Search results for "VARIATION"

showing 10 items of 2124 documents

Genetic divergence between morphological forms of brown troutSalmo truttaL. in the Balkan region of Macedonia

2010

The objective of this study was to characterize the genetic structure of two Balkan brown trout morphotypes, Salmo macedonicus and Salmo pelagonicus, and to test whether molecular traits support the species’ status proposed by traditional morphological identification. The mitochondrial DNA 12S-rDNA, cyt b and control region genes were sequenced in 15 specimens collected from three localities in the Former Yugoslav Republic of Macedonia. The results of these markers did not support the taxonomic category of species but confirmed the existence of two morphotypes, Salmo trutta macedonicus and Salmo trutta pelagonicus, in the Aegean–Adriatic lineages of the Salmo trutta species complex.

Mitochondrial DNASpecies complexTroutanimal diseasesSettore BIO/05 - ZoologiaZoologyAquatic ScienceDNA MitochondrialBrown troutSalmo truttaAnimalsCluster AnalysisSalmomorphotypemtDNA.PhylogenyEcology Evolution Behavior and SystematicsbiologyEcologyCytochrome bGenetic VariationSequence Analysis DNAbiology.organism_classificationSalmo macedonicusEuropeGenetic divergenceGenetics PopulationFormer Yugoslav Republic of Macedonia (FYRM)HaplotypesGenetic structureJournal of Fish Biology
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Human paleogenetics of Europe--the known knowns and the known unknowns.

2014

The number of ancient human DNA studies has drastically increased in recent years. This results in a substantial record of mitochondrial sequences available from many prehistoric sites across Western Eurasia, but also growing Y-chromosome and autosomal sequence data. We review the current state of research with specific emphasis on the Holocene population events that likely have shaped the present-day genetic variation in Europe. We reconcile observations from the genetic data with hypotheses about the peopling and settlement history from anthropology and archaeology for various key regions, and also discuss the data in light of evidence from related disciplines, such as modern human geneti…

Mitochondrial DNAeducation.field_of_studyPopulationPaleogeneticsGenetic VariationPaleontologyDNADNA MitochondrialHuman geneticsPrehistoryEuropePaleontologyGeographyAncient DNAArchaeologyEvolutionary biologyAnthropologyChromosomes HumanHumanseducationEcology Evolution Behavior and SystematicsHoloceneMesolithicJournal of human evolution
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Ancient DNA Reveals Key Stages in the Formation of Central European Mitochondrial Genetic Diversity

2013

The Origins of Europeans To investigate the genetic origins of modern Europeans, Brandt et al. (p. 257 ) examined ancient mitochondrial DNA (mtDNA) and were able to identify genetic differences in 364 Central Europeans spanning the early Neolithic to the Early Bronze Age. Observed changes in mitochondrial haplotypes corresponded with hypothesized human migration across Eurasia and revealed the complexity of the demographic changes and evidence of a Late Neolithic origin for the European mtDNA gene pool. This transect through time reveals four key population events associated with well-known archaeological cultures, which involved genetic influx into Central Europe from various directions at…

Mitochondrial DNAmedia_common.quotation_subjectMolecular Sequence DataPopulationPopulationBiologyDNA MitochondrialArticleGenetic driftBronze AgeGenetic variationHumanseducationHistory Ancientmedia_commonTransients and MigrantsGeneticseducation.field_of_studyGenetic diversityMultidisciplinaryBase SequenceGenetic DriftGenetic VariationAgricultureEuropeAncient DNAEvolutionary biologyDiversity (politics)Science
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Diachronic variation in the Middle Paleolithic settlement of Abrigo de la Quebrada (Chelva, Spain)

2017

Abstract This paper compares levels IV and VIII of Abrigo de la Quebrada. The study includes knapping technique, raw material, fauna, and the spatial distribution of lithic and bone remains. Although both levels correspond to cumulative palimpsests, patterns of resource management and use of space that suggest changes in the rhythm of occupation and the functionality of the settlements can be discerned. A change in mobility patterns probably underpins the differences between these two levels of Quebrada, but assessing this hypothesis is made difficult by the lack of comparable documentation for other sites in the region.

Mobility010506 paleontologySettlement060102 archaeologyKnappingFaunaSpatial analysis06 humanities and the artsSpatial distribution01 natural sciencesArchaeologyVariation (linguistics)GeographyMiddle PaleolithicHuman settlementMiddle Palaeolithic0601 history and archaeologySettlement (litigation)0105 earth and related environmental sciencesEarth-Surface Processes
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Isolation and Characterization of Two Klebsiella pneumoniae Phages Encoding Divergent Depolymerases

2020

The emergence of multidrug-resistant bacteria is a major global health concern. The search for new therapies has brought bacteriophages into the spotlight, and new phages are being described as possible therapeutic agents. Among the bacteria that are most extensively resistant to current antibiotics is Klebsiella pneumoniae, whose hypervariable extracellular capsule makes treatment particularly difficult. Here, we describe two new K. pneumoniae phages, &pi

Models Molecular0301 basic medicineKlebsiellaPhage therapyKlebsiella pneumoniae<i>Klebsiella pneumoniae</i>virusesmedicine.medical_treatmentAntibioticsMolecular Conformationlcsh:ChemistryBacteriophagebacteriophagewide infection rangeBacteriophagesAntigens Virallcsh:QH301-705.5PhylogenySpectroscopybiologyGeneral Medicine3. Good healthComputer Science ApplicationsKlebsiella pneumoniaePhenotypephage therapyPhage therapymedicine.drug_class030106 microbiologyGenome ViralArticleHost SpecificityCatalysisMicrobiologyInorganic ChemistryViral Proteins03 medical and health sciencesPodoviridaeBacteriolysismedicineAmino Acid SequencePhysical and Theoretical ChemistryBacteriophageMolecular BiologyTropismWhole Genome SequencingOrganic ChemistryComputational BiologyGenetic VariationMolecular Sequence Annotationbiology.organism_classificationKlebsiella Infections030104 developmental biologylcsh:Biology (General)lcsh:QD1-999Wide infection rangeBacteriaInternational Journal of Molecular Sciences
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Molecular evolutionary analysis of type-1 human astroviruses identifies putative sites under selection pressure on the capsid protein

2017

Human astroviruses (HAstV) are important enteric pathogens that can be classified into eight sero/genotypes (HAstV-1 to -8). Although the various HAstV types show global spread, type-1 strains tend to be predominant. Molecular analysis of the genomic region encoding the capsid protein (ORF2) has revealed discrete sequence variation, with different lineages within each HAstV type and at least three major lineages have been identified within HAstV-1. Longitudinal epidemiological surveillance has revealed temporal shift of the various HAstV-1 lineages. Metadata analysis of HAstV-1 sequences available in the databases also revealed temporal shifts of the circulation of HAstV-1 lineages, suggest…

Models Molecular0301 basic medicineMicrobiology (medical)Settore MED/07 - Microbiologia E Microbiologia ClinicaGenotypeProtein ConformationAstroviru030106 microbiologyBiologyMicrobiologyAstrovirusEvolution MolecularOpen Reading Frames03 medical and health sciencesProtein structureGeneticPhylogeneticsAstroviridae InfectionsGenetic variationGenotypePhylogenetic analyseGeneticsHumansAmino Acid SequenceSelection GeneticPeptide sequenceMolecular BiologyPhylogenyEcology Evolution Behavior and SystematicsGeneticsGenetic evolutionSelection pressure analysiGenetic Variationbiology.organism_classificationEcology Evolution Behavior and SystematicOpen reading frame030104 developmental biologyInfectious DiseasesCapsidAstroviridaeCapsid ProteinsCapsid protein structureHAstV-1
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Diversity of Omega Glutathione Transferases in mushroom-forming fungi revealed by phylogenetic, transcriptomic, biochemical and structural approaches

2021

International audience; The Omega class of glutathione transferases (GSTs) forms a distinct class within the cytosolic GST superfamily because most of them possess a catalytic cysteine residue. The human GST Omega 1 isoform was first characterized twenty years ago, but it took years of work to clarify the roles of the human isoforms. Concerning the kingdom of fungi, little is known about the cellular functions of Omega glutathione transferases (GSTOs), although they are widely represented in some of these organisms. In this study, we re-assess the phylogeny and the classification of GSTOs based on 240 genomes of mushroom-forming fungi (Agaricomycetes). We observe that the number of GSTOs is…

Models MolecularGene isoformProtein ConformationCrystallography X-RayMicrobiologyAgaricomycetesstructure-functionFungal ProteinsSerine03 medical and health scienceschemistry.chemical_compoundPhylogeneticsGeneticsPolyporalesflavonoid[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyglutathionePhylogeny[SDV.MP.MYC]Life Sciences [q-bio]/Microbiology and Parasitology/MycologyGlutathione Transferase030304 developmental biologychemistry.chemical_classification0303 health sciencesBinding Sitesbiology030306 microbiologyGene Expression ProfilingGenetic VariationGlutathionebiology.organism_classificationenzymeEnzymeBiochemistrychemistryfungi[SDE.BE]Environmental Sciences/Biodiversity and EcologyAgaricalesCysteine[SDV.EE.IEO]Life Sciences [q-bio]/Ecology environment/Symbiosis
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Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis.

2006

Variation in major histocompatibility complex genes on chromosome 6p21.3, specifically the human leukocyte antigen HLA-DR2 or DRB1*1501-DQB1*0602 extended haplotype, confers risk for multiple sclerosis (MS). Previous studies of DRB1 variation and both MS susceptibility and phenotypic expression have lacked statistical power to detect modest genotypic influences, and have demonstrated conflicting results. Results derived from analyses of 1339 MS families indicate DRB1 variation influences MS susceptibility in a complex manner. DRB1*15 was strongly associated in families (P=7.8x10(-31)), and a dominant DRB1*15 dose effect was confirmed (OR=7.5, 95% CI=4.4-13.0, P<0.0001). A modest dose effect…

Models MolecularMaleSequence Homologyimmune system diseasesModelsRisk FactorsDatabases GeneticAdult Alleles Amino Acid Sequence Databases; Genetic Female Genetic Variation Genotype HLA-DR Antigens; chemistry/genetics HLA-DRB1 Chains Humans Male Middle Aged Models; Molecular Molecular Sequence Data Multiple Sclerosis; Chronic Progressive; genetics/immunology Multiple Sclerosis; genetics/immunology Phenotype Risk Factors Sequence Homology; Amino Acidskin and connective tissue diseasesHLA-DRB1Genetics (clinical)GeneticsGeneral MedicineMultiple Sclerosis Chronic ProgressiveMiddle AgedAmino AcidChronic ProgressivePhenotypeFemalemusculoskeletal diseasesAdultMultiple SclerosisGenotypeMolecular Sequence DataLocus (genetics)Human leukocyte antigenBiologyDatabases. Alleles phenotype heterogeneity human leukocyte antigens age of onset chromosomes genes genotype haplotypesmultiple sclerosis relapsing-remitting genetics disability primary progressive multiple sclerosis hla-drb1 gene illness length severity of illnessGeneticGenetic variationGeneticsmedicineHumansAmino Acid SequenceAlleleMolecular BiologyAllelesSequence Homology Amino AcidMultiple sclerosisHaplotypeGenetic VariationMolecularHLA-DR Antigensmedicine.diseasegenetics/immunologychemistry/geneticsImmunologyAge of onsetHLA-DRB1 Chains
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Mutational analysis of disulfide bonds in the trypsin-reactive subdomain of a Bowman-Birk-type inhibitor of trypsin and chymotrypsin--cooperative ver…

1998

It is widely believed that protein folding is a hierarchical process proceeding from secondary structure via subdomains and domains towards the complete tertiary structure. Accordingly, protein subdomains should behave as independent folding units. However, this prediction would underestimate the well-established structural significance of tertiary context and domain interfaces in proteins. The principal objective of this work was to distinguish between autonomous and cooperative refolding of protein subdomains by means of mutational analysis. The double-headed Bowman-Birk inhibitor of trypsin and chymotrypsin of known crystal structure was selected for study. The relative orientation of th…

Models MolecularProtein FoldingProtein ConformationTrypsin inhibitorMolecular Sequence DataContext (language use)BiochemistryProtein Structure SecondaryProtein structureDrug StabilityEscherichia coliChymotrypsinTrypsinAmino Acid SequenceDisulfidesCloning MolecularProtein secondary structureTrypsin Inhibitor Bowman-Birk SoybeanChymotrypsinbiologyBase SequenceChemistryGenetic VariationDNAProtein tertiary structureRecombinant ProteinsProtein Structure TertiaryFolding (chemistry)Crystallographybiology.proteinBiophysicsMutagenesis Site-DirectedProtein foldingEuropean journal of biochemistry
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Self-organized modularization in evolutionary algorithms.

2005

The principle of modularization has proven to be extremely successful in the field of technical applications and particularly for Software Engineering purposes. The question to be answered within the present article is whether mechanisms can also be identified within the framework of Evolutionary Computation that cause a modularization of solutions. We will concentrate on processes, where modularization results only from the typical evolutionary operators, i.e. selection and variation by recombination and mutation (and not, e.g., from special modularization operators). This is what we call Self-Organized Modularization. Based on a combination of two formalizations by Radcliffe and Altenber…

Modularity (networks)education.field_of_studyTheoretical computer scienceComputer sciencebusiness.industryPopulationEvolutionary algorithmVariation (game tree)Modular designModels TheoreticalBiological EvolutionEvolutionary computationField (computer science)Computational MathematicsRange (mathematics)MutationArtificial intelligencebusinesseducationAlgorithmsEvolutionary computation
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