Search results for " DNA"

showing 10 items of 2475 documents

Suitability of chloroplast LSU rDNA and its diverse group I introns for species recognition and phylogenetic analyses of lichen-forming Trebouxia alg…

2009

To date, species identification of lichen photobionts has been performed principally on the basis of microscopic examinations and molecular data from nuclear-encoded genes. In plants, the chloroplast genome has been more readily exploited than the nuclear genome for systematic investigations. At the present time, very little information is available about the chloroplast genome of lichen-forming algae. For this reason, we have sequenced a portion of the gene encoding for the chloroplast large sub-unit rRNA (LSU rDNA) as a new molecular marker. Sequencing of the chloroplast LSU rDNAs revealed the existence of an unusual diversity of group I introns (a total of 31) within 15 analyzed Trebouxi…

TrebouxiaNuclear geneBiologyDNA RibosomalGenomeEvolution MolecularSpecies SpecificityChlorophytaPhylogeneticsDNA Ribosomal SpacerGeneticsGroup I catalytic intronGenome ChloroplastMolecular BiologyPhylogenyEcology Evolution Behavior and SystematicsCell NucleusGeneticsLikelihood FunctionsPhylogenetic treeDNA Chloroplastfood and beveragesBayes TheoremSequence Analysis DNARibosomal RNAbiology.organism_classificationIntronsChloroplastMolecular Phylogenetics and Evolution
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Life-history trade-offs in a generalist digenean from cetaceans: the role of host specificity and environmental factors

2015

Background Adults and larvae of generalist parasites are exposed to diverse hosts and local environmental conditions throughout their life cycles, thus local adaptation is expected to occur through phenotypic plasticity and/or natural selection. We investigated how the combined effect of cryptic host specificity and local selective pressures could shape reproductive traits of a putative generalist parasite in the oceanic realm. Methods The LSU rDNA, ITS2 and the mt-COI of individuals of the digenean Pholeter gastrophilus (Kossack, 1910) Odhner, 1914 (Heterophyidae Leiper, 1909) from oceanic striped dolphins, Stenella coeruleoalba Meyen, and coastal bottlenose dolphins, Tursiops truncatus Mo…

TroglotrematidaeZygoteMolecular Sequence DataZoologyTrade-offStenella coeruleoalbaBiologyGeneralist and specialist speciesDNA RibosomalHost SpecificityElectron Transport Complex IVStenellabiology.animalDNA Ribosomal Spacerparasitic diseasesMediterranean SeaAnimalsLocal adaptationPhenotypic plasticityHost (biology)EcologyResearchEgg sizefungiIntermediate hostEnvironmental exposureEnvironmental ExposureSequence Analysis DNADNA HelminthStenellaAdaptation PhysiologicalBottle-Nosed DolphinInfectious DiseasesFecundityRNA Ribosomalembryonic structuresParasitologyhuman activitiesDigeneaParasites & Vectors
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Analysis of the p53 and MDM-2 gene in acute myeloid leukemia

1996

The MDM-2 (murine double minute 2) gene codes for a cellular protein that can bind to the p53 tumor suppressor gene product, thereby functioning as a negative regulator of p53. In order to define the role of the MDM-2 gene in the pathogenesis of human acute myeloid leukemia, the expression and the sequence of the MDM-2 gene were examined in samples of bone marrow and/or peripheral mononuclear cells of 38 patients by using immunostaining, polymerase chain reaction (PCR), single strand conformation polymorphism, and sequencing. Immunohistochemical staining detected a weak accumulation of the MDM-2 protein in AML patients of FAB classification M4 and M5. RT-PCR analysis revealed a heterogeneou…

Tumor suppressor geneGene ExpressionBiologyPolymerase Chain ReactionExonBone MarrowProto-Oncogene ProteinsGene expressionmedicineHumansMissense mutationRNA MessengerGenePolymorphism Single-Stranded ConformationalBase SequenceNuclear ProteinsMyeloid leukemiaProto-Oncogene Proteins c-mdm2Single-strand conformation polymorphismExonsSequence Analysis DNAHematologyGeneral MedicineGenes p53medicine.diseaseImmunohistochemistryMolecular biologyLeukemiaLeukemia MyeloidAcute DiseaseLeukocytes MononuclearCancer researchEuropean Journal of Haematology
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Pythium stipitatumsp. nov. isolated from soil and plant debris taken in France, Tunisia, Turkey, and India

2009

Pythium stipitatum is a slow-growing oomycete and has been isolated from soil samples and plant materials from France, Tunisia, Turkey and India. Its morphological characteristics are reminiscent of those of Pythium ramificatum, discovered in Algeria by the corresponding author. Unfortunately, the Algerian isolate was not deposited in any culture collection and ultimately got lost. Those were the days when molecular description of fungi was not a fashion; hence, no molecular characteristics of the Algerian isolates were deposited to the GenBank. Moreover, its coralloid antheridial branches made it an easy prey to be considered as synonymous to Pythium minus. Because there are no living stra…

TunisiaTurkeyMolecular Sequence DataIndiaPythiumPoaceaeMicrobiologySpecies SpecificityDNA Ribosomal SpacerBotanyGeneticsPythiumInternal transcribed spacerDNA FungalMycological Typing TechniquesMolecular BiologySoil MicrobiologyOomycetebiologyfood and beveragesGenes rRNASequence Analysis DNAPlantsRibosomal RNAbiology.organism_classificationAntheridiumGenBankOosporeTaxonomy (biology)FranceBeta vulgarisFEMS Microbiology Letters
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LaXp180, a mammalian ActA-binding protein, identified with the yeast two-hybrid system, co-localizes with intracellular Listeria monocytogenes

2001

The Listeria monocytogenes surface protein ActA is an important virulence factor required for listerial intracellular movement by inducing actin polymerization. The only host cell protein known that directly interacts with ActA is the phosphoprotein VASP, which binds to the central proline-rich repeat region of ActA. To identify additional ActA-binding proteins, we applied the yeast two-hybrid system to search for mouse proteins that interact with ActA. A mouse cDNA library was screened for ActA-interacting proteins (AIPs) using ActA from strain L. monocytogenes EGD as bait. Three different AIPs were identified, one of which was identical to the human protein LaXp180 (also called CC1). Bind…

Two-hybrid screeningImmunologyMolecular Sequence DataAutophagy-Related ProteinsFluorescent Antibody TechniqueStathminmacromolecular substancesmedicine.disease_causeMicrobiologylaw.inventionCell LineMicefluids and secretionsListeria monocytogenesBacterial ProteinslawVirologyTwo-Hybrid System TechniquesmedicineAnimalsHumansListeriosisAmino Acid SequencebiologyReverse Transcriptase Polymerase Chain ReactionBinding proteintechnology industry and agricultureIntracellular Signaling Peptides and ProteinsMembrane ProteinsProteinsListeria monocytogenesActinsBiochemistryPhosphoproteinembryonic structuresCOS CellsRecombinant DNAbiology.proteinbacteriaSignal transductionCarrier ProteinsIntracellularPlasmids
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A new set of DNA macrochips for the yeast Saccharomyces cerevisiae: features and uses

2004

The yeast Saccharomyces cerevisiae has been widely used for the implementation of DNA chip technologies. For this reason and due to the extensive use of this organism for basic and applied studies, yeast DNA chips are being used by many laboratories for expression or genomic analyses. While membrane arrays (macroarrays) offer several advantages, for many laboratories they are not affordable. Here we report that a cluster of four Spanish molecular-biology yeast laboratories, with relatively small budgets, have developed a complete set of probes for the genome of S. cerevisiae. These have been used to produce a new type of macroarray on a nylon surface. The macroarrays have been evaluated and…

UNESCO::CIENCIAS DE LA VIDA::Microbiología ::Metabolismo bacterianoGene AmplificationmacroarraySaccharomyces cerevisiae; DNA chip; MacroarraySaccharomyces cerevisiaeDNA Fungal:CIENCIAS DE LA VIDA::Microbiología ::Metabolismo bacteriano [UNESCO]DNA chipOligonucleotide Array Sequence Analysis
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Heavy metal ion induction of adhesion molecules and cytokines in human endothelial cells: the role of NF-kappaB, I kappaB-alpha and AP-1.

1997

We analyzed the influence of heavy-metal ions on human umbilical vein endothelial cells (HUVEC) in comparison to proinflammatory cytokines (TNF-alpha, IL-1beta) and lipopolysaccharide (LPS). Adhesion molecule and cytokine expressions are upregulated by heavy-metal exposure. Expression of E-selectin on the cell surface was strongly induced by 1-mM concentrations of NiCl2 and CoCl2, whereas ZnCl2 and CrCl3 had no influence. Furthermore, it is shown that NiCl2 induces mRNA expression of E-selectin, intercellular adhesion molecule-1, IL-6 and IL-8 in a 1-mM concentration. The transcription factor NF-kappaB is known to be involved in the regulation of adhesion molecule expression in endothelial …

Umbilical VeinsLipopolysaccharideBlotting WesternUmbilical veinPathology and Forensic MedicineProinflammatory cytokineMetalchemistry.chemical_compoundNF-KappaB Inhibitor alphaMetals HeavyHumansRNA MessengerMolecular BiologyCells CulturedCell adhesion moleculeChemistrySingle-Strand Specific DNA and RNA EndonucleasesNF-kappa BNF-κBCell BiologyGeneral MedicineAdhesionBlotting NorthernMolecular biologyCell biologyUp-RegulationDNA-Binding ProteinsTranscription Factor AP-1Gene Expression Regulationvisual_artcardiovascular systemvisual_art.visual_art_mediumCytokinesTetradecanoylphorbol AcetateI-kappa B ProteinsEndothelium VascularSignal transductionDNA ProbesCell Adhesion MoleculesPathobiology : journal of immunopathology, molecular and cellular biology
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Conserved alternative splicing in the 5'-untranslated region of the muscle-specific enolase gene. Primary structure of mRNAs, expression and influenc…

1995

We report here the isolation and characterization of cDNAs covering the 5'-end region of mouse and rat mRNAs that encode the beta or muscle-specific isoform of the glycolytic enzyme enolase. As previously determined for humans, two classes of beta-enolase transcripts with distinct sequences in their 5'-untranslated regions are present in both mouse and rat muscles. A mechanism of alternative splicing, conserved from mouse to man, generates the two forms of mRNA. Secondary-structure predictions indicated that, in all cases, a more stable secondary structure could exist in the 5' end of the message with the longer leader. In vitro transcripts containing defined human or mouse 5'-untranslated …

Untranslated regionGene isoformFive prime untranslated regionMolecular Sequence DataBiologyBiochemistryMicePolysomeComplementary DNAAnimalsHumansRNA MessengerMuscle SkeletalGeneConserved SequenceMessenger RNABase SequenceMolecular StructureAlternative splicingMolecular biologyRatsAlternative SplicingPhosphopyruvate HydrataseProtein BiosynthesisRabbitsSequence AlignmentEuropean journal of biochemistry
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A sequence element downstream of the yeast HTB1 gene contributes to mRNA 3' processing and cell cycle regulation.

2002

Histone mRNAs accumulate in the S phase and are rapidly degraded as cells progress into the G(2) phase of the cell cycle. In Saccharomyces cerevisiae, fusion of the 3' untranslated region and downstream sequences of the yeast histone gene HTB1 to a neomycin phosphotransferase open reading frame is sufficient to confer cell cycle regulation on the resulting chimera gene (neo-HTB1). We have identified a sequence element, designated the distal downstream element (DDE), that influences both the 3'-end cleavage site selection and the cell cycle regulation of the neo-HTB1 mRNA. Mutations in the DDE, which is located approximately 110 nucleotides downstream of the HTB1 gene, lead to a delay in the…

Untranslated regionSaccharomyces cerevisiae ProteinsGenes FungalMolecular Sequence DataSaccharomyces cerevisiaeGene ExpressionSaccharomyces cerevisiaeRegulatory Sequences Nucleic AcidPrimary transcriptHistonesOpen Reading FramesGene Expression Regulation FungalMolecular BiologyGeneS phaseBase SequencebiologyCell CycleSingle-Strand Specific DNA and RNA EndonucleasesCell BiologyCell cyclebiology.organism_classificationMolecular biologyDNA-Binding ProteinsHistoneMutagenesis Site-Directedbiology.proteinNucleic Acid ConformationRNA 3' End ProcessingG1 phase
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HSP70 gene expression in Mytilus galloprovincialis hemocytes is triggered by moderate heat shock and Vibrio anguillarum, but not by V. splendidus or …

2005

Complete sequence of HSP70 cDNA from the mussel, Mytilus galloprovincialis was established before quantifying its expression following moderate heat shock or injection of heat-killed bacteria. HSP70 cDNA is comprised of 2378 bp including one ORF of 654 aa, with a predicted 70 bp 5'-UTR and a 343 bp 3'-UTR (GenBank, 18 Jan 05, AY861684). Alignment identity ranged from 89% for Crassostrea ariakensis to 72% for C. virginica. Curiously, HSP70 gene and cDNA sequences from M. galloprovincialis, deposited later (03 and 27 May), show only 73% identity with the present sequence. Meanwhile, characteristic motifs of the HSP70 family were located in conserved positions. Expression of HSP70 gene was qua…

Untranslated regionVibrio anguillarumHemocytesMolecular Sequence DataImmunologyMicrococcusMicrobiologyComplementary DNAGene expressionAnimalsHSP70 Heat-Shock ProteinsAmino Acid SequenceCloning MolecularPhylogenyVibrioMytilusBase SequencebiologyReverse Transcriptase Polymerase Chain Reactionbiology.organism_classificationMytilusRandom Amplified Polymorphic DNA TechniqueHousekeeping geneHsp70RNA28S rRNA Gene expression Heat shock HSP70Sequence AlignmentHeat-Shock ResponseBacteriaDevelopmental BiologyDevelopmental & Comparative Immunology
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