Search results for "ogas"

showing 10 items of 902 documents

Nuclear receptors modulate the interaction of Sp1 and GC-rich DNA via ternary complex formation

2000

Binding sites for transcription factor Sp1have been implicated in the transcriptional regulation of several genes by hormones or vitamins, and here we show that a GC-rich element contributes to the retinoic acid response of the interleukin 1β promoter. To explain such observations, it has been proposed that nuclear receptors can interact with Sp1 bound to GC-rich DNA. However, evidence supporting this model has remained indirect. So far, nuclear receptors have not been detected in a complex with Sp1 and GC-rich DNA, and the expected ternary complexes in non-denaturing gels were not seen. In search for these missing links we found that nuclear receptors [retinoic acid receptor (RAR), thyroid…

Cell ExtractsTranscriptional ActivationReceptors Retinoic AcidSp1 Transcription FactorRecombinant Fusion ProteinsReceptors Cytoplasmic and NuclearTretinoinRetinoic acid receptor betaBiologyRetinoid X receptorLigandsResponse ElementsTransfectionModels BiologicalBiochemistryAntibodiesCell LineSubstrate SpecificityAnimalsPromoter Regions GeneticMolecular BiologyNuclear receptor co-repressor 1Nuclear receptor co-repressor 2Binding SitesReceptors Thyroid HormoneDNACell BiologyRetinoic acid receptor gammaRetinoid X receptor gammaGC Rich SequenceProtein Structure TertiaryNuclear receptor coactivator 1Retinoic acid receptorDrosophila melanogasterEcdysteroneRetinoid X ReceptorsOligodeoxyribonucleotidesBiochemistryReceptors CalcitriolThermodynamicsResearch ArticleInterleukin-1Protein BindingTranscription FactorsBiochemical Journal
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Timing of identity: spatiotemporal regulation of hunchback in neuroblast lineages of Drosophila by Seven-up and Prospero.

2006

Neural stem cells often generate different cell types in a fixed birth order as a result of temporal specification of the progenitors. In Drosophila, the first temporal identity of most neural stem cells(neuroblasts) in the embryonic ventral nerve cord is specified by the transient expression of the transcription factor Hunchback. When reaching the next temporal identity, this expression is switched off in the neuroblasts by seven up (svp) in a mitosis-dependent manner, but is maintained in their progeny (ganglion mother cells). We show that svpmRNA is already expressed in the neuroblasts before this division. After mitosis, Svp protein accumulates in both cells, but the downregulation of h…

Cell typeReceptors Steroidanimal structuresTranscription GeneticMitosisNerve Tissue ProteinsNeuroblastAnimalsDrosophila ProteinsCell LineageProgenitor cellMolecular BiologyMitosisGeneticsNeuronsbiologyStem CellsfungiGene Expression Regulation DevelopmentalNuclear ProteinsProsperobiology.organism_classificationEmbryonic stem cellNeural stem cellCell biologyDNA-Binding ProteinsDrosophila melanogasterGanglion mother cellDevelopmental BiologyTranscription FactorsDevelopment (Cambridge, England)
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The ladybird homeobox genes are essential for the specification of a subpopulation of neural cells

2004

AbstractIn Drosophila, neurons and glial cells are produced by neural precursor cells called neuroblasts (NBs), which can be individually identified. Each NB generates a characteristic cell lineage specified by a precise spatiotemporal control of gene expression within the NB and its progeny. Here we show that the homeobox genes ladybird early and ladybird late are expressed in subsets of cells deriving from neuroblasts NB 5-3 and NB 5-6 and are essential for their correct development. Our analysis revealed that ladybird in Drosophila, like their vertebrate orthologous Lbx1 genes, play an important role in cell fate specification processes. Among those cells that express ladybird are NB 5-6…

Cellular differentiationApoptosisAnimals Genetically ModifiedNeuroblastPrecursor cellGlial cellsmedicineHomeoboxAnimalsDrosophila ProteinsCell LineageMolecular BiologyBody PatterningGeneticsHomeodomain ProteinsNeuronsbiologyGene Expression Regulation DevelopmentalCell DifferentiationCell Biologybiology.organism_classificationLadybirdCell biologymedicine.anatomical_structureDrosophila melanogasternervous systemVentral nerve cordIdentity specificationHomeoboxNeurogliaDrosophilaDrosophila melanogasterCNSNeurogliaDrosophila ProteinTranscription FactorsDevelopmental BiologyDevelopmental Biology
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Cyclin E acts under the control of Hox-genes as a cell fate determinant in the developing central nervous system.

2005

The mechanisms controlling the generation of cell diversity in the central nervous system belong to the major unsolved problems in developmental biology. The fly Drosophila melanogaster is a suitable model system to examine these mechanisms at the level of individually identifiable cells. Recently, we have provided evidence that CyclinE--largely independent of its role in cell proliferation--plays a critical role in the specification of neural stem cells (neuroblasts). CycE specifies neuronal fate within neuroblast lineages by acting upstream of glial factors (prospero and glial cell missing), whereby levels of CycE are controlled by homeotic genes, the master control genes regulating segme…

Central Nervous SystemCell fate determinationBiologyModels BiologicalNeuroblastCyclin EAnimalsHumansCell LineageHox geneMolecular BiologyGeneticsNeuronsStem CellsGenes HomeoboxGene Expression Regulation DevelopmentalCell Biologybiology.organism_classificationNeural stem cellCell biologyDrosophila melanogasterStem cellDrosophila melanogasterHomeotic geneDevelopmental biologyDevelopmental BiologyCell cycle (Georgetown, Tex.)
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A critical role for Cyclin E in cell fate determination in the central nervous system of Drosophila melanogaster

2004

We have examined the process by which cell diversity is generated in neuroblast (NB) lineages in the central nervous system of Drosophila melanogaster. Thoracic NB6-4 (NB6-4t) generates both neurons and glial cells, whereas NB6-4a generates only glial cells in abdominal segments. This is attributed to an asymmetric first division of NB6-4t, localizing prospero (pros) and glial cell missing (gcm) only to the glial precursor cell, and a symmetric division of NB6-4a, where both daughter cells express pros and gcm. Here we show that the NB6-4t lineage represents the ground state, which does not require the input of any homeotic gene, whereas the NB6-4a lineage is specified by the homeotic genes…

Central Nervous SystemCyclin ELineage (genetic)Cell divisionDown-RegulationNerve Tissue ProteinsCell fate determinationNeuroblastCyclin EAnimalsDrosophila ProteinsCell LineageHomeodomain ProteinsNeuronsbiologyStem CellsNeuropeptidesGenes HomeoboxGene Expression Regulation DevelopmentalNuclear ProteinsCell DifferentiationCell BiologyCell cyclebiology.organism_classificationGanglia InvertebrateCell biologyDNA-Binding ProteinsDrosophila melanogasterTrans-ActivatorsDrosophila melanogasterHomeotic geneNeurogliaTranscription FactorsNature Cell Biology
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Comm Sorts Robo to Control Axon Guidance at the Drosophila Midline

2002

AbstractAxon growth across the Drosophila midline requires Comm to downregulate Robo, the receptor for the midline repellent Slit. We show here that comm is required in neurons, not in midline cells as previously thought, and that it is expressed specifically and transiently in commissural neurons. Comm acts as a sorting receptor for Robo, diverting it from the synthetic to the late endocytic pathway. A conserved cytoplasmic LPSY motif is required for endosomal sorting of Comm in vitro and for Comm to downregulate Robo and promote midline crossing in vivo. Axon traffic at the CNS midline is thus controlled by the intracellular trafficking of the Robo guidance receptor, which in turn depends…

Central Nervous SystemEmbryo NonmammalianEndosomeGrowth ConesMolecular Sequence DataEndocytic cycleDown-RegulationNerve Tissue ProteinsReceptors Cell SurfaceCell CommunicationEndosomesBiologyModels BiologicalFunctional LateralityGeneral Biochemistry Genetics and Molecular BiologySequence Homology Nucleic AcidEctodermmedicineAnimalsDrosophila ProteinsReceptors ImmunologicAxonTransport VesiclesReceptorSequence Homology Amino AcidBiochemistry Genetics and Molecular Biology(all)Stem CellsCell MembraneGraft SurvivalGene Expression Regulation DevelopmentalMembrane ProteinsCell DifferentiationAnatomyCommissureSlitProtein Structure TertiaryCell biologyProtein TransportDrosophila melanogastermedicine.anatomical_structureCOS CellsRoundaboutAxon guidanceStem Cell TransplantationCell
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Compartmentalization of Central Neurons inDrosophila: A New Strategy of Mosaic Analysis Reveals Localization of Presynaptic Sites to Specific Segment…

2002

Synaptogenesis in the CNS has received far less attention than the development of neuromuscular synapses, although only central synapses allow the study of neuronal postsynaptic mechanisms and display a greater variety of structural and functional features. This neglect is attributable mainly to the enormous complexity of the CNS, which makes the visualization of individual synapses on defined neuronal processes very difficult. We overcome this obstacle and demonstrate by confocal microscopy the specific arrangement of output synapses on individual neurites. These studies are performed via genetic mosaic strategies in the CNS of the fruitfly Drosophila melanogaster. First, we use targeted e…

Central Nervous SystemEmbryo NonmammalianNeuropilNeuriteCell TransplantationTransport pathwaysPresynaptic TerminalsSynaptogenesisGene ExpressionNerve Tissue ProteinsBiologylaw.inventionGenes ReporterInterneuronsConfocal microscopylawPostsynaptic potentialNeuritesAnimalsCell LineageARTICLENeuronsTransplantation ChimeraMosaicismGeneral NeuroscienceGene targetingbiology.organism_classificationCell CompartmentationTransplantationDrosophila melanogasterGene TargetingMutationSynapsesDrosophila melanogasterNeuroscienceThe Journal of Neuroscience
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Spatio-temporal pattern of cells expressing the clock genes period and timeless and the lineages of period expressing neurons in the embryonic CNS of…

2010

The initial steps towards the generation of cell diversity in the central nervous system of the fruitfly Drosophila melanogaster take place during early phases of embryonic development when a stereotypic population of neural progenitor cells (neuroblasts and midline precursors) is formed in a precise spatial and temporal pattern, and subsequently expresses a particular sequence of genes. The clarification of the positional, temporal and molecular features of the individual progenitor cells in the nerve cord and brain as well as of their specific types of neuronal and/or glial progeny cells forms an essential basis to understand the mechanisms controlling their development. The present study…

Central Nervous SystemEmbryo NonmammalianTimelessPeriod (gene)PopulationModels BiologicalAnimals Genetically ModifiedNeuroblastCell MovementGeneticsAnimalsDrosophila ProteinsCell LineageeducationMolecular BiologyBody PatterningGeneticsNeuronseducation.field_of_studyLife Cycle StagesbiologyGene Expression Regulation DevelopmentalPeriod Circadian Proteinsbiology.organism_classificationNeural stem cellCell biologyClone CellsCLOCKDrosophila melanogasterLarvaDrosophila melanogasterNeural developmentDevelopmental BiologyGene expression patterns : GEP
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Tenectin, a novel extracellular matrix protein expressed during Drosophila melanogaster embryonic development

2006

1567-133X (Print) Journal Article Research Support, Non-U.S. Gov't; During Drosophila embryonic development, various morphogenetic processes require the remodeling of the extracellular matrix. In a previous study, we have identified and characterized a cDNA encoding a novel putative extracellular matrix protein named tenebrin, in the beetle Tenebrio molitor. Here, we examine the expression of the Drosophila ortholog, referred to as Tenectin (Tnc), during embryonic development. Tnc is expressed in the majority of tissues of neuroectodermic origin such as hindgut, foregut, tracheal system, anal plate, and CNS. In the CNS, the Tnc transcript is restricted to a few cells, whereas the protein is…

Central Nervous SystemEmbryo Nonmammaliananimal structuresEmbryonic DevelopmentIn situ hybridizationModels BiologicalExtracellular matrixModelsComplementary DNAGeneticsDrosophila ProteinsAnimalsDevelopmentalMolecular BiologyRegulation of gene expressionExtracellular Matrix ProteinsDrosophila Proteins/*metabolismNonmammalianbiologyExtracellular Matrix Proteins/*metabolismEmbryogenesisGene Expression Regulation DevelopmentalHindgutForegutGastrulabiology.organism_classificationmusculoskeletal systemBiologicalMolecular biologyTracheaCentral Nervous System/embryology/metabolismDrosophila melanogasterGene Expression RegulationEmbryoGastrula/metabolismembryonic structuresDrosophila melanogaster/*embryology/*metabolismDrosophila melanogasterTrachea/cytology/embryology/metabolismDevelopmental Biology
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Abdominal-A mediated repression of Cyclin E expression during cell-fate specification in the Drosophila central nervous system

2009

Homeotic/Hox genes are known to specify a given developmental pathway by regulating the expression of downstream effector genes. During embryonic CNS development of Drosophila, the Hox protein Abdominal-A (AbdA) is required for the specification of the abdominal NB6-4 lineage. It does so by down regulating the expression of the cell cycle regulator gene Dcyclin E (CycE). CycE is normally expressed in the thoracic NB6-4 lineage to give rise to mixed lineage of neurons and glia, while only glial cells are produced from the abdominal NB6-4 lineage due to the repression of CycE by AbdA. Here we investigate how AbdA represses the expression of CycE to define the abdominal fate of a single NB6-4 …

Central Nervous SystemEmbryologyTranscription GeneticRegulatorCell fate determinationBiologyAnimals Genetically ModifiedCyclin EAnimalsCell LineageTransgenesEnhancerHox genePsychological repressionIn Situ HybridizationRegulator geneHomeodomain ProteinsNeuronsGene Expression Regulation DevelopmentalCell DifferentiationCell cycleMolecular biologyCell biologyDrosophila melanogasterHomeotic geneNeurogliaDevelopmental BiologyMechanisms of Development
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