Search results for "Crossing Over"

showing 10 items of 10 documents

Sister-chromatid exchange in cultured lymphocytes of ewes and their newborn lambs

1984

The incidence of sister-chromatid exchange (SCE) in cultured lymphocytes of ewes and their newborn lambs was determined using the BrdU-Giemsa technique. In all ewe-lamb pairs, the SCE rate in the lambs was less than that of the ewes. The mean SCE frequencies per chromosome of the ewes after lambing and of the newborn lambs were 0.1909 and 0.1581, respectively. The statistical analysis shows that a significant difference exists between SCE in the adult female sheep and their lambs. At the same time, a negative correlation was observed between SCE rate and cell proliferation. The results of this study are compared with those of previous reports on age-dependency of SCE.

AdultAgingAdolescentanimal diseasesSister chromatid exchangeBiologyAndrologyPregnancyparasitic diseasesAnimalsHumansStatistical analysisCrossing Over GeneticLymphocytesChildCells CulturedAgedGeneticsSheepAdult femaleIncidence (epidemiology)Domestic sheep reproductionSignificant differenceInfant NewbornInfantChromosomeGeneral MedicineMiddle Agedrespiratory systemAnimals NewbornChild PreschoolFemaleNegative correlationSister Chromatid ExchangeCell DivisionMutation Research Letters
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Replication of linkage of familial hypobetalipoproteinemia to chromosome 3p in six kindreds

2002

Familial hypobetalipoproteinemia (FHBL) is a genetically heterogeneous condition characterized by very low apolipoprotein B (apoB) concentrations in plasma and/or low levels of LDL-cholesterol (LDL-C) with a propensity to developing fatty liver. In a minority of cases, truncation-specifying mutations of the apoB gene (APOB) are etiologic, but the genetic basis of most cases is unknown. We previously reported linkage of FHBL to a 10 cM region on 3p21.1-22 in one kindred. The objectives of the current study were to identify other FHBL families with linkage to 3p and to narrow the FHBL susceptibility region on 3p. Six additional FHBL kindreds unlinked to the APOB region on chromosome 2 were ge…

Genetic MarkersAdultMaleMeiosiSettore MED/09 - Medicina InternaApolipoprotein BGenotypeGenetic LinkageQD415-436BiologyBiochemistryChromosomal crossoverHypobetalipoproteinemiasEndocrinologyQuantitative Trait HeritableGenetic linkageGenetic MarkerHaplotypeHumanslinkage analysisCrossing Over GeneticChildAgedAdult; Aged; Aged 80 and over; Child; Chromosome Mapping; Chromosomes Human Pair 3; Crossing Over Genetic; Female; Genetic Linkage; Genetic Markers; Genotype; Haplotypes; Humans; Hypobetalipoproteinemias; Male; Meiosis; Middle Aged; Pedigree; Quantitative Trait HeritableGeneticsAged 80 and overGenetic heterogeneityHaplotypeChromosomeChromosome MappingCell BiologyoligogenicMiddle AgedPedigreeMeiosisMarkov chain Monte CarloChromosome 3HaplotypesGenetic markerbiology.proteinvariance componentslipids (amino acids peptides and proteins)FemaleChromosomes Human Pair 3geneticHypobetalipoproteinemiaHuman
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Infectious transfer of a fertility factor inStreptomyces coelicolor

1973

SUMMARYInitial Fertility (IF) strains ofStreptomyces coelicolorare able to convert recipient strains (UF) to the IF condition by contact, without concomitant transfer of chromosomal markers. The conversion is prevented by the presence of acridine orange in the medium of the mixed culture. Acridine orange is also moderately effective in inducing the formation of UF variants from IF-treated strains. No effect of the drug is observed on UF variant formation from Normal Fertility (NF) strains nor on the behaviour of the fertility factor in NF × UF mixed cultures. The hypothesis is put forward that the fertility factor works as an episome inS. coelicolor, fixed to the chromosome in the NF strain…

Genetics MicrobialGeneticsFertility factor (bacteria)biologymedia_common.quotation_subjectStreptomyces coelicolorAcridine orangeChromosomeFertilityGeneral MedicineNormal fertilitybiology.organism_classificationStreptomyceschemistry.chemical_compoundFertilitychemistryMixed cultureGeneticsCrossing Over GeneticAllelesmedia_commonGenetical Research
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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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Mechanism for polarized recombination in Streptomyces.

1968

Recombination between pairs of mutations in a cluster of seven cistrons controlling histidine biosynthesis is highly polarized. The polarity is opposite at the opposite ends of the region. In experiments involving three his mutations it has been shown that recombination is the result of the transfer, from one parent to the other, of a segment going from the distal selected his+ allele to the end of the region. The rate of transfer is inversely proportional to the distance of the transferred his+ allele from the end of the region, at its side. A model of the process of recombination is discussed.

GeneticsRecombination GeneticPolarity (international relations)biologyStereochemistryChromosome MappingHistidine biosynthesisbiology.organism_classificationStreptomycesModels BiologicalStreptomycesGeneticsHistidineCrossing Over GeneticAlleleMolecular BiologyRecombinationHistidineCrosses GeneticMoleculargeneral genetics : MGG
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SRC1: an intron-containing yeast gene involved in sister chromatid segregation

2001

Analysis of a three-member gene family in the yeast Saccharomyces cerevisiae has allowed the discovery of a new gene that comprises two contiguous open reading frames previously annotated as YML034w and YML033w. The gene contains a small intron with two alternative 5′ splicing sites. It is specifically transcribed during G2/M in the cell cycle and after several hours of meiosis induction. Splicing of the mRNA is partially dependent on NAM8 but does not vary during meiosis or the cell cycle. Deletion of the gene induces a shortening of the anaphase and aggravates the phenotype of scc1 and esp1 conditional mutants, which suggests a direct role of the protein in sister chromatid separation. Co…

GeneticsUnequal crossing overbiologySaccharomyces cerevisiaeIntronBioengineeringbiology.organism_classificationApplied Microbiology and BiotechnologyBiochemistrySister chromatid segregationEstablishment of sister chromatid cohesionGeneticsGene familySister chromatidsGeneBiotechnologyYeast
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Copy-number fluctuation by unequal crossing-over in the chicken avidin gene family.

2001

The chicken avidin gene (AVD) forms a closely clustered gene family together with several avidin-related genes (AVRs). In this study, we used fluorescence in situ hybridization on extended DNA fibers (fiber-FISH) to show that the number of the AVD and AVR genes differs between individuals. Furthermore, the gene copy-number showed wide somatic variation in white blood cells of the individuals. The molecular mechanism underlying the fluctuation is most probably unequal crossing-over and/or unequal sister chromatid exchange, as judged by the Gaussian distribution of the gene counts. By definition, an increase in gene number on one locus should be accompanied by a decrease on the other locus in…

GeneticsUnequal crossing overmedicine.diagnostic_testBiophysicsGene DosageLocus (genetics)Cell BiologyBiologyAvidinBiochemistryMultigene FamilyGene clustermedicinebiology.proteinGene familyAnimalsGene conversionCrossing Over GeneticMolecular BiologyGeneChickensIn Situ Hybridization FluorescenceFluorescence in situ hybridizationAvidinBiochemical and biophysical research communications
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Meiosis in translocation heterozygotes in the mosquito Culex pipiens.

1971

Adult Culex pipiens males irradiated with both X-rays and neutrons were crossed to untreated females and F1-egg rafts were checked for dominant lethality. F1-progenies were outcrossed with normal individuals in order to obtain lines with inherited semisterility. From a total of 120 lines that showed a certain amount of sterility 12 lines were studied cytologically. 10 lines showed reciprocal chromosome exchanges.—At late pachytene and diplotene cross configurations with large asynaptic regions at the center of the cross are obligatory. Bivalents, chains of three, chains of four, and ring configurations are present at metaphase and anaphase I. The different frequencies of the occurrence of s…

MaleHeterozygoteBiometryMitosisInterference (genetic)ChromosomesMeiosisCulex pipiensCentromereGeneticsAnimalsCrossing Over GeneticMetaphaseGenetics (clinical)Crosses GeneticAnaphaseGenes DominantGeneticsChromosome AberrationsNeutronsbiologyChromosomebiology.organism_classificationChiasmaRadiation EffectsCulexMeiosisInfertilityFemaleGenes LethalChromosoma
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Repeat expansion in spinocerebellar ataxia type 17 alleles of the TATA-box binding protein gene: an evolutionary approach.

2006

The variability and mutational changes of the CAG microsatellite in the TATA-box binding protein gene (TBP) were studied. We sequenced the microsatellite of the TBP gene of 25 unrelated individuals from northern Germany (10 SCA17 patients and 15 unaffected control individuals). In addition, the microsatellites were sequenced from individuals of 10 northern German families with at least one family member affected by SCA17. To study also the evolutionary history of this CAG/CAA microsatellite in nonhuman primates, the homologous regions were analysed from Pan troglodytes, Gorilla gorilla, Pongo pygmaeus, P. abellii, Hylobates lar, Nomascus leucogenys, Symphalangus syndactylus, Macaca mulatta,…

MalePrimatesUnequal crossing overEvolution MolecularMolecular evolutionHylobatesGeneticsmedicineAnimalsHumansSpinocerebellar AtaxiasComputer SimulationAlleleGenetics (clinical)GeneticsbiologyGenetic Variationbiology.organism_classificationmedicine.diseaseTATA-Box Binding ProteinNomascus leucogenysSpinocerebellar ataxiaMicrosatelliteFemaleTrinucleotide repeat expansionTrinucleotide Repeat ExpansionEuropean journal of human genetics : EJHG
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Metabolites of diethylstilboestrol induce sister chromatid exchange in human cultured fibroblasts

1979

Diethylstilboesterol (DES) is one of the few substances for which a clear association with carcinogenicity has been established in man. Nevertheless, it is still widely used, mainly as a cheap oestrogen to increase the slaughter weight of beef, but in spite of this it is not known if residues in the meat or metabolites excreted by the cattle are hazardous to man. It is also unknown whether there is a threshold dose below which DES is harmless. A threshold might be expected if a hormonal mechanism of carcinogensis rather than metabolic activation to an electrophically reactive species operats. This possibility was supported by the observations that DES, in contrast to most other carcinogens,…

Salmonella typhimuriumSalmonellaMultidisciplinaryChemistrySister chromatid exchangeStimulationNaphtholsmedicine.disease_causeSlaughter weightStimulation ChemicalMixed Function OxygenasesThreshold doseBiochemistryMutationmedicineMicrosomeHumansCrossing Over GeneticDiethylstilbestrolSister Chromatid ExchangeCells CulturedCarcinogenHormoneNature
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