Search results for "length polymorphism"

showing 10 items of 177 documents

Molecular characterisation of the species of the genus Zygosaccharomyces.

2003

The restriction fragments polymorphisms of the mitochondrial DNA and the PCR fragment that comprised the internal transcribes spacers and the 5.8S rRNA gene, together with the electrophoretic karyotypes of 40 strains from the 10 species of the genus Zygosaccharomyces, including the new species Z. lentus were examined. The RFLP's of the ITS-5.8S region showed a specific restriction pattern for each species, including the new species Z. lentus. The only exception were the species Z. cidri and Z. fermentati that produced identical restriction profiles. The electrophoretic chromosome patterns confirmed the differences between the species of this genus, including the phylogenetic closest species…

GeneticsPhylogenetic treebiologyZygosaccharomycesChromosomeKaryotypeGenes rRNAZygosaccharomycesbiology.organism_classificationApplied Microbiology and BiotechnologyMicrobiologyDNA MitochondrialPolymerase Chain ReactionRestriction fragmentRNA Ribosomal 5.8SGenusKaryotypingMolecular phylogeneticsDNA Ribosomal Spacerbiology.proteinRestriction fragment length polymorphismChromosomes FungalDNA FungalEcology Evolution Behavior and SystematicsPolymorphism Restriction Fragment LengthSystematic and applied microbiology
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Characterization of polymorphisms in the toxin A and B genes of Clostridium difficile.

2006

We have used six independent polymerase chain reactions (A1–A3 and B1–B3) for amplification of the entire sequence of the two toxin genes tcdA and tcdB of several Clostridium difficile strains. With this approach we have detected (1) restriction site polymorphisms which are distributed all over the genes, and (2) deletions that could be found only in tcdA. Characteristic differences between strains were mainly focused to the 5′ third of tcdB (B1 fragment) and/or the 3′ third of tcdA (A3 fragment). The possible use of our approach for typing of C. difficile toxin genes is discussed.

GeneticsPolymorphism GeneticClostridioides difficileBacterial ToxinsClostridium difficile toxin AClostridium difficile toxin BBiologyClostridium difficileMicrobiologyMolecular biologyPolymerase Chain Reactionlaw.inventionRestriction siteEnterotoxinsBacterial ProteinslawGenes BacterialGenotypeGeneticsTypingRestriction fragment length polymorphismMolecular BiologyPolymerase chain reactionPolymorphism Restriction Fragment LengthFEMS microbiology letters
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GENETIC POLYMORPHISM OF THE FOURTH COMPONENT OF HUMAN COMPLEMENT: POPULATION STUDY AND PROPOSAL FOR A REVISED NOMENCLATURE BASED ON GENOMIC PCR TYPIN…

1996

SUMMARY The fourth component of human complement (C4) is coded for by two homologous genes, C4A and C4B, located in the class III region of the major histocompatibility complex (MHC). Genetic typing of C4A and B alleles is routinely carried out by high-voltage agarose gel electrophoresis. The electrophoretic C4 polymorphism can be further subdivided by the Rodgers (Rg) and Chido (Ch) blood groups, which are antigenic determinants of the C4A and B alpha-chains, respectively. We have used a recently described direct PCR typing method using sequence-specific primers (PCR-SSP) in combination with electrophoretic C4 typing as well as genomic RFLP analysis to determine the frequency of C4 allotyp…

GeneticsPolymorphism GeneticPopulationImmunologyHaplotypeComplement C4General MedicineBiologyPolymerase Chain ReactionAllotypeTransplantationEpitopesPolymorphism (computer science)GeneticsHumansTypingRestriction fragment length polymorphismAlleleMolecular BiologyGenotypingGenetics (clinical)International Journal of Immunogenetics
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A report of an international collaborative experiment to demonstrate the uniformity obtainable using DNA profiling techniques

1992

This paper describes a collaborative exercise intended to demonstrate whether uniformity of DNA profile results could be achieved between different European laboratories. It was shown that this goal can be obtained provided that a common protocol is followed (specifically the use of a common electrophoretic buffer as being the most important parameter). Generally, lower molecular weight loci (with lower molecular weight fragments) such as YNH24 perform better than higher molecular weight loci such as MS43a. The results of the exercise are discussed in relation to the objectives of the European DNA profiling group (EDNAP).

GeneticsProtocol (science)Quality ControlElectrophoresis Agar GelDNA/bloodRestriction MappingComputational biologyDNABiologySettore MED/43 - MEDICINA LEGALEDNA FingerprintingPathology and Forensic MedicineDNA profilingMulticenter studyAutoradiographyHumansRestriction fragment length polymorphismLaboratoriesLawDNA Fingerprinting/standards
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Polymorphism and chromosomal localization of the porcine signal transducer and activator of transcription 5B gene (STAT5B).

2006

Signal transducers and activators of transcription (STATs) are a family of transcription factors. STAT5A and 5B are two highly related proteins encoded by two distinct genes. Transgenic knockout mice studies have indicated the importance of STAT5 proteins for the regulation of both lactation and growth performance. Moreover, different studies determine the role of STAT5 proteins in the modulation of adipocyte function. In this study, we sequenced one fragment of STAT5B gene from animals of six breeds (Duroc, Iberian, Landrace, Large White, Pie´train and Meishan) to identify genetic variants. A G/A single nucleotide polymorphism in intron 14 creates a polymorphic PstI restriction site and wa…

GeneticsRadiation Hybrid MappingPolymorphism Geneticpolymorphism porcine STAT5BSwineIntronSingle-nucleotide polymorphismGeneral MedicineQuantitative trait locusBiologyMolecular biologyChromosomes MammalianSTAT5ARestriction siteSettore AGR/17 - Zootecnica Generale E Miglioramento GeneticoFood AnimalsSTAT5 Transcription FactorAnimalsAnimal Science and ZoologyRestriction fragment length polymorphismAlleleGeneJournal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie
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Use of PCR and RFLP in fungal systematics

2020

143 ref.; International audience

GeneticsSystematics[SDV] Life Sciences [q-bio][SDV]Life Sciences [q-bio]BiologyRestriction fragment length polymorphism
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Development and characterization of 11 microsatellite markers in the rock sparrow, Petronia petronia

2006

Eleven polymorphic microsatellite loci were isolated in the passeriform Petronia petronia using the enrichment protocol FIASCO (fast isolation by AFLP of sequences containing repeats). We detected three to 13 alleles per locus in 25 specimens collected from an Italian population. The level of expected heterozygosity ranged from 0.439 to 0.856. One locus is sex linked to the Z chromosome. The total exclusionary probabilities using these loci for the first and the second parent were 0.978 and 0.999, respectively. These are the first microsatellite loci characterized from the rock sparrow that can be used for estimating population structure and for large-scale parentage analysis.

GeneticsZ chromosomeEcologybiologyLocus (genetics)biology.organism_classificationBiochemistryGeneral Biochemistry Genetics and Molecular BiologyLoss of heterozygosityRock sparrowPetroniaMicrosatelliteAmplified fragment length polymorphismSex linkageMolecular Ecology Notes
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Identification of yeasts by RFLP analysis of the 5.8S rRNA gene and the two ribosomal internal transcribed spacers

1999

The identification and classification of yeasts have traditionally been based on morphological, physiological and biochemical traits. Various kits have been developed as rapid systems for yeast identification, but mostly for clinical diagnosis. In recent years, different molecular biology techniques have been developed for yeast identification, but there is no available database to identify a large number of species. In the present study, the restriction patterns generated from the region spanning the internal transcribed spacers (ITS1 and ITS2) and the 5.8S rRNA gene were used to identify a total of 132 yeast species belonging to 25 different genera, including teleomorphic and anamorphic a…

GeneticsbiologyGenes FungalGeneral MedicineSpacer DNARibosomal RNARhodotorulabiology.organism_classificationPolymerase Chain ReactionMicrobiologySaccharomycesYeastRNA Ribosomal 5.8SYeastsIdentification (biology)Internal transcribed spacerRestriction fragment length polymorphismPolymorphism Restriction Fragment LengthEcology Evolution Behavior and Systematics
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Exploring diversity among Spanish strains of Erwinia amylovora and possible infection sources

2007

Aims:  We have examined the intraspecific diversity of a collection of 63 Spanish strains of Erwinia amylovora, isolated from 1995 to 2001, to determine whether or not they could be grouped based on phenotypic or genotypic criteria and to investigate the sources of inoculum for fire blight dissemination in Spain. Methods and Results:  Several biochemical and molecular techniques, such as miniaturized API 20E, API 50CH, ATB G-5 and API-ZYM tests, BIOLOG metabolic fingerprinting, PCR ribotyping, pulsed-field gel electrophoresis (PFGE), minisatellite-primed PCR (MSP-PCR), random amplified polymorphic DNA (RAPD) analyses and AFLP were used. We report the first identification in Spain of the PFG…

Geneticsbiologyfood and beveragesOutbreakGeneral MedicineErwiniabacterial infections and mycosesbiology.organism_classificationApplied Microbiology and Biotechnologylaw.inventionRAPDlawparasitic diseasesGenotypeFire blightPulsed-field gel electrophoresisAmplified fragment length polymorphismPolymerase chain reactionBiotechnologyJournal of Applied Microbiology
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A genetic linkage map ofPhysocarpus, a member of the Spiraeoideae (Rosaceae), based on RAPD, AFLP, RGA, SSR and gene specific markers

2008

Physocarpus opulifolius is a deciduous shrub native to North America belonging to the Spiraeoideae subfamily of the Rosaceae. The cultivars 'Luteus' and 'Diabolo' are grown in gardens for their ornamental foliage, golden and purple respectively. We developed a linkage map of P. opulifolius with a view to detecting markers for the leaf colour genes, which are under major gene control. A total of 162 molecular markers (128 RAPDs, 27 AFLPs, three RGA, three STS markers and one SSR) and the leaf colour genes Pur and Aur were scored in the Physocarpus progeny and used to create a linkage map covering 586.1 cM over nine linkage groups. There was an average of 18.2 markers per linkage group and a …

Geneticsbiologyfood and beveragesPlant Sciencebiology.organism_classificationRAPDSettore AGR/03 - Arboricoltura Generale E Coltivazioni Arboreechemistry.chemical_compoundPhysocarpus opulifoliusSpiraeoideaechemistryGene mappingGenetic linkageSettore AGR/07 - Genetica AgrariaMolecular markerGeneticsPhysocarpusAmplified fragment length polymorphismAgronomy and Crop Sciencecomparative mapping — Spireaeoideae — Rosaceae — molecular markerPlant Breeding
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