Search results for "Genomic DNA"

showing 10 items of 67 documents

A simple sequence repeat-based linkage map of barley.

2000

Abstract A total of 568 new simple sequence repeat (SSR)-based markers for barley have been developed from a combination of database sequences and small insert genomic libraries enriched for a range of short simple sequence repeats. Analysis of the SSRs on 16 barley cultivars revealed variable levels of informativeness but no obvious correlation was found with SSR repeat length, motif type, or map position. Of the 568 SSRs developed, 242 were genetically mapped, 216 with 37 previously published SSRs in a single doubled-haploid population derived from the F1 of an interspecific cross between the cultivar Lina and Hordeum spontaneum Canada Park and 26 SSRs in two other mapping populations. A …

GeneticsGenetic Markerseducation.field_of_studyDNA PlantGenetic LinkagePopulationfood and beveragesChromosome MappingHordeumBiologyGenes Plantgenomic DNAGene mappingGenetic markerGenetic linkageGeneticsMicrosatelliteGenomic libraryRestriction fragment length polymorphismeducationCrosses GeneticGenome PlantResearch ArticleRepetitive Sequences Nucleic Acid
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Development of “universal” gene-specific markers from Malus spp. cDNA sequences, their mapping and use in synteny studies within Rosaceae

2009

The Rosaceae contains many economically valuable crop genera, including Malus (apple), Fragaria (strawberry), and Prunus (stone fruit). There has been increasing interest in the development of linkage maps for these species, with a view to marker-assisted selection to assist breeding programs and, recently, in the development of transferable markers to permit syntenic comparisons of maps of different rosaceous genera. In this investigation, a set of Malus cDNA sequences were downloaded from the European Molecular Biology Laboratory database. The sequences were aligned with homologous full-length Arabidopsis genomic DNA sequences to identify putative intron–exon junctions and conserved flank…

GeneticsMaluseducation.field_of_studybiologyPopulationForestryGenomicsHorticulturebiology.organism_classificationGenomegenomic DNAGene mappingComplementary DNASettore AGR/07 - Genetica AgrariaGeneticseducationMolecular BiologyArabidopsis Comparative mapping Rosaceae Bin mapping Fragaria PrunusSynteny
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Molecular cloning ofTrichophyton mentagrophytes DNA sequences with promoter activity inEscherichia coli

1992

A promoter probe library from the dermatophyte fungusTrichophyton mentagrophytes has been constructed in the pVB32 plasmid vector. Using this library, a set ofT. mentagrophytes DNA sequences with promoter activity inEscherichia coli has been cloned. The size and the resistance phenotype conferred by these DNA fragments varied. Southern blot analysis confirmed that they were derived fromT. mentagrophytes genomic DNA.

GeneticsPhysiologyNucleic acid sequenceGeneral MedicineMolecular cloningBiologymedicine.disease_causeApplied Microbiology and BiotechnologyMolecular biologyDNA sequencinggenomic DNAchemistry.chemical_compoundPlasmidchemistrymedicineEscherichia coliDNABiotechnologySouthern blotWorld Journal of Microbiology and Biotechnology
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Paternity Analysis Using the Multilocus DNA Probe MZ 1.3

1992

The multilocus minisatellite DNA probe MZ 1.3 detects hypervariable restriction fragment patterns in genomic DNA of man and animals. It can be used for segregation analysis in cases of disputed paternity (Schacker et al., 1991; Rittner et al., 1991a), for identification purposes in forensic medicine and stain analysis (Ogata et al., 1990; Rittner et al., 1991b), as well as in animal breeding for pedigree analysis and verification of inbred strains (Hins & Gruber, 1991). Hypervariable fragment patterns can be generated by using frequently cutting restriction enzymes, e.g. Hinf I, Hae Ill, Msp I, Mbo I, and Rsa I. A non-radioactive system using the digoxigenin antidigoxigenin system may be us…

GeneticsRestriction enzymechemistry.chemical_compoundgenomic DNAMinisatellitechemistryInbred strainHybridization probebiology.proteinDigoxigeninBiologyDNARestriction fragment
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Application of whole genome amplification for forensic analysis

2006

Abstract Fundamental to most forensic analyses is the availability of genomic DNA of adequate quality and quantity. To perform a multitude of genetic analyses and assays requires a sufficiently large amount of template. However, DNA yield from forensic samples is frequently limiting the extent of genetic typing. A possible solution to overcome this “bottleneck” of forensic and paleoarcheological DNA analyses could be the amplification of the entire genomic DNA prior to locus specific PCR analysis. Whole Genome Amplification appears to be a promising tool to obtain sufficient DNA amounts from forensic samples of limited quantity.

GeneticsWhole Genome AmplificationForensic sciencechemistry.chemical_compoundgenomic DNAchemistryDna concentrationMultiple displacement amplificationLocus (genetics)General MedicineBiologyPcr analysisDNA
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Cloning and characterization of the histidine biosynthetic gene cluster of Streptomyces coelicolor A3(2).

1990

Abstract Biochemical and genetic data indicate that in Streptomyces coelicolor A3(2) the majority of the genes involved in the biosynthesis of histidine are clustered in a small region of the chromosome [Carere et al., Mol. Gen. Genet. 123 (1973) 219–224; Russi et al., Mol. Gen. Genet. 123 (1973) 225–232]. To investigate the structural organization and the regulation of these genes, we have constructed genomic libraries from S. coelicolor A3(2) in pUC vectors. Recombinant clones were isolated by complementation of an Escherichia coli hisBd auxotroph. A recombinant plasmid containing a 3.4-kb fragment of genomic DNA was further characterized. When cloned in the plasmid vector, pIJ699, this f…

GeneticsbiologyBase SequenceOperonStreptomyces coelicolorGenes FungalGenetic Complementation TestMolecular Sequence DataRestriction MappingNucleic acid sequencehisBGeneral MedicineMolecular cloningbiology.organism_classificationMolecular biologyStreptomycesgenomic DNAGene clusterGeneticsEscherichia coliGenomic libraryHistidineAmino Acid SequenceCloning MolecularPlasmidsGene
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Phylogenetic relationships between Drosophila subobscura, D. guanche and D. madeirensis based on Southern analysis of heat shock genes.

2004

A Southern analysis of genomic DNA using Drosophila melanogaster probes for the major heat shock protein genes (Hsp82, Hsp 70, Hsps encoding small proteins) was made to study the phylogenetic relationships between three Drosophila species belonging to the obscura group (D. subobscura, D. guanche, and D. madeirensis). The phylogenetic trees showed that D. madeirensis and D. subobscura are the most closely related species in the triad, while D. guanche is the most distantly related one. As in other Drosophila species, Hsp82 is a single copy gene in D. subobscura, D. guanche, and D. madeirensis, while Hsp 70 and Hsps, which encode small proteins, are genie families. At least four sequences hom…

GeneticsbiologyPhylogenetic treeRestriction MappingGenetic VariationGeneral Medicinebiology.organism_classificationDrosophila subobscuragenomic DNABlotting SouthernDrosophila melanogasterHeat shock proteinGeneticsMelanogasterAnimalsDrosophilaDrosophila (subgenus)Drosophila melanogasterGeneHeat-Shock ProteinsPhylogenyHereditas
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Fingerprinting ofCaprinae ancient genomic DNA: A preliminary note for studying the history of domestication in sicily

1996

Oligonucleotide primers representing promoter and protein motifs in rats and mice were assayed for PCR amplification of ancient DNA from two sheep and one goat. We show preliminary evidence that this type of primers can be used for genomic fingerprinting of ancient DNA at interspecific level and can help in solving some paleoecological promlems.

Geneticsbiologyfungifood and beveragesbiology.organism_classificationlaw.inventionCaprinaechemistry.chemical_compoundgenomic DNAAncient DNADNA profilingchemistrylawAnthropologyCapraDomesticationPolymerase chain reactionDNAHuman Evolution
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Polymorphisms in the intergenic region of the sea urchin Paracentrotus lividus ribosomal DNA

1990

Abstract Blot-hybridizations of the sea urchin Paracentrotus lividus genomic DNA with ribosomal DNA (rDNA) probes revealed individual variations in the length and in the sequence of the non-transcribed spacer (NTS) region. The number of rDNA repeat subclasses distinguishable within any individual sea urchin is usually limited (1 to 3) with respect to the widest polymorphism of the population as a whole. The heterogeneity in sequence is revealed by the presence or the absence of specific restriction sites in the spacer region. The data obtained by the intensity of the polymorphic bands indicate that different mechanisms bring about these two types of polymorphism. Preliminary data also indic…

Geneticseducation.field_of_studybiologyPopulationCell Biologybiology.organism_classificationParacentrotus lividusgenomic DNARestriction siteRestriction mapIntergenic regionbiology.animaleducationRibosomal DNASea urchinCell Biology International Reports
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Beta-lactoglobulin polymorphism in Girgentana goat breed

2007

Beta-lactoglobulin (b-lg) is a globular protein belonging to the lipocalin family. It is the major whey protein in the milk of ruminants. It is also present in the milk of most mammals but is lacking in rodents, lagomorphs and humans. A large number of variants have been reported for cow and sheep milk. Several studies have shown association between b-lg variants and milk production and composition, even if the results are not always concordant. In goat, no b-lg variants related with amino acid change have been characterized at DNA level, but some authors described the presence of polymorphisms in the 3’UTR and in the proximal promoter region. Mutations in the promoter region could be those…

Geneticsfood and beveragesPromoterBiologyBreedgenomic DNAchemistry.chemical_compoundSettore AGR/17 - Zootecnica Generale E Miglioramento GeneticochemistryGene expressionbiology.proteinBeta-lactoglobulin polymorphisms Girgentana goat breedAnimal Science and Zoologylcsh:Animal cultureSheep milkGeneBeta-lactoglobulinDNAlcsh:SF1-1100
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