Search results for "MUTATION"

showing 10 items of 2830 documents

Biostatistical basis of individualization and segregation analysis using the multilocus DNA probe MZ 1.3: results of a collaborative study.

1992

A collaborative study using the multilocus minisatellite DNA probe MZ 1.3 was carried out to investigate segregation information, mutation rate, DNA fragment frequencies as well as band sharing characteristics. The fingerprint patterns of 393 children as well as 694 unrelated individuals were analysed after digestion of DNA with the restriction enzyme HinfI. A mutation rate of 1% per meiosis or 0.04% per band was found with a mean number of 26 bands/individual. It was shown that maternal and paternal fragments are inherited in equal proportions. Population frequencies of restriction fragments demonstrated a distribution with increasing frequencies in the small fragment size range below 10 k…

GeneticsMaleMutation rateeducation.field_of_studyBiometrybiologyHybridization probePopulationPaternityDNA FingerprintingPathology and Forensic MedicineRestriction fragmentRestriction enzymeMinisatelliteDNA profilingData Interpretation Statisticalbiology.proteinHumansFemaleeducationMolecular probeChildDNA ProbesLawProbabilityForensic science international
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The STR252-IVS10nt546-VNTR7 phenylalanine hydroxylase minihaplotype in five Mediterranean samples.

1997

IVS10nt546 (IVS10nt-11g→a) is the most common molecular defect of the phenylalanine hydroxylase gene causing phenylketonuria in Mediterranean populations. Previous studies have proposed various and alternative hypotheses concerning the geographical origin and pattern of diffusion of this mutation in this area. In this study, this issue was re-examined on a large sample (149) of “Mediterranean” IVS10nt546 mutant alleles analysed with multiallelic intragenic polymorphisms. The analysis of intragenic microsatellite (STR) and minisatellite (VNTR) polymorphisms shows allelic heterogeneity of the IVS10nt546 mutation. Eight STR and three VNTR alleles were found in association with the splicing def…

GeneticsMediterranean RegionHaplotypePopulation geneticsPhenylalanine HydroxylaseMinisatellite RepeatsBiologyGene flowMinisatelliteGene FrequencyHaplotypesPhenylketonuriasMutation (genetic algorithm)GeneticsMicrosatelliteHumansPoint MutationAllelic heterogeneityAlleleGenetics (clinical)Microsatellite RepeatsHuman genetics
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Cystinuria subtype and nephrolithiasis

1999

GeneticsMembrane glycoproteinsBiochemistryNephrologyCarrier proteinMutation (genetic algorithm)biology.proteinmedicineCystinuriaBiologymedicine.diseaseKidney International
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Modern taurine cattle descended from small number of near-eastern founders.

2012

Archaeozoological and genetic data indicate that taurine cattle were first domesticated from local wild ox (aurochs) in the Near East some 10,500 years ago. However, while modern mitochondrial DNA (mtDNA) variation indicates early Holocene founding event(s), a lack of ancient DNA data from the region of origin, variation in mutation rate estimates, and limited application of appropriate inference methodologies have resulted in uncertainty on the number of animals first domesticated. A large number would be expected if cattle domestication was a technologically straightforward and unexacting region-wide phenomenon, while a smaller number would be consistent with a more complex and challengin…

GeneticsMitochondrial DNAModels Geneticved/biologySmall numberTaurine cattleved/biology.organism_classification_rank.speciesPopulation DynamicsBiologyAurochsbiology.organism_classificationDNA MitochondrialFounder EffectAncient DNAMutation RateEvolutionary biologyGeneticsAnimalsCattleFemaleApproximate Bayesian computationDomesticationMolecular BiologyEcology Evolution Behavior and SystematicsFounder effectMolecular biology and evolution
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Interactions between the yeast mitochondrial and nuclear genomes: isogenic suppressive and hypersuppressive petites differ in their resistance to the…

1990

In a previous paper we have shown that the alkaloid lycorine inhibits growth of rho+, mit- and rho-, strains of Saccharomyces cerevisiae, whereas strains devoid of mitochondrial DNA (rho degrees) are resistant to more than 200 micrograms/ml of the alkaloid. In this report we show that hypersuppressive petites are almost as resistant as rho degrees mutants, whereas isogenic rho- petites, which have retained longer segments of the genome, are sensitive to the drug.

GeneticsMitochondrial DNAMutationbiologyAlkaloidSaccharomyces cerevisiaeMutantDrug Resistance MicrobialSaccharomyces cerevisiaeGeneral Medicinebiology.organism_classificationLycorinemedicine.disease_causeDNA MitochondrialMolecular biologyGenomeYeastPhenanthridineschemistry.chemical_compoundchemistryAmaryllidaceae AlkaloidsGeneticsmedicineDNA FungalCurrent Genetics
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Results of a collaborative study of the EDNAP group regarding mitochondrial DNA heteroplasmy and segregation in hair shafts.

2004

Abstract A collaborative exercise was carried out by the European DNA Profiling Group (EDNAP) in order to evaluate the distribution of mitochondrial DNA (mtDNA) heteroplasmy amongst the hairs of an individual who displays point heteroplasmy in blood and buccal cells. A second aim of the exercise was to study reproducibility of mtDNA sequencing of hairs between laboratories using differing chemistries, further to the first mtDNA reproducibility study carried out by the EDNAP group [Forensic Sci. Int. 97 (1998) 165]. Laboratories were asked to type 2 sections from each of 10 hairs, such that each hair was typed by at least two laboratories. Ten laboratories participated in the study, and a to…

GeneticsMitochondrial DNATransition (genetics)integumentary systemBuccal swabGenetic VariationSequence Analysis DNABiologyDNA MitochondrialHeteroplasmyPathology and Forensic MedicineDNA profilingMutationHumansTypingLawHairForensic science international
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Mutated tumor alleles are expressed according to their DNA frequency

2014

AbstractThe transcription of tumor mutations from DNA into RNA has implications for biology, epigenetics and clinical practice. It is not clear if mutations are in general transcribed and, if so, at what proportion to the wild-type allele. Here, we examined the correlation between DNA mutation allele frequency and RNA mutation allele frequency. We sequenced the exome and transcriptome of tumor cell lines with large copy number variations, identified heterozygous single nucleotide mutations and absolute DNA copy number and determined the corresponding DNA and RNA mutation allele fraction. We found that 99% of the DNA mutations in expressed genes are expressed as RNA. Moreover, we found a hig…

GeneticsMultidisciplinaryDNA Copy Number VariationsPoint mutationHigh-Throughput Nucleotide SequencingRNABiologyMolecular biologyArticleMicechemistry.chemical_compoundGene FrequencychemistryTranscription (biology)Cell Line TumorNeoplasmsMutationAnimalsAlleleGeneAllele frequencyExomeAllelesDNAScientific Reports
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Prisoner's dilemma in an RNA virus

1999

The evolution of competitive interactions among viruses1 was studied in the RNA phage φ6 at high and low multiplicities of infection (that is, at high and low ratios of infecting phage to host cells). At high multiplicities, many phage infect and reproduce in the same host cell, whereas at low multiplicities the viruses reproduce mainly as clones. An unexpected result of this study1 was that phage grown at high rates of co-infection increased in fitness initially, but then evolved lowered fitness. Here we show that the fitness of the high-multiplicity phage relative to their ancestors generates a pay-off matrix conforming to the prisoner's dilemma strategy of game theory2,3. In this strateg…

GeneticsMultidisciplinarybiologyvirusesmedia_common.quotation_subjectRNARNA virusPrisoner's dilemmaVirus Replicationbiology.organism_classificationBiological EvolutionModels BiologicalVirusCystovirusBacteriophage phi 6BacteriophageGame TheoryMutationMicrobial cooperationSelfishnessmedia_commonNature
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Influence of Apo A4 genotypes (Apo4-347 mutation) on the lipid response to diet in familial hypercholesterolemia

2000

GeneticsMutation (genetic algorithm)GenotypemedicineFamilial hypercholesterolemiaBiologyCardiology and Cardiovascular Medicinemedicine.diseaseAtherosclerosis
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Adventitious bud formation on isolated leaves and its significance for mutation breeding

1968

Since a mutation is a unicellular event, irradiation of a multicellular meristem results in the so-called diplontic selection. This competition between the mutated cell and the surrounding non-mutated cells is often lost by the mutated cell, causing a low frequency of mutated plants and a narrow mutation spectrum. When a mutated cell survives, chimeras are automatically formed because most apices consist of a number of fairly independent groups of cell layers. Such an undesirable situation can be improved by growing complete plants from only one cell, resulting in a high frequency of solid, non-chimeral mutants and a wide mutation spectrum. Many plant species can be stimulated to form adven…

GeneticsMutation breedingmedia_common.quotation_subjectfungiMutantCellfood and beveragesPlant physiologyPlant ScienceHorticultureMeristemBiologyCompetition (biology)Multicellular organismmedicine.anatomical_structureMutation (genetic algorithm)GeneticsmedicineAgronomy and Crop Sciencemedia_commonEuphytica
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