Search results for "PLOT"

showing 10 items of 830 documents

Chloroplast DNA and isozyme evidence on the evolution ofSenecio vulgaris (Asteraceae)

1997

Chloroplast DNA (cpDNA) and isozyme variation were analyzed over a range of populations of two infraspecific taxa of the tetraploidSenecio vulgaris. The isozyme data were supportive of the hypothesis that the weedy and cosmopolitanS. vulgaris var.vulgaris is an evolutionary derivative ofS. vulgaris subsp.denticulatus from the coasts of W Europe and montane altitudes in S Spain and Sicily. The two taxa exhibited a very high genetic identity with subsp.denticulatus containing slightly more isozyme diversity than was found in var.vulgaris. — Three cpDNA haplotypes (A, B, C) already known from other Mediterranean diploid species ofSenecio were resolved in var.vulgaris, and an additional fourth …

Genetic diversityChloroplast DNAbiologyChloroplast captureRange (biology)BotanyHaplotypeSenecio vulgarisIntrogressionPlant SciencePloidybiology.organism_classificationEcology Evolution Behavior and SystematicsPlant Systematics and Evolution
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The origin of the serpentine endemic Minuartia laricifolia subsp. ophiolitica by vicariance and competitive exclusion.

2013

Serpentine soils harbour a unique flora that is rich in endemics. We examined the evolution of serpentine endemism in Minuartia laricifolia, which has two ecologically distinct subspecies with disjunct distributions: subsp. laricifolia on siliceous rocks in the western Alps and eastern Pyrenees and subsp. ophiolitica on serpentine in the northern Apennines. We analysed AFLPs and chloroplast sequences from 30 populations to examine their relationships and how their current distributions and ecologies were influenced by Quaternary climatic changes. Minuartia laricifolia was divided into four groups with a BAPS cluster analysis of the AFLP data, one group consisted only of subsp. ophiolitica, …

Genetic diversityChloroplastsBase SequenceEcologyMolecular Sequence DataPopulationDNA ChloroplastGenetic VariationCaryophyllaceaeDisjunctBiologySubspeciesSecologanin Tryptamine AlkaloidsEvolution MolecularPhylogeographyHaplotypesSerpentine soilGeneticsVicarianceBiological dispersalAmplified Fragment Length Polymorphism AnalysisEndemismEcology Evolution Behavior and SystematicsEcosystemPhylogenyMolecular ecology
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Range Shifts of Mouse Lemurs in South-Eastern Madagascar: Evidence from Mitochondrial Genetic Data

2012

The gray mouse lemur, Microcebus murinus, occurs mainly in dry forests in western Madagascar, but its distribution extends into humid littoral forests in the south-eastern Anosy Region. We sequenced the mitochondrial hypervariable region 1 for 282 M. murinus individuals from 13 south-eastern study sites. The spatial distribution of mitochondrial haplotypes and the varying genetic distances within two haplotype clades indicated a trend of decreasing genetic diversity towards the south-eastern margin of the range. Rufous mouse lemurs, Microcebus cf. rufus, have a complementary distribution in south-eastern Madagascar which does not overlap with that of M. murinus. Taken together, the spatial …

Genetic diversityMicrocebus murinusMouse lemurbiologybiology.animalHaplotypeLittoral zoneLemurZoologybiology.organism_classificationSpatial distributionHypervariable region
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Genetic Variability and Phylogenetic Relationships within Trypanosoma cruzi I Isolated in Colombia Based on Miniexon Gene Sequences

2010

Phylogenetic studies ofTrypanosoma cruzihave identified the existence of two groups:T. cruziI andT. cruziII. There are aspects that still remain unknown about the genetic variability within theT. cruziI group. Given its epidemiological importance, it is necessary to have a better understanding ofT. cruzitransmission cycles. Our purpose was to corroborate the existence of haplotypes within theT. cruziI group and to describe the genetic variability and phylogenetic relationships, based on single nucleotide polymorphisms (SNPs) found in the miniexon gene intergenic region, for the isolates from different hosts and epidemiological transmission cycles in Colombian regions. 31T. cruziisolates wer…

Genetics0303 health sciencesMolecular epidemiologyPhylogenetic treebiologyArticle Subject030231 tropical medicineHaplotypebiology.organism_classificationlcsh:Infectious and parasitic diseases03 medical and health sciences0302 clinical medicineInfectious DiseasesPhylogeneticsGenetic variationparasitic diseaseslcsh:RC109-216ParasitologySylvatic cycleGenetic variabilityTrypanosoma cruziResearch Article030304 developmental biologyJournal of Parasitology Research
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Association of JAK-STAT pathway related genes with lymphoma risk: results of a European case-control study (EpiLymph)

2011

Previous studies have suggested an important role for the Janus kinase-signal transducer and activator of transcription (JAK-STAT) signalling pathway in tumour development. Therefore, we explored genetic variants in JAK-STAT pathway associated genes with lymphoma risk. In samples of the EpiLymph case-control study we genotyped 1536 single nucleotide polymorphisms (SNPs) using GoldenGate BeadArray™ Technology (Illumina, San Diego, CA, USA). Here, we report the associations between selected SNPs and haplotypes of the JAK-STAT pathway and risk of Hodgkin lymphoma (HL), B-cell non-Hodgkin lymphoma (B-NHL) and most frequent B-NHL subtypes. Among 210 relevant JAK-STAT pathway-related SNPs, polymo…

Genetics0303 health sciencesmedicine.medical_specialtyHematologyHaplotypeJAK-STAT signaling pathwaySingle-nucleotide polymorphismHematologyBiologymedicine.diseaseLymphomaSTAT5A03 medical and health sciences0302 clinical medicineimmune system diseaseshemic and lymphatic diseases030220 oncology & carcinogenesisInternal medicineIL12ACancer researchmedicineSNP030304 developmental biologyBritish Journal of Haematology
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Immunogenetics of longevity. Is major histocompatibility complex polymorphism relevant to the control of human longevity? A review of literature data.

2001

Literature data suggest that human longevity may be directly correlated with optimal functioning of the immune system. Therefore, it is likely that one of the genetic determinants of longevity resides in those polymorphisms for the immune system genes that regulate immune responses. Accordingly, studies performed on mice have suggested that the Major Histocompatibility Complex (MHC), known to control a variety of immune functions, is associated with the life span of the strains. In the last 25 years, a fair number of cross-sectional studies that searched for the role of HLA (the human MHC) genes on human longevity by comparing HLA antigen frequencies between groups of young and elderly pers…

GeneticsAgingPolymorphism Geneticmedia_common.quotation_subjectHaplotypeLongevityLongevityHuman leukocyte antigenImmunogeneticsBiologyMajor histocompatibility complexHistocompatibilityMajor Histocompatibility ComplexMiceImmune systemAntigenHLA AntigensImmunologybiology.proteinImmunogeneticsAnimalsHumansGenetic Predisposition to DiseaseDevelopmental Biologymedia_commonMechanisms of ageing and development
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Phylogeography of the Eurasian Willow Tit (Parus montanus) based on DNA sequences of the mitochondrial cytochrome b gene.

2002

The phylogeographic relationships of the trans-Palearctic Willow Tit assemblage were studied by obtaining sequence data from the mitochondrial cytochrome b gene from 34 specimens representing nine subspecies from across the species range. Four distinct genetic groups were identified: Parus montanus weigoldicus, P. m. affinis, P. m. songarus, and a clade containing six Eurasian subspecies (ssp. baicalensis, borealis, montanus, restrictus, rhenanus, and sachalinensis). P. m. weigoldicus, P. m. affinis, and P. m. songarus were reciprocally monophyletic and separated from each other and other subspecies by uncorrected genetic distances between 1.9 and 5.8%. The remaining six subspecies were clo…

GeneticsAsiaSpecies distributionZoologyGenetic VariationSubspeciesBiologybiology.organism_classificationCytochrome b GroupDNA MitochondrialBirdsEuropeMonophylyPhylogeographyWillow titHaplotypesPhylogeneticsMolecular phylogeneticsGeneticsAnimalsCladeMolecular BiologyEcology Evolution Behavior and SystematicsPhylogenyMolecular phylogenetics and evolution
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Mapping of Friedreich's ataxia locus by identification of recombination events in patients homozygous by descent

1994

The Friedreich's ataxia locus (FRDA) maps on chromosome 9q13. Genetic data, obtained from a small number of recombination events, indicated that the FRDA locus might be located centromeric to the D9S15/D9S5 linkage group, the most probable order being cen-FRDA-D9S5-D9S111-D9S15-D9S110-qter. Recently, new centromeric markers have been reported. Analysis of these markers allowed us to localize the recombination breakpoint in some of the recombinant families. However, only one proximal recombination has been found with these markers. To increase the genetic information from FRDA families, we have analyzed the centromeric markers FR1, FR2, FR7, FR8, and FR5 in patients homozygous by descent. Th…

GeneticsAtaxiaConsanguineous familyHaplotypeCentromereGenetic dataChromosome MappingLocus (genetics)BiologyPedigreeMeiosisFriedreich AtaxiaGeneticsmedicineHumansIn patientmedicine.symptomChromosomes Human Pair 9Genetics (clinical)RecombinationBiomarkers
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Mitochondrial DNA evolution in experimental populations of Drosophila subobscura.

1990

When two mitochondrial DNA (mtDNA) haplotypes of Drosophila subobscura compete in experimental populations with discrete generations, one or the other approaches fixation, depending on the nuclear background with which they are associated. The approach to fixation, however, is strongly dependent on the effective number of females in the population, Nf. Whether or not the ultimate fate of a given mtDNA haplotype is determined by random genetic drift depends on Nf as well as on the relative fitnesses. Our experimental results show that the mtDNA polymorphisms observed in natural populations are affected by interactions among nuclear polymorphisms, random genetic drift, and direct selection on…

GeneticsCell NucleusMitochondrial DNAeducation.field_of_studyMultidisciplinaryHaplotypePopulationPopulation geneticsGenetic VariationBiologyBiological EvolutionDNA MitochondrialDrosophila subobscuraFixation (population genetics)Genetics PopulationGenetic driftHaplotypesEvolutionary biologyGenetic variationChromosome InversionAnimalsDrosophilaeducationResearch Article
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Coat colours in the Massese sheep breed are associated with mutations in the agouti signalling protein (ASIP) and melanocortin 1 receptor (MC1R) genes

2012

Massese is an Italian dairy sheep breed characterized by animals with black skin and horns and black or apparent grey hairs. Owing to the presence of these two coat colour types, this breed can be considered an interesting model to evaluate the effects of coat colour gene polymorphisms on this phenotypic trait. Two main loci have been already shown to affect coat colour in sheep: Agouti and Extension coding for the agouti signalling protein (ASIP) and melanocortin 1 receptor (MC1R) genes, respectively. The Agouti locus is affected by a large duplication including the ASIP gene that may determine the Agouti white and tan allele (A(Wt)). Other disrupting or partially inactivating mutations ha…

GeneticsCoatsheepHaplotypeLocus (genetics)coat colour sheep ASIP MC1R mutationsBiologymutationsSF1-1100Animal cultureMASSESEExonSettore AGR/17 - Zootecnica Generale E Miglioramento GeneticoCOAT COLOURASIPGene duplicationMC1RAnimal Science and ZoologyAlleleSHEEP BREEDGeneMelanocortin 1 receptor
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