Search results for "Animal Genetics"

showing 10 items of 60 documents

Genome-wide scan for selection signatures reveals novel insights into the adaptive capacity in local North African cattle

2020

International audience; Natural-driven selection is supposed to have left detectable signatures on the genome of North African cattle which are often characterized by the fixation of genetic variants associated with traits under selection pressure and/or an outstanding genetic differentiation with other populations at particular loci. Here, we investigate the population genetic structure and we provide a first outline of potential selection signatures in North African cattle using single nucleotide polymorphism genotyping data. After comparing our data to African, European and indicine cattle populations, we identified 36 genomic regions using three extended haplotype homozygosity statistic…

GenotypeEvolutionMolecular biologyQuantitative Trait Locilcsh:MedicineBreedingNorth African cattle selection signatures candidate genePolymorphism Single NucleotideArticleSettore AGR/17 - Zootecnica Generale E Miglioramento GeneticoAfrica NorthernGene FrequencyGeneticsAnimalsSelection Geneticlcsh:ScienceWhole Genome Sequencinglcsh:RGenomicsAdaptation Physiological[SDV.GEN.GA]Life Sciences [q-bio]/Genetics/Animal geneticsGenetics PopulationPhenotypeHaplotypeslcsh:QCattleGenome-Wide Association Study
researchProduct

Conservatism and novelty in the genetic architecture of adaptation in Heliconius butterflies.

2015

Understanding the genetic architecture of adaptive traits has been at the centre of modern evolutionary biology since Fisher; however, evaluating how the genetic architecture of ecologically important traits influences their diversification has been hampered by the scarcity of empirical data. Now, high-throughput genomics facilitates the detailed exploration of variation in the genome-to-phenotype map among closely related taxa. Here, we investigate the evolution of wing pattern diversity in Heliconius, a clade of neotropical butterflies that have undergone an adaptive radiation for wing-pattern mimicry and are influenced by distinct selection regimes. Using crosses between natural wing-pat…

GenotypeQuantitative Trait LociChromosome MappingColor[ SDV.GEN.GA ] Life Sciences [q-bio]/Genetics/Animal geneticsAdaptation PhysiologicalBiological Evolution[SDV.GEN.GA]Life Sciences [q-bio]/Genetics/Animal geneticsPhenotypeAnimalsWings AnimalOriginal ArticleButterfliesCrosses Genetic
researchProduct

Phylogeography and genetic variation of Triatoma dimidiata, the main Chagas disease vector in Central America, and its position within the genus Tria…

2008

Background Among Chagas disease triatomine vectors, the largest genus, Triatoma, includes species of high public health interest. Triatoma dimidiata, the main vector throughout Central America and up to Ecuador, presents extensive phenotypic, genotypic, and behavioral diversity in sylvatic, peridomestic and domestic habitats, and non-domiciliated populations acting as reinfestation sources. DNA sequence analyses, phylogenetic reconstruction methods, and genetic variation approaches are combined to investigate the haplotype profiling, genetic polymorphism, phylogeography, and evolutionary trends of T. dimidiata and its closest relatives within Triatoma. This is the largest interpopulational …

Infectious Diseases/Epidemiology and Control of Infectious Diseaseslcsh:Arctic medicine. Tropical medicinelcsh:RC955-962Molecular Sequence DataZoologyPopulation geneticsMolecular Biology/Molecular EvolutionSubspeciesBiologyDNA RibosomalEvolutionary Biology/Animal GeneticsAdaptive radiationGenetics and Genomics/Population Geneticsparasitic diseasesAnimalsChagas DiseaseTriatoma dimidiataTriatomaCladePhylogenyEvolutionary Biology/Evolutionary and Comparative GeneticsEcologylcsh:Public aspects of medicinePublic Health Environmental and Occupational HealthInfectious Diseases/Protozoal InfectionsGenetic VariationCentral Americalcsh:RA1-1270biology.organism_classificationInsect VectorsPhylogeographyInfectious DiseasesInfectious Diseases/Neglected Tropical DiseasesHaplotypesVector (epidemiology)TriatomaResearch Article
researchProduct

Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene

2015

International audience; Here we describe a spontaneous mutation in the Zdhhc13 (zinc finger, DHHC domain containing 13) gene (also called Hip14l), one of 24 genes encoding palmitoyl acyltransferase (PAT) enzymes in the mouse. This mutation (Zdhhc13luc) was identified as a nonsense base substitution, which results in a premature stop codon that generates a truncated form of the ZDHHC13 protein, representing a potential loss-of-function allele. Homozygous Zdhhc13luc/Zdhhc13luc mice developed generalized hypotrichosis, associated with abnormal hair cycle, epidermal and sebaceous gland hyperplasia, hyperkeratosis, and increased epidermal thickness. Increased keratinocyte proliferation and accel…

KeratinocytesPathologySkin NeoplasmsMutantMESH: Codon TerminatorMESH: Epidermal Cellsmedicine.disease_causeBiochemistryMESH: Acyltransferases / genetics*MESH: Keratinocytes / physiologyMice0302 clinical medicineHair cycleMESH: AnimalsPalmitoyl acyltransferase0303 health sciencesintegumentary systemNF-kappa B3. Good healthPhenotypemedicine.anatomical_structureNeutrophil Infiltration030220 oncology & carcinogenesisCodon TerminatorKeratinocytemedicine.medical_specialtyClinical SciencesOncology and CarcinogenesisDermatologyBiologyMESH: PhenotypeMESH: Skin Neoplasms / etiologyArticleMESH: Skin Neoplasms / genetics*03 medical and health sciencesMESH: Genetic Predisposition to Disease*medicineAnimalsGenetic Predisposition to DiseaseTerminatorMESH: NF-kappa B / physiologyCodonMESH: MiceMolecular Biology030304 developmental biologyEpidermis (botany)Dermatology & Venereal DiseasesMESH: Leukocyte Elastase / metabolismCell BiologyMESH: Bromodeoxyuridine / metabolismNFKB1Molecular biologyMESH: Neutrophil Infiltration[SDV.GEN.GA]Life Sciences [q-bio]/Genetics/Animal geneticsBromodeoxyuridineEpidermal CellsMutationNIH 3T3 CellsMESH: Mutation*Leukocyte ElastaseCarcinogenesisDHHC domainAcyltransferasesMESH: NIH 3T3 CellsJournal of Investigative Dermatology
researchProduct

Effect of sperm concentration and storage temperature on goat spermatozoa during liquid storage

2020

The use of cooled semen is relatively common in goats. There are a number of advantages of cooled semen doses, including easier handling of artificial insemination (AI) doses, transport, more AI doses per ejaculate, and higher fertility rates in comparison with frozen AI doses. However, cooled semen has a short shelf life. The objective of this study was to examine the effect of temperature and sperm concentration on the in vitro sperm quality during liquid storage for 48 h, including sperm motility and kinetics, response to oxidation, mitochondrial membrane potential (MMP) and DNA fragmentation in goats. Three experiments were performed. In the first, the effects of liquid preservation of …

L53 Animal physiology - Reproductionmedicine.medical_treatmentDNA fragmentationmitochondrial activitylaw.invention0302 clinical medicineL10 Animal genetics and breedinglawlcsh:QH301-705.5Semen qualitySperm motilityreproductive and urinary physiologyLiquid Storageliquid storage030219 obstetrics & reproductive medicineMurciano-GranadinaExtenderSperm washingMotilityMitochondrial Activity04 agricultural and veterinary sciencesBiología y Biomedicina / BiologíamotilityDNA fragmentationGeneral Agricultural and Biological SciencesGenetic improvementendocrine systemMotilityShelf lifeSemen ExtendersSemenDNA FragmentationBiologyGeneral Biochemistry Genetics and Molecular BiologyAi (artificial insemination)ArticleAndrology03 medical and health sciencesSemenmedicineU10 Mathematical and statistical methodsgoat spermGeneral Immunology and Microbiologyurogenital systemArtificial insemination0402 animal and dairy scienceGoat Sperm040201 dairy & animal scienceSpermFrozen storagelcsh:Biology (General)
researchProduct

Intra- and intergenotypic larval competition in Drosophila melanogaster : effect of larval density and biotic residues

1987

Larvalcsh:QH426-470biologyResearchmedia_common.quotation_subjectZoology[SDV.GEN.GA] Life Sciences [q-bio]/Genetics/Animal geneticsGeneral Medicinebiology.organism_classificationPopulation densityCompetition (biology)Full articlelcsh:GeneticsEvolutionary biologyDrosophilidaeGeneticsGenetics(clinical)Animal Science and Zoologylcsh:Animal cultureDrosophila melanogasterComputingMilieux_MISCELLANEOUSEcology Evolution Behavior and Systematicslcsh:SF1-1100media_commonGenetics Selection Evolution
researchProduct

Rats bred for low aerobic capacity become promptly fatigued and have slow metabolic recovery after stimulated, maximal muscle contractions.

2012

AIM. Muscular fatigue is a complex phenomenon affected by muscle fiber type and several metabolic and ionic changes within myocytes. Mitochondria are the main determinants of muscle oxidative capacity which is also one determinant of muscle fatigability. By measuring the concentrations of intracellular stores of high-energy phosphates it is possible to estimate the energy production efficiency and metabolic recovery of the muscle. Low intrinsic aerobic capacity is known to be associated with reduced mitochondrial function. Whether low intrinsic aerobic capacity also results in slower metabolic recovery of skeletal muscle is not known. Here we studied the influence of intrinsic aerobic capac…

Magnetic Resonance SpectroscopyAnatomy and PhysiologyPhosphocreatineEvolutionary Selectionlcsh:MedicineIsometric exerciseBreedingmetaboliset sairaudetBiochemistrychemistry.chemical_compound0302 clinical medicineTriceps surae muscleMyocyteta315lcsh:ScienceMusculoskeletal System0303 health sciencesMultidisciplinarycomplex diseaseMuscle BiochemistryAnatomyAnimal ModelsHydrogen-Ion Concentrationmedicine.anatomical_structureaerobinen kapasiteettiMuscle FatigueMuscleaerobinen suorituskykymedicine.symptomMuscle contractionMuscle ContractionResearch Articlemedicine.medical_specialtyEvolutionary ProcessessupistusominaisuudetBioenergeticsPhosphocreatinePhosphates03 medical and health sciencesModel OrganismsInternal medicinePhysical Conditioning AnimalmedicineGeneticsAnimalsskeletal muscleAdaptationBiologyAerobic capacity030304 developmental biologyEvolutionary BiologyMuscle fatiguelcsh:RSkeletal muscleElectric StimulationRatsraajalihasEndocrinologyMetabolismcontractile propertieschemistryRatlcsh:QEnergy MetabolismPhysiological ProcessesAnimal Genetics030217 neurology & neurosurgeryPLoS ONE
researchProduct

Successive Invasion-Mediated Interspecific Hybridizations and Population Structure in the Endangered Cichlid Oreochromis mossambicus.

2013

Hybridization between invasive and native species accounts among the major and pernicious threats to biodiversity. The Mozambique tilapia Oreochromis mossambicus, a widely used freshwater aquaculture species, is especially imperiled by this phenomenon since it is recognized by the IUCN as an endangered taxon due to genetic admixture with O. niloticus an invasive congeneric species. The Lower Limpopo and the intermittent Changane River (Mozambique) drain large wetlands of potentially great importance for conservation of O. mossambicus, but their populations have remained unstudied until today. Therefore we aimed (1) to estimate the autochthonous diversity and population structure among genet…

Male0106 biological sciencesConservation geneticsintraspecific hybridization[SDV.BA] Life Sciences [q-bio]/Animal biologyIntrogression[SDV]Life Sciences [q-bio]Endangered speciesBiodiversityLimnetic Ecologylcsh:MedicinePopulation geneticsIntroduced speciesAquaculture01 natural sciencesstructure de la populationIUCN Red Listhttp://aims.fao.org/aos/agrovoc/c_35412Amplified Fragment Length Polymorphism Analysislcsh:ScienceMozambiquePhylogenyComputingMilieux_MISCELLANEOUShybridation intraspécifiqueAnimal ManagementConservation ScienceFreshwater Ecology0303 health sciencesMultidisciplinaryEcologybiologyEcology[SDV.BA]Life Sciences [q-bio]/Animal biologyAgricultureBiodiversityGene Pool[SDV] Life Sciences [q-bio][ SDV.GEN.GPO ] Life Sciences [q-bio]/Genetics/Populations and Evolution [q-bio.PE]FemaleFish FarmingTilapiaResearch ArticleGene FlowOreochromis mossambicusEvolutionary Processesoreochromis mossambicusGenotypeMolecular Sequence DataAgro-Population EcologyGenetic admixture[SDV.BID]Life Sciences [q-bio]/BiodiversityDNA Mitochondrial010603 evolutionary biology03 medical and health sciencesRiversSpecies SpecificityGeneticsAnimalsespèce invasive14. Life underwaterAdaptationBiologyHybridizationSpecies Extinction030304 developmental biology[ SDV.BID ] Life Sciences [q-bio]/BiodiversityEvolutionary Biology[ SDE.BE ] Environmental Sciences/Biodiversity and Ecology[SDV.GEN.GPO]Life Sciences [q-bio]/Genetics/Populations and Evolution [q-bio.PE]Endangered Specieslcsh:RGenetic VariationBayes Theorempopulation structureSequence Analysis DNA15. Life on landL10 - Génétique et amélioration des animauxbiology.organism_classificationGenetics PopulationHaplotypesGenetic PolymorphismHybridization Geneticlcsh:QM12 - Production de l'aquaculturehttp://aims.fao.org/aos/agrovoc/c_4964[SDE.BE]Environmental Sciences/Biodiversity and EcologyIntroduced SpeciesAnimal GeneticsAgroecologyPopulation Genetics
researchProduct

Causal Link between n-3 Polyunsaturated Fatty Acid Deficiency and Motivation Deficits

2020

International audience; Reward-processing impairment is a common symptomatic dimension of several psychiatric disorders. However, whether the underlying pathological mechanisms are common is unknown. Herein, we asked if the decrease in the n-3 polyunsaturated fatty acid (PUFA) lipid species, consistently described in these pathologies, could underlie reward-processing deficits. We show that reduced n-3 PUFA biostatus in mice leads to selective motivational impairments. Electrophysiological recordings revealed increased collateral inhibition of dopamine D2 receptor-expressing medium spiny neurons (D2-MSNs) onto dopamine D1 receptor-expressing MSNs in the nucleus accumbens, a main brain regio…

Male0301 basic medicineN-3 PUFAPhysiology[SDV]Life Sciences [q-bio]DopamineMice TransgenicNucleus accumbensMedium spiny neuronMice03 medical and health sciences0302 clinical medicineDopamineDopamine receptor D2Fatty Acids Omega-3medicineAnimalsMolecular BiologyPathological030304 developmental biologyNeuronsMedium spiny neuronschemistry.chemical_classification[SDV.GEN]Life Sciences [q-bio]/Genetics0303 health sciencesMotivationReceptors Dopamine D2business.industry[SCCO.NEUR]Cognitive science/NeuroscienceCell BiologyMice Inbred C57BLElectrophysiology[SDV.GEN.GA]Life Sciences [q-bio]/Genetics/Animal geneticsElectrophysiology030104 developmental biologychemistryNucleus accumbensFemalePolyunsaturated fatty acids[SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]Causal linkbusinessNeuroscience030217 neurology & neurosurgerymedicine.drugPolyunsaturated fatty acidCell Metabolism
researchProduct

Aspartoacylase-lacZ knockin mice: an engineered model of Canavan disease.

2011

Canavan Disease (CD) is a recessive leukodystrophy caused by loss of function mutations in the gene encoding aspartoacylase (ASPA), an oligodendrocyte-enriched enzyme that hydrolyses N-acetylaspartate (NAA) to acetate and aspartate. The neurological phenotypes of different rodent models of CD vary considerably. Here we report on a novel targeted aspa mouse mutant expressing the bacterial β-Galactosidase (lacZ) gene under the control of the aspa regulatory elements. X-Gal staining in known ASPA expression domains confirms the integrity of the modified locus in heterozygous aspa lacZ-knockin (aspa(lacZ/+)) mice. In addition, abundant ASPA expression was detected in Schwann cells. Homozygous (…

MaleCentral Nervous SystemCerebellumPathologyAnatomy and PhysiologyCanavan DiseaseMouseMutantlcsh:MedicineNeural HomeostasisBiochemistryMiceNeurobiology of Disease and Regenerationlcsh:ScienceSex CharacteristicsMultidisciplinaryNeuromodulationNeurochemistryGenomicsAnimal ModelsFunctional Genomicsmedicine.anatomical_structureLac OperonNeurologyHomeostatic MechanismsMedicineFemaleNeurochemicalsGenetic EngineeringResearch ArticleNervous System PhysiologyBiotechnologymedicine.medical_specialtyTransgeneCentral nervous systemNeurophysiologyMice TransgenicNeuroimagingBiologyNeurological SystemAmidohydrolasesWhite matterModel OrganismsGeneticsmedicineAnimalsBiologyNeuropeptidesLeukodystrophylcsh:RComputational Biologymedicine.diseaseMolecular biologyCanavan diseaseAspartoacylaseDisease Models AnimalMetabolismnervous systemSmall MoleculesCellular NeuroscienceMetabolic DisordersMutationGenetics of DiseaseNervous System Componentslcsh:QGene FunctionMolecular NeuroscienceAnimal GeneticsNeurosciencePLoS ONE
researchProduct