately 14 common alleles (f > 0.001), whereas HUMFIBRA has 19 common alleles. Laboratories were asked to test seven blood stains, one of which was a known control, and to report the results to the coordinating laboratory. The exercise demonstrated that complex STRs were amenable to standardisation.

GeneticsBlood StainsRepetitive SequencesReproducibility of ResultsDNABiologyPathology and Forensic MedicineEuropeDNA profilingMulticenter studyGenetic markerStr lociMicrosatelliteHumansLaboratoriesLawAllelesDNA PrimersRepetitive Sequences Nucleic AcidForensic science international
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