Search results for "Photoreceptor"

showing 10 items of 143 documents

Phosphorylation of the Usher syndrome 1G protein SANS controls Magi2-mediated endocytosis.

2014

Item does not contain fulltext The human Usher syndrome (USH) is a complex ciliopathy with at least 12 chromosomal loci assigned to three clinical subtypes, USH1-3. The heterogeneous USH proteins are organized into protein networks. Here, we identified Magi2 (membrane-associated guanylate kinase inverted-2) as a new component of the USH protein interactome, binding to the multifunctional scaffold protein SANS (USH1G). We showed that the SANS-Magi2 complex assembly is regulated by the phosphorylation of an internal PDZ-binding motif in the sterile alpha motif domain of SANS by the protein kinase CK2. We affirmed Magi2's role in receptor-mediated, clathrin-dependent endocytosis and showed tha…

Scaffold proteinGuanylate kinaseMolecular Sequence DataPrimary Cell CultureNerve Tissue ProteinsBiologyEndocytosisPhotoreceptor cellExocytosisMiceCiliogenesisGeneticsmedicineAnimalsHumansProtein Interaction Domains and MotifsAmino Acid SequencePhosphorylationRNA Small InterferingSensory disorders Radboud Institute for Molecular Life Sciences [Radboudumc 12]Molecular BiologyGenetics (clinical)Adaptor Proteins Signal TransducingBinding SitesGeneral MedicineClathrinEndocytosisCell biologyMice Inbred C57BLRenal disorders Radboud Institute for Molecular Life Sciences [Radboudumc 11]medicine.anatomical_structureHEK293 CellsGene Expression RegulationCiliary pocketCarrier ProteinsSterile alpha motifGuanylate KinasesSequence AlignmentUsher SyndromesPhotoreceptor Cells VertebrateProtein BindingSignal TransductionHuman molecular genetics
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Direct binding of Magi2 to the USH1G protein SANS links the periciliary USH protein network to endocytosis

2012

The human Usher syndrome (USH) is the most common form of combined deaf-blindness. The encoded molecules are integrated into protein networks by scaffolds including the USH1G protein SANS (scaffold protein containing ankyrin repeats and SAM domain). Previous studies indicated SANS´ participation in vesicle transport and cargo handover at the periciliary region of photoreceptor cells. To decipher the precise cellular role of SANS, we searched for interacting partners. Therefore we adopted a yeast-2-hybrid screen of a retinal cDNA library using SANS´ C-terminus as bait. Amongst others we identified the MAGUK protein Magi2 (membrane-associated guanylate kinase inverted-2) as putative binding p…

Scaffold proteinImmunoelectron microscopyCell BiologyBiologyEndocytosisInteractomePhotoreceptor cellCell biologyVesicular transport proteinmedicine.anatomical_structureCiliary pocketPoster PresentationmedicineAnkyrin repeatCilia
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Evidence for synergistic and complementary roles of Bassoon and darkness in organizing the ribbon synapse

2012

Abstract Ribbon synapses are tonically active high-throughput synapses. The performance of the ribbon synapse is accomplished by a specialization of the cytomatrix at the active zone (CAZ) referred to as the synaptic ribbon (SR). Progress in our understanding of the structure–function relationship at the ribbon synapse has come from observations that, in photoreceptors lacking a full-size scaffolding protein Bassoon ( Bsn Δ Ex 4 / 5 ), dissociation of SRs coincides with perturbed signal transfer. The aim of the present study has been to elaborate the role of Bassoon as a structural organizer of the ribbon synapse and to differentiate it with regard to the ambient lighting conditions. The ul…

Scaffold proteinSynaptic ribbonRetinaGeneral NeuroscienceNerve Tissue ProteinsNanotechnologyDarknessRibbon synapseBiologyMice Mutant StrainsMice Inbred C57BLMicemedicine.anatomical_structureMicroscopy Electron TransmissionArciform densitySynapsesDarknessRibbonmedicineBiophysicsAnimalssense organsActive zonePhotoreceptor Cells VertebrateNeuroscience
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Direct interaction of the Usher syndrome 1G protein SANS and myomegalin in the retina

2011

Contains fulltext : 96822.pdf (Publisher’s version ) (Closed access) The human Usher syndrome (USH) is the most frequent cause of combined hereditary deaf-blindness. USH is genetically heterogeneous with at least 11 chromosomal loci assigned to 3 clinical types, USH1-3. We have previously demonstrated that all USH1 and 2 proteins in the eye and the inner ear are organized into protein networks by scaffold proteins. This has contributed essentially to our current understanding of the function of USH proteins and explains why defects in proteins of different families cause very similar phenotypes. We have previously shown that the USH1G protein SANS (scaffold protein containing ankyrin repeat…

Scaffold proteinUsher syndromePhosphodiesterase 4D interacting protein (PDE4DIP)Muscle ProteinsPlasma protein bindingMice0302 clinical medicineYeastsChlorocebus aethiopsNuclear proteinCells CulturedGenetics0303 health scienceseducation.field_of_studyNuclear ProteinsCell biologyCOS CellssymbolsPhotoreceptor Cells VertebrateProtein BindingMicrotubule based transportNerve Tissue ProteinsBiologyModels BiologicalRetina03 medical and health sciencessymbols.namesakemedicineAnimalsHumanseducationMolecular BiologyAdaptor Proteins Signal Transducing030304 developmental biologyCell BiologyGlycostation disorders [IGMD 4]Golgi apparatusmedicine.diseaseMacaca mulattaMice Inbred C57BLCytoskeletal ProteinsPhotoreceptor cell functionMyomegalinGenetics and epigenetic pathways of disease Functional Neurogenomics [NCMLS 6]CattleAnkyrin repeatCiliary baseIntracellular transport030217 neurology & neurosurgerySensorineuronal degeneration
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Nxnl2 splicing results in dual functions in neuronal cell survival and maintenance of cell integrity

2012

International audience; The rod-derived cone viability factors, RdCVF and RdCVF2, have potential therapeutical interests for the treatment of inherited photoreceptor degenerations. In the mouse lacking Nxnl2, the gene encoding RdCVF2, the progressive decline of the visual performance of the cones in parallel with their degeneration, arises due to the loss of trophic support from RdCVF2. In contrary, the progressive loss of rod visual function of the Nxnl2-/- mouse results from a decrease in outer segment length, mediated by a cell autonomous mechanism involving the putative thioredoxin protein RdCVF2L, the second spliced product of the Nxnl2 gene. This novel signaling mechanism extends to o…

Sensory Receptor Cellsgenetic structuresCell SurvivalRNA SplicingSensory system[SDV.GEN] Life Sciences [q-bio]/GeneticsOlfactionBiologyArticleMice03 medical and health sciencesThioredoxins0302 clinical medicineRetinal Rod Photoreceptor CellsGeneticsAnimalsEye ProteinsMolecular BiologyGeneCells CulturedGenetics (clinical)030304 developmental biology[SDV.GEN]Life Sciences [q-bio]/Genetics0303 health sciencesGeneral MedicineAnatomySensory Receptor CellsCell biologyRNA splicingThioredoxinRetinal Rod Photoreceptor Cells030217 neurology & neurosurgeryFunction (biology)Human Molecular Genetics
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Polyamines and ripening of photoreceptor outer-segment in chicken embryo.

1995

Polyamines and their related monoacetyl derivatives were studied in rod outer segment (ROS) and cone outer segment (COS) of photoreceptor cells from chick embryo retina during eye development (7th-18th days). Putrescine was found to be necessary, in the second phase of retinogenesis, to sustain both ROS and COS differentiation and, after acetylation, gamma-aminobutyric acid synthesis. On the Other hand, spermidine and even more spermine intervene in the third phase of development when photoreceptors mature. Moreover, the presence of Nl-acetylspermidine already at the 7th day indicates that in the outer segment of photoreceptor cells too, as in the whole retina, putrescine synthesis comes ab…

Settore BIO/10 - Biochimicapolyamines monoacetylpolyamines GABA chick embryo retina outer segment photoreceptors retina differentiation
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ERG signal analysis using wavelet transform

2009

The wavelet analysis is a powerful tool for analyzing and detecting features of signals characterized by time-dependent statistical properties, as biomedical signals. The identification and the analysis of the components of these signals in the time-frequency domain, give meaningful information about the physiological mechanisms that govern them. This article presents the results of the wavelet analysis applied to the a-wave component of the human electroretinogram. In order to deepen and improve our knowledge about the behavior of the early photoreceptoral response, including the possible activation of interactions and correlations among the photoreceptors, we have detected and identified …

Statistics and ProbabilitySignal processingComputer scienceApplied MathematicsWavelet AnalysisMexican hat waveletWavelet transformLuminanceRetinaSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Electroretinogram – a-wave – Photoreceptoral response – Wavelet analysis – Mexican hat waveletRange (mathematics)Identification (information)WaveletOrder (biology)ElectroretinographyHumansPhotoreceptor CellsBiological systemPhotic StimulationEcology Evolution Behavior and SystematicsTheory in Biosciences
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Taurine in the interphotoreceptor matrix

2014

TAURINE IN THE INTERPHOTORECEPTOR MATRIX Gueli Maria Concetta Dipartimento di Biomedicina Sperimentale e Neuroscienze Cliniche (BioNEC), Università degli Studi di Palermo Taurine (Tau) is the most abundant amino compound free in the retina. It is concentrated in the photoreceptor inner segment, in the outer nuclear layer and in the synapses. The retina synthesizes and receives Tau from choroidal blood via the pigment epithelium (PE). The high content in the retina suggest the possibily of verifying whether it was present in the interphotoreceptor matrix (IPM), which occupies the subretinal space. In this study we have determined the Tau level in the IPM, separating it from other soluble ami…

Taurine interphotoreceptor matrix retina pigment epitheliumSettore BIO/10 - Biochimica
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Molecular mechanisms in developmental biology.

1996

Some general molecular mechanisms underlying development are described. Namely: those involved in the differentiation of the R7 receptor in Drosophila embryonic retina; those involved in the determination of embryonic axes and in polar cell differentiation, in Drosophila; those involved in the determination of the AB and P cell lineage and in vulva differentiation in Caenorhabditis embryos.

animal structuresbiologyCellular differentiationfungiEmbryoCell BiologyGeneral Medicinebiology.organism_classificationEmbryonic stem cellCell biologyVulvaCaenorhabditisAnimalsRNADrosophilaFemalePhotoreceptor CellsSignal transductionDrosophila (subgenus)Caenorhabditis elegansDevelopmental biologyMolecular BiologyCaenorhabditis elegansDevelopmental BiologyCell biology international
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The binding of G-protein to rod outer segment phospholipids at the nitrogen–water interface

1989

In the visual process, one photoexcited rhodopsin (R*) catalyzes the activation of hundreds of G-proteins. It remains to be determined whether G-protein and R* find one another by membrane surface diffusion of these components (diffusion model) or by diffusion of G-protein through the aqueous phase (hopping model). A monolayer of each main rod outer segment (ROS) phospholipid interacting with a subphase containing G-protein, has been used to simulate the interaction of G-protein with the cytoplasmic surface of discal membranes. The possible diffusion of G-protein through the aqueous phase was then measured by observing its adsorption–desorption in the monolayer of each main ROS phospholipi…

biologyChemistryAqueous two-phase systemPhospholipidMembrane ProteinsCell BiologySurface pressureBiochemistryCrystallographychemistry.chemical_compoundMembraneGTP-Binding ProteinsCytoplasmRhodopsinMonolayerbiology.proteinAnimalsCattlePhotoreceptor CellsDiffusion (business)Molecular BiologyPhospholipidsBiochemistry and Cell Biology
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