Search results for "Protein Biosynthesis"

showing 10 items of 220 documents

Expression patterns of matrix genes during human skeletal development.

1994

Extracellular Matrix ProteinsHistologyBone DevelopmentChemistryClinical BiochemistryCell DifferentiationCell BiologyComputational biologyExpression (computer science)Cartilage Oligomeric Matrix ProteinAlkaline PhosphataseMatrix (mathematics)Gene Expression RegulationProtein BiosynthesisBiglycanHumansMatrilin ProteinsLectins C-TypeOsteonectinProteoglycansAggrecansCollagenDecorinGeneGlycoproteinsProgress in histochemistry and cytochemistry
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Expression of the Anti-amyloidogenic Secretase ADAM10 Is Suppressed by Its 5′-Untranslated Region*

2010

Proteolytic processing of the amyloid precursor protein by alpha-secretase prevents formation of the amyloid beta-peptide (Abeta), which is the main constituent of amyloid plaques in brains of Alzheimer disease (AD) patients. alpha-Secretase activity is decreased in AD, and overexpression of the alpha-secretase ADAM10 (a disintegrin and metalloprotease 10) in an AD animal model prevents amyloid pathology. ADAM10 has a 444-nucleotide-long, very GC-rich 5'-untranslated region (5'-UTR) with two upstream open reading frames. Because similar properties of 5'-UTRs are found in transcripts of many genes, which are regulated by translational control mechanisms, we asked whether ADAM10 expression is…

Five prime untranslated regionenzymology [Brain]ADAM10ADAM10 protein humanBACE1-ASgenetics [Amyloid Precursor Protein Secretases]genetics [Alzheimer Disease]genetics [ADAM Proteins]BiochemistryGene Expression Regulation Enzymologicbiosynthesis [Membrane Proteins]ADAM10 ProteinAlzheimer DiseaseChlorocebus aethiopsAmyloid precursor proteinProtein biosynthesisbiosynthesis [Amyloid beta-Peptides]genetics [Amyloid beta-Peptides]AnimalsHumansGene RegulationMolecular BiologySequence Deletionbiosynthesis [ADAM Proteins]Amyloid beta-PeptidesbiologyBase SequenceP3 peptideenzymology [Alzheimer Disease]BrainMembrane ProteinsCell BiologyMolecular biologyBiochemistry of Alzheimer's diseasegenetics [Membrane Proteins]ADAM Proteinsbiosynthesis [Amyloid Precursor Protein Secretases]Protein Biosynthesisddc:540COS Cellsbiology.proteinAmyloid Precursor Protein Secretases5' Untranslated RegionsAmyloid precursor protein secretase
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The Effect of tRNA

2021

Transfer RNA[Ser]Sec carries multiple post-transcriptional modifications. The A37G mutation in tRNA[Ser]Sec abrogates isopentenylation of base 37 and has a profound effect on selenoprotein expression in mice. Patients with a homozygous pathogenic p.R323Q variant in tRNA-isopentenyl-transferase (TRIT1) show a severe neurological disorder, and hence we wondered whether selenoprotein expression was impaired. Patient fibroblasts with the homozygous p.R323Q variant did not show a general decrease in selenoprotein expression. However, recombinant human TRIT1R323Q had significantly diminished activities towards several tRNA substrates in vitro. We thus engineered mice conditionally deficient in Tr…

GPX1medicine.disease_causelaw.inventiontRNA<sup>[Ser]Sec</sup>MiceRNA TransferlawBiology (General)Trit1Selenoproteins<i>Trit1</i>Spectroscopychemistry.chemical_classificationNeuronsMutationChemistryTranslation (biology)General MedicineComputer Science ApplicationsBlotChemistryLiverTransfer RNARecombinant DNAQH301-705.5isopentenylationCatalysisArticleCell LineInorganic ChemistrySeleniumSelenoprotein PmedicineAnimalsHumansCysteinePhysical and Theoretical ChemistrytRNA[Ser]SecMolecular BiologyQD1-999Alkyl and Aryl TransferasesOrganic ChemistryPhosphotransferasesMolecular biologyIn vitroSelenocysteineProtein BiosynthesisHepatocytesSelenoproteinRibosomesInternational journal of molecular sciences
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Sch 9p kinase and the Gcn4p transcription factor regulate glycerol production during winemaking

2017

Grape juice fermentation is a harsh environment with many stressful conditions, and Saccharomyces cerevisiae adapts its metabolism in response to those environmental challenges. Many nutrient-sensing pathways control this feature. The Tor/Sch9p pathway promotes growth and protein synthesis when nutrients are plenty, while the transcription factor Gcn4p is required for the activation of amino acid biosynthetic pathways. We previously showed that Sch9p impact on longevity depends on the nitrogen/carbon ratio. When nitrogen is limiting, SCH9 deletion shortens chronological life span, which is the case under winemaking conditions. Its deletion also increases glycerol during fermentation, so the…

Gcn4pGlycerol0301 basic medicineSaccharomyces cerevisiae ProteinsWine yeastLongevitySaccharomyces cerevisiaeGene ExpressionSch9pWineSaccharomyces cerevisiaeProtein Serine-Threonine KinasesBiologyApplied Microbiology and BiotechnologyMicrobiology03 medical and health scienceschemistry.chemical_compoundGene Expression Regulation FungalGlycerolProtein biosynthesisMetabolomicsGlycolysisAmino acid synthesischemistry.chemical_classificationGene Expression ProfilingGeneral MedicineMetabolismbiology.organism_classificationAmino acidYeast in winemakingBasic-Leucine Zipper Transcription Factors030104 developmental biologychemistryBiochemistryFermentationGene DeletionFEMS Yeast Research
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An altered intracellular distribution of the autoantigen La/SS-B when translated from a La mRNA isoform.

1997

Abstract Transcription of the gene encoding for the nuclear autoantigen La resulted in La mRNA isoforms. A promoter switching combined with an alternative splicing pathway replaced exon 1 with exon 1′. Similar to mRNAs encoding for ribosomal proteins, exon 1′ started with a pyrimidine-rich 5′-terminus. Moreover, exon 1′ contained 5′-GC-rich regions and an oligo(U)-tail of 23 uridine residues. Exon 1′ encoded for three open reading frames upstream of the La protein reading frame. In spite of this unusual structure, exon 1′ La mRNAs were translated not only in vitro but also in transiently transfected cells. The translational efficiency of exon 1′ La mRNA was about 14% of exon 1 La mRNA using…

Gene isoformCytoplasmTranslational efficiencyDNA RecombinantBiologyTransfectionAutoantigensCell LineExonMiceExon trappingAnimalsHumansRNA MessengerGeneCell NucleusMessenger RNACell-Free SystemAlternative splicingCell Biology3T3 CellsExonsMolecular biologyOpen reading frameAlternative SplicingRibonucleoproteinsProtein BiosynthesisRabbitsExperimental cell research
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Regulation of the expression of inducible nitric oxide synthase

2004

The role of nitric oxide (NO) generated by the inducible isoform of nitric oxide synthase (iNOS) is very complex. Induction of iNOS expression and hence NO production has been described to have beneficial antiviral, antiparasital, microbicidal, immunomodulatory, and antitumoral effects. However, induced at the wrong place or at the wrong time, iNOS has detrimental consequences and seems to be involved in the pathophysiology of different human diseases. The pathways regulating iNOS expression seem to vary in different cells or different species. In general, activation of the transcription factors nuclear factor (NF)-kappaB and signal transducer and activator of transcription (STAT)-1alpha an…

Gene isoformTranscription GeneticNitric Oxide Synthase Type IIBiologyGene Expression Regulation EnzymologicstatNitric oxidechemistry.chemical_compoundAnimalsHumansRNA MessengerPromoter Regions GeneticTranscription factorPharmacologyRegulation of gene expressionMolecular biologyCell biologyNitric oxide synthasechemistryProtein BiosynthesisSTAT proteinbiology.proteinNitric Oxide SynthaseSignal transductionSignal TransductionTranscription FactorsEuropean Journal of Pharmacology
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Facilitating matched pairing and expression of TCR chains introduced into human T cells.

2006

AbstractAdoptive transfer of T lymphocytes is a promising treatment for a variety of malignancies but often not feasible due to difficulties generating T cells that are reactive with the targeted antigen from patients. To facilitate rapid generation of cells for therapy, T cells can be programmed with genes encoding the α and β chains of an antigen-specific T-cell receptor (TCR). However, such exogenous α and β chains can potentially assemble as pairs not only with each other but also with endogenous TCR α and β chains, thereby generating αβTCR pairs of unknown specificity as well as reducing the number of exogenous matched αβTCR pairs at the cell surface. We demonstrate that introducing cy…

GeneticsAdoptive cell transferTranscription GeneticCD3T-LymphocytesImmunologyGenetic transferT-cell receptorReceptors Antigen T-CellCell BiologyHematologyT lymphocyteGene TherapyBiologyBiochemistryCell biologyCell LineAntigenCell cultureProtein Biosynthesisbiology.proteinHumansCysteineReceptorBlood
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Long-range translational coupling in single-stranded RNA bacteriophages: an evolutionary analysis

1998

In coliphage MS2 RNA a long-distance interaction (LDI) between an internal segment of the upstream coat gene and the start region of the replicase gene prevents initiation of replicase synthesis in the absence of coat gene translation. Elongating ribosomes break up the repressor LDI and thus activate the hidden initiation site. Expression studies on partial MS2 cDNA clones identified base pairing between 1427-1433 and 1738-1744, the so-called Min Jou (MJ) interaction, as the molecular basis for the long-range coupling mechanism. Here, we examine the biological significance of this interaction for the control of replicase gene translation. The LDI was disrupted by mutations in the 3'-side an…

GeneticsBase SequenceBase pairRNARepressorRNA-dependent RNA polymeraseTranslation (biology)RNA PhagesBiologyRNA-Dependent RNA PolymeraseRibosomeEvolution MolecularProtein BiosynthesisGeneticsProtein biosynthesisNucleic Acid ConformationRNA ViralGeneResearch ArticlePlasmidsNucleic Acids Research
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Rapid evolution of translational control mechanisms in RNA genomes

1997

We have introduced 13 base substitutions into the coat protein gene of RNA bacteriophage MS2. The mutations, which are clustered ahead of the overlapping lysis cistron, do not change the amino acid sequence of the coat protein, but they disrupt a local hairpin, which is needed to control translation of the lysis gene. The mutations decreased the phage titer by four orders of magnitude but, upon passaging, the virus accumulated suppressor mutations that raised the fitness to almost wild-type level. Analysis of the pseudorevertants showed that the disruption of the local hairpin, controlling expression of the lysis gene, had apparently been so complete that its restoration by chance mutations…

GeneticsGenomeBase SequenceGenes ViralbiologyMolecular Sequence DataRNAMutagenesis (molecular biology technique)RNA virusbiology.organism_classificationNucleic acid secondary structureEvolution MolecularCapsidCistronMutagenesisStructural BiologyProtein BiosynthesisBacteriophage MS2Protein biosynthesisNucleic Acid ConformationRNA ViralMolecular BiologyGeneLevivirusJournal of Molecular Biology
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Forced Retroevolution of an RNA Bacteriophage

2000

AbstractThe operator hairpin ahead of the replicase gene in RNA bacteriophage MS2 contains overlapping signals for binding the coat protein and ribosomes. Coat protein binding inhibits further translation of the gene and forms the first step in capsid formation. The hairpin sequence was partially randomized to assess the importance of this structure element for the bacteriophage and to monitor alternative solutions that would evolve on the passaging of mutant phages. The evolutionary reconstruction of the operator failed in the majority of mutants. Instead, a poor imitation developed containing only some of the recognition signals for the coat protein. Three mutants were of particular inter…

GeneticsOperator Regions GeneticBase SequencebiologyMolecular Sequence DataRNARNA-dependent RNA polymeraseRNA-Dependent RNA Polymerasebiology.organism_classificationRibosomeStop codonEvolution MolecularBacteriophageSense CodonCodon NonsenseMutagenesisProtein BiosynthesisVirologyBacteriophage MS2Nucleic Acid ConformationGeneLevivirusVirology
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