Search results for "ROSA"

showing 10 items of 1013 documents

2015

Small and isolated populations usually exhibit low levels of genetic variability, and thus, they are expected to have a lower capacity to adapt to changes in environmental conditions, such as exposure to pathogens and parasites. Comparing the genetic variability of selectively neutral versus functional loci allows one to assess the evolutionary history of populations and their future evolutionary potential. The genes of the major histocompatibility complex (MHC) control immune recognition of parasites, and their unusually high diversity is genes which is likely driven by parasite-mediated balancing selection. Here, we examined diversity and differentiation of neutral microsatellite loci and…

GeneticsGenetic diversityEcologyMHC Class I GeneZoologyBiologyMajor histocompatibility complexBalancing selectionGenetic structurebiology.proteinMicrosatelliteGenetic variabilityGeneEcology Evolution Behavior and SystematicsNature and Landscape ConservationEcology and Evolution
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Genetic diversity and clonal variation within the main Sicilian olive cultivars based on morphological traits and microsatellite markers

2014

The richness of Olea europaea (L.) genetic resources in Sicily is well documented. In the last 30 years, mostof the local cultivars, landraces and ecotypes have been gathered together in a large ex-situ collection,containing more than 300 genotypes. In this study, 45 putative clones of the main Sicilian olive cultivarswere characterized morphologically using microsatellite markers to unambiguously identify possiblesuperior genotypes. The microsatellites employed were polymorphic (observed heterozygosity = 0.71;polymorphic information content = 0.59), discriminated 52% of the genotypes and enabled the detectionof intra-cultivar polymorphism, derived from both somatic mutations, indicating th…

GeneticsGenetic diversityEcotypeUPGMAfood and beveragesHorticultureBiologyOliveOlea europaea SSR Clonal selection MicrosatellitesSettore AGR/03 - Arboricoltura Generale E Coltivazioni ArboreeGenotypeMicrosatelliteMantel testGenetic variabilityCultivarScientia Horticulturae
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Chimerism and genetic diversity within the cultivar group of pinots

2002

Three clones of Vitis vinifera cv. pinot gris were analysed at 50 microsatellite loci to assess the presence of intra-varietal genetic variability. Two clones revealed a polymorphism expressed by the presence of three alleles at 5 loci instead of the two expected for a diploid species. By sequencing the three alleles amplified at two loci, we confirm that they correspond to different allelic states of the same locus but differ in their number of repeat units. Such tri-allelic profiles could reveal periclinal chimeras in which the two cell layers of the apical meristem are genetically different. For two clones, this periclinal chimeric state has been deduced from the comparison of the genoty…

GeneticsGenetic diversity[SDV]Life Sciences [q-bio]05 social sciencesGENETICSelfingLocus (genetics)MICROSATELLITE POLYMORPHISM04 agricultural and veterinary sciencesHorticultureBiologyCHIMERISMGENETIQUE040401 food science[SDV] Life Sciences [q-bio]0404 agricultural biotechnologyPINOT GRIS0502 economics and businessGenotypeMicrosatellite050211 marketingGenetic variabilityAllelePloidyComputingMilieux_MISCELLANEOUS
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Development of retrotransposon-based SSAP molecular marker system for study of genetic diversity in sea holly (Eryngium maritimum L.)

2010

Eryngium maritimum L. is a wild plant species threatened or endangered in most of Northern Europe, where species is on the northern margin of its distribution range. Recent studies have found reduction of size and even extinction of many populations. Assessment of genetic diversity in natural populations of endangered wild plant species can reflect condition and fitness of particular population and inform decisions on appropriate conservation measures. Application of inter simple sequence repeat markers and chloroplast DNA sequencing could not resolve genetic relationship between E. maritimum populations in Northern Europe. Therefore, the more sensitive retrotransposon-sequence-specific amp…

GeneticsGenetic diversityeducation.field_of_studybiologyPopulationEndangered speciesPlant ScienceEryngium maritimumbiology.organism_classificationchemistry.chemical_compoundchemistryGenetic markerMolecular markerThreatened speciesGeneticsMicrosatelliteeducationAgronomy and Crop SciencePlant Genetic Resources
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Morphological characteristics, microsatellite fingerprinting and determination of incompatibility genotypes of Sicilian sweet cherry cultivars

2007

Sicily has extensive germplasm of diploid sweet cherry (Prunus avium L.) that has not been well studied. In this investigation, 39 cherry accessions, selected from collections and farms, were analysed using molecular markers and characterised for various morphological and other agronomic characters such as flesh colour, fruit size, quality and, in some cases, ripening periods. Thirteen Simple Sequence Repeat (SSR) primer pairs, as well as two primer pairs for the incompatibility (S) locus, which amplified across the first intron of the S-RNase gene and across the intron of the SFB gene, were used in three multiplexed reactions to analyse the accessions. The number of alleles per SSR locus r…

GeneticsGermplasmfood and beveragesLocus (genetics)Sicily sweet cherry morphologycal caractersHorticultureBiologySettore AGR/03 - Arboricoltura Generale E Coltivazioni ArboreePrunusGenotypeGeneticsMicrosatelliteCultivarAllelePloidy
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Localization of MRX82: A new nonsyndromic X-linked mental retardation locus to Xq24-q25 in a Basque family

2004

Clinical and molecular studies are reported on a Basque family (MRX82) with nonsyndromic X-linked mental retardation (XLMR) in five affected males. A total of 38 microsatellite markers were typed. The XLMR locus has been linked to DXS8067, DXS1001, DXS425, DXS7877, and DXS1183 with a maximum LOD score of 2.4. The haplotype studies and multipoint linkage analysis suggest a localization of the MRX82 locus to an interval of 7.6 Mb defined by markers DXS6805 and DXS7346, in Xq24 and Xq25, respectively. No gene contained in this interval has been so far associated with nonsyndromic mental retardation, except for GRIA3, disrupted by a balanced translocation in a female patient with bipolar affect…

GeneticsHaplotypeLocus (genetics)Biologymedicine.diseaseDevelopmental disorderGenetic linkageIntellectual disabilityGeneticsmedicinebiology.proteinMicrosatelliteGRIA3Genetics (clinical)X chromosomeAmerican Journal of Medical Genetics Part A
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Validation and casework testing of the BioPlex-11 for STR typing of telogen hair roots.

2005

A new STR typing strategy has been developed allowing the simultaneous amplification and subsequent analysis of 11 polymorphic systems with amplicon sizes smaller than 270 bp. The multiplex amplification reaction includes six STR loci from the European standard set of loci (ESS) for DNA databases (D3S1358, D8S1179, D21S11, THO1, FGA and VWA) as well as four additional STR systems selected for their robustness (D2S1338, D12S391, TPOX and D5S818) together with the sex-specific locus amelogenin. After PCR amplification, the multiplex reaction is splitted into two sets of STR multiplexes by using biotin labelled primers only for one set. Using streptavidin-coated Sepharose beads five STR system…

GeneticsHeterozygoteAmelogeninSTR multiplex systemElectrophoresis CapillaryLocus (genetics)BiologyAmpliconDNA FingerprintingPolymerase Chain ReactionPathology and Forensic Medicinelaw.inventionDental Enamel ProteinslawTandem Repeat SequencesMicrosatelliteHumansMultiplexTypingAmelogeninLawHair FolliclePolymerase chain reactionForensic science international
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Signature of recent historical events in the European Y-chromosomal STR haplotype distribution

2005

Previous studies of human Y-chromosomal single-nucleotide polymorphisms (Y-SNPs) established a link between the extant Y-SNP haplogroup distribution and the prehistoric demography of Europe. By contrast, our analysis of seven rapidly evolving Y-chromosomal short tandem repeat loci (Y-STRs) in over 12,700 samples from 91 different locations in Europe reveals a signature of more recent historic events, not previously detected by other genetic markers. Cluster analysis based upon molecular variance yields two clearly identifiable sub-clusters of Western and Eastern European Y-STR haplotypes, and a diverse transition zone in central Europe, where haplotype spectra change more rapidly with longi…

GeneticsHistoryChromosomes Human YGenotypeDemographic historyHaplotypeContrast (statistics)BiologyPolymorphism Single NucleotideHaplogroupy DNA typingEastern europeanEuropePrehistoric demographyHaplotypesGenetic markerEvolutionary biologyTandem Repeat SequencesGeneticsMicrosatelliteHumansGenetics (clinical)
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Report of the European DNA profiling group (EDNAP)-an investigation of the hypervariable STR loci ACTBP2, APOAI1 and D11S554 and the compound loci D1…

1999

This paper describes the results of three collaborative exercises which continues the EDNAP theme to explore whether uniformity of DNA profiling results could be achieved between European laboratories using STRs. In an earlier exercise, complex hypervariable AAAG-repeat STR loci were investigated, but reproducibility was found to be poor because of the variation of techniques used by participating laboratories. In the exercise reported here, an internal allelic ladder composed of ACTBP2 and D11S554 fragments was distributed. This ladder was used to size ACTBP2 analysed by a "singleplex" PCR amplification and D11S554 combined with APOAI1 in a separate "duplex" reaction. Laboratories were ask…

GeneticsInternational CooperationBlood StainsImmunoglobulin Variable RegionReproducibility of ResultsMinisatellite RepeatsDNA SatelliteBiologyDNA FingerprintingPolymerase Chain ReactionPathology and Forensic Medicinelaw.inventionEuropeDNA profilingMulticenter studylawGenetic markerStr lociHumansMicrosatelliteLawAllelesSocieties MedicalPolymerase chain reactionForensic Science International
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Considerations from the European DNA profiling group (EDNAP) concerning STR nomenclature

1997

(1) The nomenclature of any STR follows from comparison with a control allelic ladder; availability of reference allelic ladders is central to any scheme. The components of an allelic ladder should be sequenced. (2) The DNA commission recommended a nomenclature based upon the number of repeat sequences present in an allele. Whereas this method is suitable for typing simple STRs, complex hypervariable repeats such as ACTBP2 do not conform to a simple repeating structure. We propose that designation of complex STR repeats such as ACTBP2, D11S554 and APOAI1 follows from the size of specific alleles. Because the size is dependant upon the primers utilised, the size is not definitive (it may als…

GeneticsLocus (genetics)DNASequence Analysis DNAForensic MedicineBiologyActinsPathology and Forensic MedicineEuropeType (biology)DNA profilingGenetic markerPolymorphism (computer science)Terminology as TopicHumansMicrosatelliteTypingAlleleLawSocieties MedicalRepetitive Sequences Nucleic AcidForensic Science International
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