Search results for "arrangement."

showing 10 items of 343 documents

The evolution of human synteny 4 by mapping sub-chromosomal specific probes in Primates

2014

Comparative cytogenetic data concerning the orthologue to human chromosome 4 in primates shows that this chromosome is conserved between humans and non-human primates. However, the degree of conservation is not as high as previously estimated. In primates it is as a rule a large submetacentric chromosome but many exceptions are known especially in taxa characterized by a high level of chromosomal rearrangements. The rearrangements that have been visualized by chromosome painting so far, which are mostly interchromosomal changes, are in fact only a fraction of the actual chromosomal changes that have occurred during evolution. Intrachromosome changes can be analysed through classical cytogen…

GeneticsChromosome engineeringchromosomal rearrangementbiologyHuman chromosome 4; chromosomal rearrangements; Platyrrhini Phylogeny; EvolutionEvolutionHuman chromosome 4CatarrhiniChromosomePlatyrrhiniSettore BIO/08 - Antropologiabiology.organism_classificationChromosome 4Evolutionary biologyPhylogeneticsCentromereGeneticsPlatyrrhini PhylogenyGeneral Agricultural and Biological SciencesSynteny
researchProduct

Plasticity of human chromosome 3 during primate evolution.

2004

Comparative mapping of more than 100 region-specific clones from human chromosome 3 in Bornean and Sumatran orangutans, siamang gibbon, and Old and New World monkeys allowed us to reconstruct ancestral simian and hominoid chromosomes. A single paracentric inversion derives chromosome 1 of the Old World monkey Presbytis cristata from the simian ancestor. In the New World monkey Callithrix geoffroyi and siamang, the ancestor diverged on multiple chromosomes, through utilizing different breakpoints. One shared and two independent inversions derive Bornean orangutan 2 and human 3, implying that neither Bornean orangutans nor humans have conserved the ancestral chromosome form. The inversions, f…

GeneticsGene RearrangementLineage (genetic)ChromosomeChromosome MappingChromosome BreakageGene rearrangementHaplorhiniBiologySyntenyEvolution MolecularChromosome 3Evolutionary biologyGene DuplicationGeneticsAnimalsHumansChromosomes ArtificialChromosomes Human Pair 3Chromosome 21Chromosome 12PhylogenySyntenyChromosomal inversionGenomics
researchProduct

Cytogenetic manifestations associated with the reversion, by gene amplification, at the HGPRT locus in V79 Chinese hamster cells.

1989

SummarySome HGPRT spontaneous revertants were isolated from a mutant line (E2) of V79 Chinese hamster cells and phenotypically characterized. Dot–Blot hybridization with a32P-Iabelled HGPRT probe revealed an increase in the number of HGPRT sequences in some of these revertants, suggesting the occurrence of gene amplification. Cytogenetic analysis performed in three of these revertants showed a characteristic abnormally banding region (ABR) on the elongated p arm of theXchromosome.In Situhybridization in one revertant (RHE2) showed that the amplified sequences reside on the p+arm of theXchromsome in two different localizations. Because of the very probable clonal origin of the revertant, the…

GeneticsGene Rearrangementmedicine.medical_specialtyHypoxanthine PhosphoribosyltransferaseCytogeneticsReversionGene AmplificationChromosomeHamsterKaryotypeGeneral MedicineGene rearrangementBiologybiology.organism_classificationMolecular biologyChinese hamsterCell LineCricetinaeMutationGeneticsmedicineAnimalsX chromosomeGenetical research
researchProduct

Structural characterization of chromosome I size variants from a natural yeast strain

2002

Many yeast strains isolated from the wild show karyotype instability during vegetative growth, with rearrangement rates of up to 10(-2) chromosomal changes per generation. Physical isolation and analysis of several chromosome I size variants of one of these strains revealed that they differed only in their subtelomeric regions, leaving the central 150 Kb unaltered. Fine mapping of these subtelomeric variable regions revealed gross alterations of two very similar loci, FLO1 and FLO9. These loci are located on the right and left arms, respectively, of chromosome I and encompass internal repetitive DNA sequences. Furthermore, some chromosome I variants lacking the FLO1 locus showed evidence of…

GeneticsSequence analysisFungal geneticsChromosomeBioengineeringLocus (genetics)KaryotypeChromosomal rearrangementBiologySubtelomereApplied Microbiology and BiotechnologyBiochemistryGeneticsRepeated sequenceBiotechnologyYeast
researchProduct

Massive LINE-1 retrotransposon enrichment in tamarins of the Cebidae family (Platyrrhini, Primates) and its significance for genome evolution

2021

To study heterochromatin distribution differences among tamarins, we applied LINE-1 probes using fluorescence in situ hybridization onto chromosomes of Saguinus mystax, Leontocebus fuscicollis, and Leontopithecus rosalia with the aim to investigate possible evolutionary implications. LINE-1 repeats were shown to be involved in genome architecture and in the occurrence of chromosomal rearrangements in many vertebrates. We found bright LINE-1 probe signals at centromeric or pericentromeric areas, GC rich, on almost all chromosomes in three tamarin species. We also found non-centromeric signals along chromosome arms. In a phylogenetic perspective, we analyzed the pattern of LINE-1 distribution…

Genome evolutionbiologyrearrangementheterochromatinrepetitive sequencesPlatyrrhiniRetrotransposonSettore BIO/08 - Antropologiabiology.organism_classificationinversionEvolutionary biologyGeneticsCebidaeAnimal Science and ZoologyLine (text file)Molecular BiologyEcology Evolution Behavior and Systematics
researchProduct

7E olfactory receptor gene clusters and evolutionary chromosome rearrangements

2005

Olfactory receptor (OR) genes of the 7E subfamily have been duplicated to multiple regions throughout the human genome. Segmental duplications containing 7E OR genes have been associated with both pathological and evolutionary chromosome rearrangements. Many of these breakpoint regions coincide with breaks of chromosomal synteny in the mouse, rat and/or chicken genomes. Collectively, these data suggest that 7E OR-containing regions represent hot spots of genomic instability.    

Genome instabilityChromosomes Artificial BacterialGenome evolutionBiologyReceptors OdorantGenomeEvolution MolecularGene DuplicationGeneticsmedicineAnimalsHumansMolecular BiologyGeneIn Situ Hybridization FluorescenceGenetics (clinical)SyntenySegmental duplicationGene RearrangementMammalsGeneticsGenomeOlfactory receptorGenome HumanChromosome Mappingmedicine.anatomical_structureMultigene FamilyHuman genomeCytogenetic and Genome Research
researchProduct

Genome structure reveals the diversity of mating mechanisms in Saccharomyces cerevisiae x Saccharomyces kudriavzevii hybrids, and the genomic instabi…

2020

Interspecific hybridization has played an important role in the evolution of eukaryotic organisms by favouring genetic interchange between divergent lineages to generate new phenotypic diversity involved in the adaptation to new environments. This way, hybridization between Saccharomyces species, involving the fusion between their metabolic capabilities, is a recurrent adaptive strategy in industrial environments. In the present study, whole-genome sequences of natural hybrids between Saccharomyces cerevisiae and Saccharomyces kudriavzevii were obtained to unveil the mechanisms involved in the origin and evolution of hybrids, as well as the ecological and geographic contexts in which sponta…

Genome instabilitybiologyHybridization mechanismsMechanism (biology)Rare-matingSaccharomyces cerevisiaeGenome rearrangementsHybridsGeneral MedicineSaccharomyces cerevisiaebiology.organism_classificationPhenotypeEvolutionary biologyMatingAdaptationSaccharomyces kudriavzeviiSaccharomyces kudriavzeviiHybrid
researchProduct

Environmental mobility barriers and walking for errands among older people who live alone vs. with others

2013

Background. Walking is the most popular form of physical activity among older people and for community-dwelling older people walking for errands is especially important. The aim of this study is to examine the association between self-reported environmental mobility barriers and amount of walking for errands among older people who live alone compared to those who live with others. Methods. This observational study is based on cross-sectional data on 657 people aged 75–81 living in Jyväskylä, Central Finland. Self-reports of environmental mobility barriers were collected under four categories: Traffic, Terrain, Distances and Entrance. Persons who reported walking for errands ≤ 1.5 km/week or…

GerontologyMaleAgingActivities of daily livingympäristöCross-sectional studyliving arrangementsLevel designWalkingOdds03 medical and health sciences0302 clinical medicineKilometerResidence CharacteristicsActivities of Daily LivingSingle personMedicineHumans030212 general & internal medicineMobility LimitationEnvironmental barriersAgedMobilityAged 80 and overbusiness.industryagingPublic Health Environmental and Occupational HealthSingle PersonikääntyminenliikkuvuusLiving arrangementsCross-Sectional StudiesMobility Limitationliikumiskykyenvironmental barriersEnvironment DesignFemaleBiostatisticsbusinesshuman activities030217 neurology & neurosurgeryResearch ArticleBMC Public Health
researchProduct

Electrochemical Allylic Oxidation of Olefins: Sustainable and Safe.

2016

The power you're supplying: With the application of an optimized electrochemical approach, the allylic oxidation of olefins, which is an important C-H activation process that provides access to enones, becomes a sustainable, versatile, and potent key reaction for organic synthesis.

Green chemistryAllylic rearrangement010405 organic chemistryGeneral Chemistry010402 general chemistryElectrosynthesisElectrochemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundchemistryOrganic chemistryOrganic synthesisAngewandte Chemie (International ed. in English)
researchProduct

Gamma-delta T-cell lymphomas.

2009

Peripheral T-cell lymphomas (TCLs) are uncommon neoplasms, accounting for about 12% of all lymphoid tumors worldwide. TCLs in which gammadelta T-cell receptors are expressed (gammadelta TCLs) are extremely aggressive and rare (<1% of lymphoid neoplasms). gammadelta TCLs originate from gammadelta T cells, a small subset of peripheral T cells with direct antigen recognition capability acting at the interface between innate and adaptive immunity. Two distinct gammadelta TCL entities are recognized: hepatosplenic T-cell lymphoma (HSTL) and primary cutaneous gammadelta T-cell lymphoma (PCGD-TCL). HSTL is a well-characterized extranodal lymphoma that has a disguised onset, secondary to intrasinus…

Hepatosplenic T-cell lymphomaT cellGene Rearrangement delta-Chain T-Cell Antigen Receptorchemical and pharmacologic phenomenaprimary cutaneous gamma delta T-cell lymphomaImmune systemmedicineHumansGamma delta T cellLymphoma T-Cell CutaneouClinical Trials as Topicbusiness.industryGene Rearrangement gamma-Chain T-Cell Antigen Receptorgamma delta T-cell receptorMedicine (all)Peripheral T-cell lymphomaLymphoma T-Cell PeripheralReceptors Antigen T-Cell gamma-deltaGene rearrangementmedicine.diseaseAcquired immune systemLymphomaLymphoma T-Cell Cutaneousstomatognathic diseasesmedicine.anatomical_structurehepatosplenic T-cell lymphomaOncologyImmunologyBone marrowbusinessHuman
researchProduct