Search results for "genomics"

showing 10 items of 1255 documents

Ab initio determination of the electron affinities of DNA and RNA nucleobases

2008

High-level quantum-chemical ab initio coupled-cluster and multiconfigurational perturbation methods have been used to compute the vertical and adiabatic electron affinities of the five canonical DNA and RNA nucleobases: uracil, thymine, cytosine, adenine, and guanine. The present results aim for the accurate determination of the intrinsic electron acceptor properties of the isolated nucleic acid bases as described by their electron affinities, establishing an overall set of theoretical reference values at a level not reported before and helping to rule out less reliable theoretical and experimental data and to calibrate theoretical strategies. Daniel.Roca@uv.es Manuela.Merchan@uv.es Luis.Se…

GuanineAb initioGeneral Physics and AstronomyElectronsAb initio calculations ; Coupled cluster calculations ; DNA ; Electron affinity ; Macromolecules ; Molecular biophysics ; Perturbation theoryPerturbation theoryNucleobasechemistry.chemical_compoundCoupled cluster calculationsComputational chemistryAb initio quantum chemistry methodsComputer SimulationPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]Physics::Biological PhysicsQuantitative Biology::BiomoleculesChemistryUracilDNAMolecular biophysicsQuantitative Biology::GenomicsUNESCO::FÍSICA::Química físicaThymineElectron affinityModels ChemicalMacromoleculesNucleic Acid ConformationQuantum TheoryRNAAb initio calculationsCytosineDNAThe Journal of Chemical Physics
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High-throughput sequencing of the 16S rRNA gene to analyze the gut microbiome in juvenile and adult tropical gar (Atractosteus tropicus)

2020

Tropical gar (Atractosteus tropicus) is freshwater and estuarine fish, inhabiting the Earth since the Mesozoic era and undergoing limited physiological variation ever since. Besides its recognized cultural and scientific relevance, the species has seen remarkable growth in its economic impact due to pisciculture. In this study, we present the first report of the whole taxonomic composition of microbial communities in gut contents in juveniles and adults of A. tropicus, by sex and origin (wild and cultivated). For this study, 508 genera were identified, with the most and least abundant being Cetobacterium and Paludibacter, respectively. Fusobacteria, Proteobacteria, Firmicutes, and Bacteroid…

Gut microbiomemetagenomicsFirmicutesPhylumZoologyBacteroidetesAtractosteus tropicusgut microbiomeFusobacteriaAquatic ScienceBiologyGut floraOceanographybiology.organism_classification16S rRNA profilingJuvenilebacteriaMetagenomicsProteobacteriaAtractosteus tropicus
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Endosymbiont communities in Bemisia tabaci: a metagenomic approach

2014

Este trabajo es parte de un programa de investigación que tiene como objetivo dilucidar la evolución de las bacterias endosimbiontes utilizando los consorcios insecto-bacteria como modelo. Los diferentes estudios realizados sobre los insectos y sus bacterias endosimbiontes han arrojado luz sobre los cambios ocurridos tras la adquisición de una forma de vida intracelular, así cómo la interacción entre diferentes endosimbiontes formando comunidades endosimbioticas. Dos son los objetivos principales de este trabajo. El primera (capítulos “Portiera y su socio Hamiltonella” y “El tercer pasajero: Cardinium cBtQ1)” trata de analizar y describir las relaciones de la comunidad endosimbiótica en B. …

Hamiltonella defensa:CIENCIAS DE LA VIDA::Simbiosis [UNESCO]endosymbiosismolecular evolutiongenome stasisUNESCO::CIENCIAS DE LA VIDA::Simbiosisdivergence timecomparative genomicsCardinium hertigii:CIENCIAS DE LA VIDA::Microbiología ::Metabolismo bacteriano [UNESCO]Portiera aleyrodidarumwhitefliesPortiera ultraestructureUNESCO::CIENCIAS DE LA VIDA::Microbiología ::Metabolismo bacterianogliding motilitygenome reductioninsect symbiosismetabolism
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Two Host Clades, Two Bacterial Arsenals: Evolution through Gene Losses in Facultative Endosymbionts.

2015

International audience; Bacterial endosymbiosis is an important evolutionary process in insects, which can harbor both obligate and facultative symbionts. The evolution of these symbionts is driven by evolutionary convergence, and they exhibit among the tiniest genomes in prokaryotes. The large host spectrum of facultative symbionts and the high diversity of strategies they use to infect new hosts probably impact the evolution of their genome and explain why they undergo less severe genomic erosion than obligate symbionts. Candidatus Hamiltonella defensa is suitable for the investigation of the genomic evolution of facultative symbionts because the bacteria are engaged in specific relations…

Hamiltonella defensaVirulence Factors[SDV]Life Sciences [q-bio]fungifood and beveragesGenomicscomparative genomicsbiochemical phenomena metabolism and nutritionBemisia tabaciEvolution MolecularHemipteraaphidsEnterobacteriaceaeCell WallAnimals[INFO.INFO-BI]Computer Science [cs]/Bioinformatics [q-bio.QM]SymbiosisGene DeletionGenome BacterialPhylogenyResearch Article
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Genomics and Proteomics Analyses Revealed Novel Candidate Pesticidal Proteins in a Lepidopteran-Toxic Bacillus thuringiensis Strain

2020

Discovery and identification of novel insecticidal proteins in Bacillus thuringiensis (Bt) strains are of crucial importance for efficient biological control of pests and better management of insect resistance. In this study, the Bt strain KhF, toxic for Plodia interpunctella and Grapholita molesta larvae, underwent genomics and proteomics analyses to achieve a better understanding of the bases of its pathogenicity. The whole-genome sequencing results revealed that the KhF strain contained nine coding sequences with homologies to Bt insecticidal genes. The lepidopteran toxic mixture of spores and crystals of this Bt strain was subjected to liquid chromatography and tandem mass spectrometry …

Health Toxicology and MutagenesisXpp proteinslcsh:MedicineMpp proteinsGenomicsinsect bioassayToxicologymedicine.disease_causeProteomicsTandem mass spectrometryDNA sequencing03 medical and health sciencesBacillus thuringiensismedicinecharacterizationLC-MS/MSGene<i>Plodia interpunctella</i>030304 developmental biology0303 health sciencesStrain (chemistry)biology030306 microbiologyToxinPharmacology. Therapylcsh:Rfungibiology.organism_classificationgenome sequencingBiochemistry<i>Grapholita molesta</i>Toxins
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949 IDENTIFICATION OF TWO CLINICALLY DISTINCT SUBTYPES IN AUTOIMMUNE HEPATITIS BY COMPARATIVE FUNCTIONAL GENOMICS

2013

Conclusion: Incidence of autoimmune hepatitis is increasing, as other autoimmune diseases in developed countries. The main recognised hypothesis is the ‘hygienist theory’ (improvement of hygien leading to a decrease in infections) with few putative non exclusive mechanisms involving antigenic competition, extension of immune regulation induced by exogenous bacterial antigen or Toll Like Receptors.

HepatologyAntigenImmunologyImmune regulationmedicineIdentification (biology)Autoimmune hepatitisBacterial antigenBiologyReceptorBioinformaticsmedicine.diseaseFunctional genomicsJournal of Hepatology
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Screening of hereditary spastic paraplegia patients for alterations at NIPA1 mutational hotspots.

2008

Item does not contain fulltext Mutations in NIPA1 cause hereditary spastic paraplegia type 6 (SPG6 HSP). Sequencing of the whole gene has revealed alterations of either of two nucleotides in eight of nine SPG6 HSP families reported to date. By analysing CpG methylation, we provide a mechanistic explanation for a mutational hotspot to underlie frequent alteration of one of these nucleotides. We also developed PCR RFLP assays to detect recurrent NIPA1 changes and screened 101 independent HSP patients, including 45 index patients of autosomal dominant HSP families. Our negative finding in this cohort for which several other causes of HSP had been excluded suggests NIPA1 alterations at mutation…

Hereditary spastic paraplegiaDNA Mutational AnalysisMolecular Sequence DataCohort StudiesDegenerative diseaseCognitive neurosciences [UMCN 3.2]Polymorphism (computer science)DNA Mutational AnalysismedicineHumansGenetic TestingGeneGeneticsbusiness.industrySpastic Paraplegia HereditaryMembrane ProteinsMethylationDNA Methylationmedicine.diseaseNeurologyDNA methylationNeurology (clinical)Restriction fragment length polymorphismbusinessFunctional Neurogenomics [DCN 2]Polymorphism Restriction Fragment LengthJournal of the Neurological Sciences
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Ancient Haplotypes at the 15q24.2 Microdeletion Region Are Linked to Brain Expression of MAN2C1 and Children's Intelligence

2016

The chromosome bands 15q24.1-15q24.3 contain a complex region with numerous segmental duplications that predispose to regional microduplications and microdeletions, both of which have been linked to intellectual disability, speech delay and autistic features. The region may also harbour common inversion polymorphisms whose functional and phenotypic manifestations are unknown. Using single nucleotide polymorphism (SNP) data, we detected four large contiguous haplotype-genotypes at 15q24 with Mendelian inheritance in 2,562 trios, African origin, high population stratification and reduced recombination rates. Although the haplotype-genotypes have been most likely generated by decreased or abse…

HeredityAutism Spectrum DisorderIntelligenceSocial SciencesChromosome DisordersMAN2C1 geneFamiliesMicePsychologylcsh:ScienceChildChildrenIn Situ HybridizationCognitive ImpairmentIntelligence Testseducation.field_of_studyIntelligence quotientBrainGenomicsNeurologyChromosome DeletionHumanGenotypeEvolutionSingle-nucleotide polymorphismFluorescenceEvolution Molecular03 medical and health sciencesalpha-MannosidaseIntellectual DisabilityMannosidasesGeneticsChromosome 15q24 2HumansPolymorphismeducationChromosome Aberrationslcsh:RHaplotypePair 15PongoBiology and Life SciencesComputational BiologyMolecularmedicine.diseaseIntellectual Disability/genetics030104 developmental biologyNeurodevelopmental DisordersDevelopmental PsychologyAfricalcsh:QPopulation GroupingsGene expressionEthiopiaAutismePopulation GeneticsNeuroscience0301 basic medicineAutismlcsh:MedicineGene ExpressionHomozygosityGeographical LocationsCohort StudiesChromosome Disorders/geneticsIntellectual disabilityMedicine and Health SciencesIn Situ Hybridization FluorescenceSegmental duplicationMannosidases/geneticsGeneticsMultidisciplinaryGenomeCognitive NeurologyHomozygoteSingle NucleotidePhenotypesymbolsInfantsResearch ArticleCognitive NeurosciencePopulationInfants -- DesenvolupamentBiologyPolymorphism Single NucleotideChromosomessymbols.namesakeDevelopmental NeurosciencemedicineAnimalsBrain/metabolismCromosomes humans -- AnomaliesAlleleChromosomes Human Pair 15Evolutionary BiologyPopulation BiologyGenome HumanChromosome 15qIntelligence/geneticsGenome AnalysisGenomic LibrariesExpressió gènicaMacaca mulattaRatsHaplotypesAge GroupsPeople and PlacesMendelian inheritanceCognitive Science
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Testing for goodness rather than lack of fit of an X–chromosomal SNP to the Hardy-Weinberg model

2019

The problem of checking the genotype distribution obtained for some diallelic marker for compatibility with the Hardy-Weinberg equilibrium (HWE) condition arises also for loci on the X chromosome. The possible genotypes depend on the sex of the individual in this case: for females, the genotype distribution is trinomial, as in the case of an autosomal locus, whereas a binomial proportion is observed for males. Like in genetic association studies with autosomal SNPs, interest is typically in establishing approximate compatibility of the observed genotype frequencies with HWE. This requires to replace traditional methods tailored for detecting lack of fit to the model with an equivalence test…

HeredityNormal DistributionDistance MeasurementTrinomial01 natural sciencesLinkage Disequilibrium010104 statistics & probabilityStatisticsLack-of-fit sum of squaresMathematicsVenous ThrombosisMeasurement0303 health sciencesMultidisciplinaryQRSoftware EngineeringGenomicsHardy–Weinberg principleGenetic MappingPhysical SciencesEngineering and TechnologyMedicineResearch ArticleComputer and Information SciencesScienceGeometryAsymptotic distributionVariant GenotypesPolymorphism Single NucleotideMolecular Genetics03 medical and health sciencesGenome-Wide Association StudiesGeneticsTest statisticHumansComputer Simulation0101 mathematicsMolecular BiologyGenetic Association Studies030304 developmental biologyChromosomes Human XModels StatisticalModels GeneticSoftware ToolsBiology and Life SciencesComputational BiologyHuman GeneticsGenome AnalysisProbability TheoryProbability DistributionGenotype frequencyRadiiSample size determinationSample SizeBinomial proportion confidence intervalMathematicsPLOS ONE
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Glutathione and cellular redox control in epigenetic regulation.

2015

Epigenetics is defined as the mitotically/meiotically heritable changes in gene expression that are not due to changes in the primary DNA sequence. Over recent years, growing evidence has suggested a link between redox metabolism and the control of epigenetic mechanisms. The effect of the redox control, oxidative stress, and glutathione (GSH) on the epigenetic mechanisms occur at different levels affecting DNA methylation, miRNAs expression, and histone post-translational modifications (PTMs). Furthermore, a number of redox PTMs are being described, so enriching the histone code. Pioneer works showed how oxidized GSH inhibits the activity of S-adenosyl methionine synthetase, MAT1A, a key en…

HistoneMethyltransferaseEpigenetic regulation of neurogenesisbiologyBiochemistryPhysiology (medical)Histone methyltransferasebiology.proteinHistone codeEpigeneticsHistone DemethylasesBiochemistryEpigenomicsFree radical biologymedicine
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