Search results for "HAp"

showing 10 items of 2767 documents

Sequence characterization of the melanocortin 1 receptor (MC1R) gene in sheep with different coat colour and identification of the putative e allele …

2010

Abstract Sequence of the melanocortin 1 receptor (MC1R) gene (the Extension locus) was obtained from a panel of 73 animals belonging to 9 Italian sheep breeds or populations (Appenninica, Bergamasca, Comisana, Cornigliese-like, Delle Langhe, Massese, Merinizzata Italiana, Sarda and Valle del Belice) with different coat colours. Evaluation of the identified polymorphisms on this phenotype was reported with in silico predictions and comparative approaches within and across breeds and across species. Five novel single nucleotide polymorphisms (SNPs), organized in three haplotypes, were detected. Another haplotype, including the two missense mutations already described for the ED allele, was id…

GeneticsHaplotypeCoat colour; MC1R; Missense mutation; Ovine breedsSingle-nucleotide polymorphismLocus (genetics)BiologyOvine breedsSettore AGR/17 - Zootecnica Generale E Miglioramento GeneticoCOAT COLOURFood AnimalsSHEEPBREEDSMC1REpistasisAnimal Science and ZoologyMissense mutationAlleleGeneAllele frequencyPOLYMORPHISMSMelanocortin 1 receptor
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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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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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Interleukin-10 promoter polymorphism in sporadic Alzheimer's disease.

2003

Proinflammatory cytokines and acute-phase proteins play an important role in Alzheimer's disease (AD) neurodegeneration, and common polymorphisms of genes controlling their high production have been shown to be associated with AD. Thus, AD patients display a proinflammatory genotype and the control of inflammation might play a protective role in AD development. By sequence-specific probes, we have evaluated the role of anti-inflammatory cytokine interleukin(IL)-10 in AD, by analysing in 132 AD patients and 213 healthy controls the prevalence of three different haplotypes, involving three single-nucleotide polymorphisms (SNPs) at -1082 (G--A), -819 (C--T) and -592 (C--A) nucleotides of IL-10…

GeneticsInflammationImmunologyHaplotypeInterleukinSingle-nucleotide polymorphismBiologyProinflammatory cytokineInterleukin-10Interleukin 10Alzheimer DiseaseImmunologyGenotypeGeneticsSNPHumansAllelePromoter Regions GeneticGenetics (clinical)Genes and immunity
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Towards a Physical Map of the HLA Complex

1989

The human major histocompatibility (HLA) complex is located on the short arm of chromosome 6 in the 6p21.31→6p21.33 region (1,2). There are three clusters of genes, the HLA class I, II, and III regions. Whereas the class III loci are only moderately polymorphic (see (3) for review), the class I and II genes which encode cell surface glycoproteins show an extreme degree of polymorphism. There are a minimum of 17 class I loci (4) and at least 15 genes for class II alpha and beta chains (5). In addition, we (6) and others (7) have recently demonstrated that also the loci for tumor necrosis factor (TNFA) and lymphotoxin (TNFB) are part of the HLA complex [see also Ragoussis et al., this volume]…

GeneticsLinkage disequilibriumPolymorphism (computer science)HaplotypeChromosomeHuman leukocyte antigenAlleleBiologyGeneHLA Complex
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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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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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The STR252-IVS10nt546-VNTR7 phenylalanine hydroxylase minihaplotype in five Mediterranean samples.

1997

IVS10nt546 (IVS10nt-11g→a) is the most common molecular defect of the phenylalanine hydroxylase gene causing phenylketonuria in Mediterranean populations. Previous studies have proposed various and alternative hypotheses concerning the geographical origin and pattern of diffusion of this mutation in this area. In this study, this issue was re-examined on a large sample (149) of “Mediterranean” IVS10nt546 mutant alleles analysed with multiallelic intragenic polymorphisms. The analysis of intragenic microsatellite (STR) and minisatellite (VNTR) polymorphisms shows allelic heterogeneity of the IVS10nt546 mutation. Eight STR and three VNTR alleles were found in association with the splicing def…

GeneticsMediterranean RegionHaplotypePopulation geneticsPhenylalanine HydroxylaseMinisatellite RepeatsBiologyGene flowMinisatelliteGene FrequencyHaplotypesPhenylketonuriasMutation (genetic algorithm)GeneticsMicrosatelliteHumansPoint MutationAllelic heterogeneityAlleleGenetics (clinical)Microsatellite RepeatsHuman genetics
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Intergenomic interactions affect female reproduction: evidence from introgression and inbreeding depression in a haplodiploid mite

2004

Nuclear and cytoplasmic genomes can coevolve antagonistically or harmoniously to affect fitness. One commonly used test for nuclear-cytoplasmic coadaptation relies on the breakup of coadapted gene complexes by introgression, potentially resulting in an increased frequency of nuclear alleles in deleterious interaction with an alien cytoplasm. We investigated the phenotypic effect of such genes on female reproduction in outbred and inbred introgressed lines of the haplodiploid mite Tetranychus urticae. Introgression changed female lifetime fecundity and increased male production, in ways suggesting a control of fecundity by nuclear genes. Conversely introgression reduced the fertilization rat…

GeneticsMiteseducation.field_of_studyNuclear genePopulationIntrogressionHaploidyBiologyFecundityFertilityGeneticsInbreeding depressionHaplodiploidyAnimalsFemaleInbreedingAlleleeducationInbreedingGenetics (clinical)Heredity
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The genetic structure of Drosophila subobscura populations from the islands of Majorca and Minorca (Balearic Islands, Spain) based on allozymes and m…

1999

The genetic structure of seven populations of Drosophila subobscura from different locations on Majorca and Minorca (Balearic Islands, Spain) was studied using two types of markers: allozyme and mitochondrial DNA restriction analyses. Both markers showed congruent results. In the allozyme data, when the Acph-1 locus was excluded from the joint FST statistics, only three out of 21 comparisons were statistically significant, lending support to the hypothesis of low genetic differentiation. The mtDNA restriction analyses showed two haplotypes at a high frequency (more than 40% each), irrespective of the location considered, and a number of endemic haplotypes at very low frequencies (not higher…

GeneticsMitochondrial DNABalearic islandsHaplotypegovernment.political_districtLocus (genetics)BiologyDNA MitochondrialDrosophila subobscuraEnzymesGenetic differentiationGenetics PopulationGene FrequencyEvolutionary biologyGenetic structureGeneticsgovernmentAnimalsDrosophilaFemaleAllelesPhylogenyGenetics (clinical)Heredity
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