Search results for " Mapping"

showing 10 items of 1411 documents

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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Distribution of gypsy sequences in Drosophila species of the obscura subgroup.

2004

Eight Drosophila species of the obscura subgroup were screened for sequences homologous to the gypsy retrotransposon of D. melanogaster. Molecular characterization of gypsy sequences was first approached through digesting genomic DNAs from these obscura species with appropriate restriction enzymes and subjecting them to Southern blot analysis. The results of this analysis indicate that gypsy-homologous sequences are well conserved among species of the obscura subgroup. With the exception of D. guanche, all other species bear a 7 kb Xho I fragment that represents the complete element in D. melanogaster. Lower molecular weight fragments that could be deleted elements, are shared by different …

GeneticsbiologyRestriction MappingNucleic Acid HybridizationRetrotransposonGeneral MedicineDNAbiology.organism_classificationRestriction enzymeBlotting SouthernSpecies SpecificityMolecular evolutionDrosophilidaeGeneticsMelanogasterDNA Transposable ElementsAnimalsDrosophilaDrosophila (subgenus)Southern blotGenomic organizationHereditas
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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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Assignment of enolase processed pseudogene (ENO1P) to human chromosome 1 bands 1q41→q42

1996

Geneticschemistry.chemical_classificationPhosphopyruvate hydratasePseudogeneEnolaseChromosome MappingChromosomeBiologyEnzymeGene mappingchemistryBiochemistryChromosomes Human Pair 1Phosphopyruvate HydrataseGeneticsHumansMolecular BiologyGeneIn Situ Hybridization FluorescencePseudogenesGenetics (clinical)Carbon-Oxygen LyasesCytogenetic and Genome Research
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Genetic differentiation in the striped dolphin Stenella coeruleoalba from European waters according to mitochondrial DNA (mtDNA) restriction analysis

1999

We used mitochondrial DNA (mtDNA) restriction analysis to study genetic variation in 98 striped dolphins (Stenella coeruleoalba) stranded on coasts from different European countries and from animals caught by fisheries. A total of 63 different restriction sites was mapped after digestion of mtDNA with 15 restriction endonucleases that yielded a total of 27 haplotypes. No haplotype was shared between Mediterranean and Atlantic areas. All the analyses indicate the existence of two different populations with a very limited gene flow across the Strait of Gibraltar.

Geneticseducation.field_of_studyMitochondrial DNADolphinsRestriction MappingPopulationGenetic VariationZoologyStenella coeruleoalbaBiologyDNA MitochondrialEuropeRestriction Site PolymorphismRestriction siteRestriction enzymeGenetics PopulationRestriction mapHaplotypesbiology.animalGenetic variationGeneticsAnimalseducationPhylogenyEcology Evolution Behavior and SystematicsMolecular Ecology
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Exploring Evolution in Ceboidea (Platyrrhini, Primates) by Williams-Beuren Probe (HSA 7q11.23) Chromosome Mapping

2007

The ancestral platyrrhine karyotype was characterised by a syntenic association of human 5 and a small segment of human 7 orthologues. This large syntenic association has undergone numerous rearrangements in various phylogenetic lines. We used a locus-specific molecular cytogenetic approach to study the chromosomal evolution of the human 7q11.23 orthologous sequences (William-Beuren syndrome, WS) in various Ceboidea (Platyrrhini) species. The fluorescent in situ hybridisation of the WS probe revealed a two-way pattern of chromosomal organisation that suggests various evolutionary scenarios. The first pattern (seen in Callimico and Saimiri ) includes a fairly simple disruption of the 7/5 syn…

Geneticsmedicine.diagnostic_testPhylogenetic treeChromosome MappingChromosomeKaryotypePlatyrrhiniSettore BIO/08 - AntropologiaBiologybiology.organism_classificationBiological EvolutionAtelinaeMOLECULAR CYTOGENETICS PRIMATES EVOLUTION WILLIAMS SYNDROME LOCUS NEOTROPICAL MONKEYS SYNTENY 7 FLUORESCENCE IN SITU HYBRIDISATION PHYLOGENYPhylogeneticsCebidaemedicineAnimalsAnimal Science and ZoologyEcology Evolution Behavior and SystematicsFluorescence in situ hybridizationSyntenyFolia Primatologica
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PATTERNS OF PUFFING ACTIVITY AND CHROMOSOMAL POLYMORPHISM IN DROSOPHILA SUBOBSCURA . IV. EFFECT OF INVERSIONS ON GENE EXPRESSION

1988

We have observed that, contrary to a common assumption, the puffing patterns manifest in the salivary chromosomes of Drosophila subobscura are modified by chromosomal inversions as well as by genic content. An inversion effect is apparent in the E and A chromosomes of five strains coming from four different natural populations. An effect due to the geographical location of the populations is also detected in the J and O chromosomes. The chromosomal and geographic effects are distinguishable but not contradictory. Indeed, a statistical test using the DK2 coefficient of distance shows that, for a given chromosomal arrangement, strains of different geographic origin exhibit puffing patterns si…

Geneticsmedicine.medical_specialtyPolytene chromosomeCytogeneticsChromosomeBiologybiology.organism_classificationDrosophila subobscuraGene mappingDrosophilidaeGeneticsmedicineChromosomal polymorphismGeneral Agricultural and Biological SciencesEcology Evolution Behavior and SystematicsChromosomal inversionEvolution
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Differences in gene activity in a Drosophila species cluster belonging to the Obscura group

1993

The polytene chromosome puffing pattern of Drosophila madeirensis was established and compared with those of the related species D. subobscura and D. guanche. A total of 145 loci, active in some of the 12 developmental stages analysed, were described, 38 of which were found to form the puffing pattern characteristic to this species. Taking into account the number of puffs as well as the mean puff expression, D. madeirensis shows a similar activity level to D. guanche, both species being less active than D. subobscura. The low gene activity of D. madeirensis and D. guanche was explained as a consequence of their ecological characteristics.

Geneticsmedicine.medical_specialtyPolytene chromosomePortugalbiologyPolytene chromosome puffingCytogeneticsGene Expressionbiology.organism_classificationChromosomesDrosophila subobscuraGene mappingEvolutionary biologyLarvaDrosophilidaeGeneticsmedicineAnimalsDrosophilaFemaleGene activityDrosophila (subgenus)PhylogenyGenetics (clinical)Heredity
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Nucleotide sequence of plasmid p4028, a cryptic plasmid from Leuconostoc oenos.

1996

Abstract TheLeuconostoc oenosplasmid p4028 was cloned in pBlueScript (SK+), and its complete nucleotide sequence was determined. The analysis of the nucleotide sequence revealed five open reading frames, all of them located on the same strand and grouped in two clusters separated by a short noncoding stretch. A similarity search against the other sequences deposited in the EMBL and GenBank databases showed that p4028 has no significant similarity with any of the sequences checked. Nevertheless, a putative ATP-binding motif was found in ORF2. A more detailed analysis of this ORF suggests that it could encode for a DNA-dependent ATPase.

GeneticspBluescriptbiologyBase SequenceATPaseGenetic VectorsMolecular Sequence DataRestriction MappingNucleic acid sequenceMolecular biologyOpen reading frameOpen Reading FramesPlasmidCryptic plasmidBacterial ProteinsGenBankbiology.proteinAmino Acid SequenceCloning MolecularMolecular BiologyLeuconostocPlasmidsPlasmid
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Genomic structure and paralogous regions of the inversion breakpoint occurring between human chromosome 3p12.3 and orangutan chromosome 2.

2003

Intrachromosomal duplications play a significant role in human genome pathology and evolution. To better understand the molecular basis of evolutionary chromosome rearrangements, we performed molecular cytogenetic and sequence analyses of the breakpoint region that distinguishes human chromosome 3p12.3 and orangutan chromosome 2. FISH with region-specific BAC clones demonstrated that the breakpoint-flanking sequences are duplicated intrachromosomally on orangutan 2 and human 3q21 as well as at many pericentromeric and subtelomeric sites throughout the genomes. Breakage and rearrangement of the human 3p12.3-homologous region in the orangutan lineage were associated with a partial loss of dup…

Genome evolutionHerpesvirus 4 HumanPan troglodytesBiologyHybrid CellsChimpanzee genome projectEvolution MolecularContig MappingChromosome 19Pongo pygmaeusGeneticsAnimalsHumansLymphocytesMolecular BiologyGenetics (clinical)In Situ Hybridization FluorescenceChromosomal inversionCell Line TransformedSequence DeletionGeneticsHuman evolutionary geneticsCercopithecidaeChromosome BreakageGenome projectChromosomes MammalianChromosome InversionChromosomes Human Pair 3Chromosome breakageChromosome 21Cytogenetic and genome research
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