Search results for " nucleic acid"

showing 10 items of 272 documents

Subrepeats result from regional DNA sequence conservation in tandem repeats in Chironomus telomeres

1990

Repeat units, widespread in eukaryotic genomes, are often partially or entirely built up of subrepeats. Homogenization between whole repeat units arranged in tandem usually can best be understood as a result of unequal crossing over. Such a mechanism is less plausible for maintaining similarities between subrepeats within a repeat unit when present in a regular array. In Chironomus telomeres, large blocks of tandemly repeated approximately 350 base-pair units contain two or three pairs of subrepeats with high mutual identities, embedded in linker DNA, non-repetitive within the repeat unit. Measurements of evolutionary base changes in two closely related species, Chironomus tentans and Chiro…

GeneticsGenomic LibraryUnequal crossing overBase SequencebiologyMolecular Sequence DataGene AmplificationDNAbiology.organism_classificationBiological EvolutionGenomeLinker DNAChironomidaeDNA sequencingSpecies SpecificityTandem repeatStructural BiologyMolecular evolutionSequence Homology Nucleic AcidAnimalsChironomusMolecular BiologyRepetitive Sequences Nucleic AcidRepeat unitJournal of Molecular Biology
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Considerations from the European DNA profiling group (EDNAP) concerning STR nomenclature

1997

(1) The nomenclature of any STR follows from comparison with a control allelic ladder; availability of reference allelic ladders is central to any scheme. The components of an allelic ladder should be sequenced. (2) The DNA commission recommended a nomenclature based upon the number of repeat sequences present in an allele. Whereas this method is suitable for typing simple STRs, complex hypervariable repeats such as ACTBP2 do not conform to a simple repeating structure. We propose that designation of complex STR repeats such as ACTBP2, D11S554 and APOAI1 follows from the size of specific alleles. Because the size is dependant upon the primers utilised, the size is not definitive (it may als…

GeneticsLocus (genetics)DNASequence Analysis DNAForensic MedicineBiologyActinsPathology and Forensic MedicineEuropeType (biology)DNA profilingGenetic markerPolymorphism (computer science)Terminology as TopicHumansMicrosatelliteTypingAlleleLawSocieties MedicalRepetitive Sequences Nucleic AcidForensic Science International
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Forensics of birds of prey by DNA fingerprinting with 32P-labeled oligonucleotide probes.

1991

Paternity tests on confiscated families of eight species of birds of prey were carried out successfully by DNA fingerprinting with 32P-labeled oligonucleotide probes. Variations in the number of hybridized fragments, depending on the species of birds, are observed using the same probe, as well as differences of polymorphism by hybridizing the DNA samples with several oligonucleotide probes.

GeneticsMaleBase CompositionBase SequenceOligonucleotideClinical BiochemistryPhosphorus IsotopesBiologyBiochemistryDNA FingerprintingAnalytical ChemistryPredationBirdschemistry.chemical_compoundchemistryDNA profilingPolymorphism (computer science)Paternity testsAnimalsBase sequenceMolecular probeOligonucleotide ProbesDNAPolymorphism Restriction Fragment LengthRepetitive Sequences Nucleic AcidElectrophoresis
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Basic issues in forensic DNA typing

1997

DNA analysis has become the standard method in forensic stain typing (termed DNA profiling). In contrast to conventional serological methods, any human tissue or body fluid can be analysed by DNA profiling as long as it contains nucleated cells. The majority of genetic systems studied at the DNA level are derived from "non-coding" portions from the human genome, and are located either in the vicinity of expressed (coding) genes or in stretches of DNA sequences interspersing with the genes. The typing results are usually recorded as DNA fragment lengths or "alleles" indicating the number of core repeat elements for short tandem repeat systems. These typing results do not contain any useful i…

GeneticsPolymorphism GeneticGenotypeGenome HumanDNAForensic MedicineBiologyDNA FingerprintingGenomeDNA sequencingPathology and Forensic MedicinePhenotypeDNA profilingGenetic markerHumansMultilocus sequence typingMicrosatelliteHuman genomeTypingLawAllelesRepetitive Sequences Nucleic AcidForensic Science International
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Intragenomic recombination between homologous regions of genes II and IV promotes formation of bacteriophage f1 miniphages.

1987

GeneticsRecombination GeneticBase SequenceGenes ViralDNA Restriction EnzymesBiologybiology.organism_classificationColiphagesVirusHomology (biology)BacteriophageSequence Homology Nucleic AcidGeneticsHomologous chromosomeBase sequenceDeoxyribonucleases Type II Site-SpecificGeneRecombinationNucleic acids research
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New Foldback transposable element TFB1 found in histone genes of the midge Chironomus thummi

1990

A new Foldback transposable element (TFB1) has been found in the histone H1-H3 intergenic region in the midge Chironomus thummi thummi. TFB1 has long terminal inverted repeats, composed of short, degenerate subrepeats and is flanked by nine or ten base-pair “target site” duplications. TFB1 is present in at least two adjacent histone gene units in Ch. th. thummi, indicating a homogenization of histone gene repeats. The copy number and chromosomal distribution of TFB1 are different in the closely related subspecies Ch. th. thummi and Ch. th. piger, showing that amplification, elimination and transposition of TFB1 have occurred recently during evolution.

GeneticsTransposable elementBase SequenceFoldback (sound engineering)Inverted repeatMolecular Sequence DataRestriction MappingGene AmplificationNucleic acid sequenceBiologyBiological EvolutionChironomidaeHistonesTransposition (music)Intergenic regionHistoneStructural BiologyMutationDNA Transposable Elementsbiology.proteinAnimalsMolecular BiologyGeneRepetitive Sequences Nucleic AcidJournal of Molecular Biology
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Sequences homologous to the hobo transposable element in E strains of Drosophila melanogaster.

2001

Hobo is one of the three Drosophila melanogaster transposable elements, together with the P and I elements, that seem to have recently invaded the genome of this species. Surveys of the presence of hobo in strains from different geographical and temporal origins have shown that recently collected strains contain complete and deleted elements with high sequence similarity (H strains), but old strains lack hobo elements (E strains). Besides the canonical hobo sequences, both H and E strains show other poorly known hobo-related sequences. In the present work, we analyze the presence, cytogenetic location, and structure of some of these sequences in E strains of D. melanogaster. By in situ hybr…

GeneticsTransposable elementbiologyEuchromatinBase SequenceChromosome MappingDNASequence Analysis DNAbiology.organism_classificationGenomeChromosomesDrosophila melanogasterSequence Homology Nucleic AcidGeneticsMelanogasterHomologous chromosomeDNA Transposable ElementsAnimalsDrosophila melanogasterMolecular BiologySequence AlignmentEcology Evolution Behavior and SystematicsTransposaseIn Situ HybridizationSequence (medicine)Molecular biology and evolution
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Arthropod 7SK RNA

2008

The 7SK small nuclear RNA (snRNA) is a key player in the regulation of polymerase (pol) II transcription. The 7SK RNA was long believed to be specific to vertebrates where it is highly conserved. Homologs in basal deuterostomes and a few lophotrochozoan species were only recently reported. On longer timescales, 7SK evolves rapidly with only few conserved sequence and structure motifs. Previous attempts to identify the Drosophila homolog thus have remained unsuccessful despite considerable efforts. Here we report on the discovery of arthropod 7SK RNAs using a novel search strategy based on pol III promoters, as well as the subsequent verification of its expression. Our results demonstrate th…

GeneticsbiologyComputational BiologyGene Expression7SK Small Nuclear RNAPrp24RNA polymerase IINon-coding RNARNA polymerase IIIConserved sequenceDrosophila melanogasterEvolutionary biologyRNA Small NuclearSequence Homology Nucleic AcidDatabases GeneticGeneticsbiology.proteinAnimalsNucleic Acid ConformationsnRNPArthropodsMolecular BiologyEcology Evolution Behavior and SystematicsSmall nuclear RNAMolecular Biology and Evolution
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Variations in Substitution Rate in Human and Mouse Genomes

2003

We present a method to quantify spatial fluctuations of the substitution rate on different length scales throughout genomes of eukaryotes. The fluctuations on large length scales are found to be predominantly a consequence of a coarse-graining effect of fluctuations on shorter length scales. This is verified for both the mouse and the human genome. We also found that both species show similar standard deviation of fluctuations even though their mean substitution rate differs by a factor of two. Our method furthermore allows to determine time-resolved substitution rate maps from which we can compute auto-correlation functions in order to quantify how fast the spatial fluctuations in substitu…

Genomics (q-bio.GN)GenomeModels GeneticGenome HumanRelative standard deviationSubstitution (logic)AutocorrelationPopulations and Evolution (q-bio.PE)Genetic VariationGeneral Physics and AstronomyGenomicsTime resolutionBiologyQuantitative Biology::GenomicsGenomeMiceEvolutionary biologyFOS: Biological sciencesAnimalsHumansQuantitative Biology - GenomicsHuman genomeQuantitative Biology - Populations and EvolutionRepetitive Sequences Nucleic Acid
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Extraction of β-blockers from urine with a polymeric monolith modified with 1-allyl-3-methylimidazolium chloride in spin column format

2020

Abstract A glycidyl methacrylate-based monolith was modified with imidazolium-based ionic liquid (IL) to be used as stationary phase for solid-phase extraction (SPE). The host monolithic support was prepared by in-situ UV polymerization in spin column format. Two approaches were developed to incorporate the IL into the polymeric monolithic matrix: generation of IL onto the surface monolith, and copolymerization by addition of the IL to the polymerization mixture, which gave the best results. The resulting sorbent materials were morphologically characterized and used for the isolation of five β-blockers from human urine samples. All SPE steps were accomplished by centrifugation, which reduce…

Glycidyl methacrylatePolymersSurface PropertiesAdrenergic beta-Antagonists02 engineering and technology01 natural sciencesHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)chemistry.chemical_compoundSpin column-based nucleic acid purificationHumansSolid phase extractionParticle SizeMonolithDetection limitgeographygeography.geographical_feature_categoryChromatographyChemistrySolid Phase Extraction010401 analytical chemistryExtraction (chemistry)Imidazoles021001 nanoscience & nanotechnology0104 chemical sciencesAllyl CompoundsEpoxy CompoundsMethacrylates0210 nano-technologyTalanta
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