Search results for "Microsatellite"

showing 10 items of 425 documents

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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Results of collaborative study regarding the standardization of the Y-linked STR system DYS385 by the European DNA Profiling (EDNAP) group.

1999

Y-chromosome linked short tandem repeat (STR) loci are inherited as a closely linked haplotype, which appears to remain stable in a given paternal lineage over many generations. In forensic cases, Y-linked STRs are particularly useful for the identification of human remains as well as in rape cases with mixed male/female stain samples. DYS385 is derived from tandemly duplicated segments of the Y chromosome thus giving rise to two fragments of variable length which do not behave like alleles but genotypes. The European DNA Profiling (EDNAP) group has carried out a collaborative exercise among 14 participating laboratories using DYS385 for typing of five unknown bloodstains and a control samp…

GeneticsMaleGenetic LinkageSTR multiplex systemInternational CooperationHaplotypeReproducibility of ResultsMinisatellite RepeatsBiologyY chromosomeBlood Protein ElectrophoresisDNA FingerprintingPathology and Forensic MedicineEuropeGenetics PopulationDNA profilingBlood StainsY ChromosomeGenotypeY linkageMicrosatelliteHumansTypingLawForensic science international
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Potential linkage for schizophrenia on chromosome 22q12-q13: a replication study.

1995

In an attempt to replicate a potential linkage on chromosome 22q12-q13.1 reported by Pulver et al. [1994: Am J Med Genet 54:36–43], we have analyzed 4 microsatellite markers which span this chromosomal region, including the IL2RB locus, for linkage with schizophrenia in 30 families from Israel and Germany. Linkage analysis by pairwise lod score analysis as well as by multipoint analysis did not provide evidence for a single major gene locus. However, a lod score of Zmax = 0.612 was obtained for a dominant model of inheritance with the marker D22S304 at recombination fraction 0.2 by pairwise analysis. In addition, using a non-parametric method, sib pair analysis, a P value of 0.068 correspon…

GeneticsMaleModels GeneticGenetic LinkageChromosomes Human Pair 22Locus (genetics)BiologyMajor genePedigreeGene mappingIL2RBGenetic linkageGermanyChromosomal regionSchizophreniaMicrosatelliteHumansFemaleIsraelGenetics (clinical)Recombination FractionAmerican journal of medical genetics
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No inbreeding depression but increased sexual investment in highly inbred ant colonies.

2012

Inbreeding can lead to the expression of deleterious recessive alleles and to a subsequent fitness reduction. In Hymenoptera, deleterious alleles are purged in haploid males moderating inbreeding costs. However, in these haplodiploid species, inbreeding can result in the production of sterile diploid males. We investigated the effects of inbreeding on the individual and colony level in field colonies of the highly inbred ant Hypoponera opacior. In this species, outbreeding winged sexuals and nest-mating wingless sexuals mate during two separate reproductive periods. We show that regular sib-matings lead to high levels of homozygosity and the occasional production of diploid males, which spo…

GeneticsMalePopulation fragmentationAntsOutbreeding depressionReproductionfungiHomozygoteGenetic purgingZoologyHymenopteraBiologyAnt colonybiology.organism_classificationSexual Behavior AnimalGeneticsHaplodiploidyInbreeding depressionAnimalsBody SizeFemaleInbreedingInbreedingEcology Evolution Behavior and SystematicsMicrosatellite RepeatsMolecular ecology
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Multiple quantitative trait loci influence intra-specific variation in genital morphology between phylogenetically distinct lines of Drosophila monta…

2011

The evolution of animal genitalia has gained renewed interest because of their potential roles during sexual selection and early stages of species formation. Although central to understanding the evolutionary process, knowledge of the genetic basis of natural variation in genital morphology is limited to a very few species. Using an outbred cross between phylogenetically distinct lines of Drosophila montana, we characterized quantitative trait loci (QTLs) affecting the size and shape of the distiphallus, a prominent part of the male intromittent organ. Our microsatellite-based linkage analysis shows that intra-specific variation in the distiphallus involves several QTLs of largely additive …

GeneticsMate choicePleiotropyEvolutionary biologySexual selectionGenetic algorithmGenetic variationTraitfood and beveragesMicrosatelliteQuantitative trait locusBiologyEcology Evolution Behavior and SystematicsJournal of Evolutionary Biology
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