Search results for "Intergenic region"

showing 10 items of 49 documents

AnABlast: Re-searching for Protein-Coding Sequences in Genomic Regions

2019

AnABlast is a computational tool that highlights protein-coding regions within intergenic and intronic DNA sequences which escape detection by standard gene prediction algorithms. DNA sequences with small protein-coding genes or exons, complex intron-containing genes, or degenerated DNA fragments are efficiently targeted by AnABlast. Furthermore, this algorithm is particularly useful in detecting protein-coding sequences with nonsignificant homologs to sequences in databases. AnABlast can be executed online at http://www.bioinfocabd.upo.es/anablast/ .

Fossil DNA sequencesProtein coding0303 health sciencesGene predictionCoding DNA sequences030302 biochemistry & molecular biologyComputational biologyBiologyGene findingDNA sequencing03 medical and health sciencesExonchemistry.chemical_compoundIntergenic regionchemistryHomologous chromosomeSmall genesGeneIn silico annotation toolDNA030304 developmental biology
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New Foldback transposable element TFB1 found in histone genes of the midge Chironomus thummi

1990

A new Foldback transposable element (TFB1) has been found in the histone H1-H3 intergenic region in the midge Chironomus thummi thummi. TFB1 has long terminal inverted repeats, composed of short, degenerate subrepeats and is flanked by nine or ten base-pair “target site” duplications. TFB1 is present in at least two adjacent histone gene units in Ch. th. thummi, indicating a homogenization of histone gene repeats. The copy number and chromosomal distribution of TFB1 are different in the closely related subspecies Ch. th. thummi and Ch. th. piger, showing that amplification, elimination and transposition of TFB1 have occurred recently during evolution.

GeneticsTransposable elementBase SequenceFoldback (sound engineering)Inverted repeatMolecular Sequence DataRestriction MappingGene AmplificationNucleic acid sequenceBiologyBiological EvolutionChironomidaeHistonesTransposition (music)Intergenic regionHistoneStructural BiologyMutationDNA Transposable Elementsbiology.proteinAnimalsMolecular BiologyGeneRepetitive Sequences Nucleic AcidJournal of Molecular Biology
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Polymorphisms in the intergenic region of the sea urchin Paracentrotus lividus ribosomal DNA

1990

Abstract Blot-hybridizations of the sea urchin Paracentrotus lividus genomic DNA with ribosomal DNA (rDNA) probes revealed individual variations in the length and in the sequence of the non-transcribed spacer (NTS) region. The number of rDNA repeat subclasses distinguishable within any individual sea urchin is usually limited (1 to 3) with respect to the widest polymorphism of the population as a whole. The heterogeneity in sequence is revealed by the presence or the absence of specific restriction sites in the spacer region. The data obtained by the intensity of the polymorphic bands indicate that different mechanisms bring about these two types of polymorphism. Preliminary data also indic…

Geneticseducation.field_of_studybiologyPopulationCell Biologybiology.organism_classificationParacentrotus lividusgenomic DNARestriction siteRestriction mapIntergenic regionbiology.animaleducationRibosomal DNASea urchinCell Biology International Reports
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Intraspecific and within-isolate sequence variation in the ITS rRNA gene region of Pythium mercuriale sp. nov. (Pythiaceae)

2008

Belbahri, Lassaad et al.

HeterozygoteNuclear geneGenotypeMolecular Sequence DataPythiumBiologyDNA RibosomalMicrobiologyDNA AlgalPeptide Elongation Factor 1Intergenic regionTubulinPhylogeneticsDNA Ribosomal SpacerGeneticsCluster AnalysisPythiumInternal transcribed spacerMolecular BiologyAllelesPhylogenyGeneticsPolymorphism GeneticPhylogenetic treeAlgal ProteinsGenes rRNASequence Analysis DNARibosomal RNAbiology.organism_classificationPythiaceaePhenotype
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A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.

2007

DYX3, a locus for dyslexia, resides on chromosome 2p11-p15. We have refined its location on 2p12 to a 157 kb region in two rounds of linkage disequilibrium (LD) mapping in a set of Finnish families. The observed association was replicated in an independent set of 251 German families. Two overlapping risk haplotypes spanning 16 kb were identified in both sample sets separately as well as in a joint analysis. In the German sample set, the odds ratio for the most significantly associated haplotype increased with dyslexia severity from 2.2 to 5.2. The risk haplotypes are located in an intergenic region between FLJ13391 and MRPL19/C2ORF3. As no novel genes could be cloned from this region, we hy…

MaleRibosomal ProteinsCandidate geneLinkage disequilibriumHeterozygoteTranscription GeneticLocus (genetics)BiologyPolymorphism Single NucleotideLinkage DisequilibriumDyslexiaEvolution MolecularMitochondrial Proteins03 medical and health sciences0302 clinical medicineIntergenic regionGene mappingDCDC2GermanyGeneticsmedicineAnimalsHumansFamilyMolecular BiologyGenetics (clinical)FinlandPhylogeny030304 developmental biologyGenetics0303 health sciencesHaplotypeDyslexiaBrainChromosome MappingGeneral Medicinemedicine.diseaseRepressor ProteinsPhenotypeHaplotypesChromosomes Human Pair 2Female030217 neurology & neurosurgeryHuman molecular genetics
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Direct sequencing of Legionella pneumophila from respiratory samples for sequence-based typing analysis.

2009

ABSTRACT We have developed a procedure to test the efficiency and reliability of sequencing of Legionella pneumophila genes directly from respiratory samples and have compared the results with those derived from cultured isolates. We tried to obtain the nucleotide sequences of six protein-coding loci included in the sequence-based typing scheme for Legionella pneumophila and three intergenic regions from 132 samples corresponding to 106 patients positive for urine antigen. A seminested PCR approach was used to amplify and sequence these nine loci directly from respiratory samples. Nucleotide sequences were directly obtained for 23 Legionella isolates and also for 66 respiratory secretions f…

Microbiology (medical)DNA BacterialBodily SecretionsGenotypeSequence analysisLegionellaRespiratory SystemLegionella pneumophilaPolymerase Chain ReactionSensitivity and Specificitylaw.inventionMicrobiologyLegionella pneumophilaIntergenic regionBacterial ProteinslawmedicineHumansTypingPolymerase chain reactionbiologyMolecular epidemiologyBacteriologySequence Analysis DNAbiology.organism_classificationmedicine.diseasebacterial infections and mycosesVirologyrespiratory tract diseasesBacterial Typing TechniquesbacteriaLegionnaires' diseaseDNA IntergenicLegionnaires' DiseaseJournal of clinical microbiology
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Comparison of clinical and environmental samples of Legionella pneumophila at the nucleotide sequence level

2009

Legionella pneumophila serogroup 1 is the most common etiological agent of legionellosis. We have used clinical and environmental isolates from different sources to compare their genetic variability. We have obtained the nucleotide sequence for six protein-coding loci, included in the SBT scheme for L. pneumophila, and three intergenic regions from 127 samples, 47 of environmental origin and 80 from clinical samples. Levels of genetic variability were found to be higher in the environmental than in the clinical samples, but these did not represent a mere subset of the former. Not a single case of full identity between clinical and environmental isolates was found, which raises the possibili…

Microbiology (medical)Sequence analysisPopulationBiologyMicrobiologyLegionella pneumophilaLegionella pneumophilaIntergenic regionEnvironmental MicrobiologyGeneticsHumansGenetic variabilityLegionella pneumophila Serogroup 1educationMolecular BiologyPhylogenyEcology Evolution Behavior and SystematicsRecombination GeneticGeneticsAnalysis of VarianceMolecular Epidemiologyeducation.field_of_studyPolymorphism GeneticPhylogenetic treeMolecular epidemiologySequence Analysis DNAbiology.organism_classificationGenetics PopulationInfectious DiseasesLegionnaires' DiseaseInfection, Genetics and Evolution
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Characterization of Shiga toxin-producing Escherichia coli O157:H7 isolated in Italy and in France

2002

ABSTRACT Twenty-one Escherichia coli O157:H7 strains isolated in northern Italy from sporadic cases of hemolytic-uremic syndrome and from cattle and food were characterized by virulence gene analysis, pulsed-field gel electrophoresis (PFGE) of Xba I-digested DNA, enterobacterial repetitive intergenic consensus (ERIC) sequence-based PCR (ERIC-PCR), and antibiotic resistance patterns and compared to 18 strains isolated in France from human cases of diarrhea, cattle, and the environment. Strains isolated in Sicily (southern Italy) from a local farm (one strain) and from calves just imported from France (11 strains) and Spain (six strains) were also typed. Whereas the eae and hlyA genes were al…

Microbiology (medical)Settore MED/07 - Microbiologia E Microbiologia ClinicaMeatEpidemiologyCattle DiseasesVirulenceMicrobial Sensitivity TestsEscherichia coli O157Shiga Toxin 1medicine.disease_causePolymerase Chain ReactionShiga Toxin 2law.inventionMicrobiologychemistry.chemical_compoundIntergenic regionShiga-like toxinlawGenotypePulsed-field gel electrophoresismedicineAnimalsHumansChildEscherichia coliEscherichia coli InfectionsPhylogenyPolymerase chain reactionVirulencebiologyShiga toxinShiga Toxin Escherichia coli O157:H7Anti-Bacterial AgentsBacterial Typing TechniquesElectrophoresis Gel Pulsed-FieldItalychemistryHemolytic-Uremic Syndromebiology.proteinCattleFrance
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Systematics of Mepraia (Hemiptera-Reduviidae): cytogenetic and molecular variation.

2009

The haematophagous insects of the subfamily Triatominae (Hemiptera-Reduviidae) have great epidemiological importance as vectors of Trypanosoma cruzi, the causative agent of Chagas disease. Mepraia was originally described as a monotypic genus comprised of Mepraia spinolai, distributed along coastal areas of northern Chile (from Region I to the Metropolitan Region). Recently, some M. spinolai populations have been ranked as a new species named Mepraia gajardoi. Several populations along the distribution range of the genus were sampled, and genetic differentiation was studied based upon the analysis of three molecular markers: cytogenetics (karyotype and chromosome behaviour during meiosis us…

Microbiology (medical)SystematicsMaleMitochondrial DNAMolecular Sequence DataMicrobiologyPolymerase Chain ReactionMepraiaCytogeneticsIntergenic regionGeneticsAnimalsChagas DiseaseChileGonadsMolecular BiologyRibosomal DNAEcology Evolution Behavior and SystematicsPhylogenyGeneticsPolymorphism GeneticbiologyMolecular epidemiologyBase SequenceGeographyChromosomebiology.organism_classificationInsect VectorsInfectious DiseasesReduviidaeEvolutionary biologyDNA IntergenicFemaleTriatominaeSequence AlignmentInfection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases
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Identifying four Trypanosoma cruzi I isolate haplotypes from different geographic regions in Colombia

2007

Abstract Trypanosoma cruzi has been classified into the groups T. cruzi I and T. cruzi II. The latter is subdivided into five smaller lineages based on multilocus enzyme electrophoresis and random amplified polymorphic DNA, designated as IIa-IIe, which shows correspondence with rRNA/mini-exon lineages. Twelve previously characterised T. cruzi isolates from different hosts, including humans, Didelphis marsupialis, and triatomines were analysed to establish genetic variability in T. cruzi group T. cruzi I isolates from different geographical regions of Colombia. DNA samples were sequenced based on the mini-exon gene intergenic region. Sequences were analysed using Clustal W, Staden 1.5 and ME…

Microbiology (medical)Trypanosoma cruziMolecular Sequence DataSingle-nucleotide polymorphismColombiaBiologyPolymorphism Single NucleotideMicrobiologyIntergenic regionparasitic diseasesGenetic variationGeneticsAnimalsGenetic variabilityTrypanosoma cruziMolecular BiologyEcology Evolution Behavior and SystematicsGeneticsBase SequenceGeographyHaplotypeExonsRibosomal RNAbiology.organism_classificationInfectious DiseasesHaplotypesGenBankMicrosatellite RepeatsInfection, Genetics and Evolution
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