Search results for "sequence data"

showing 10 items of 1952 documents

Organization and expression of the chum salmon insulin-like growth factor II gene

1997

AbstractIGF-II plays an important role in growth and development of vertebrates. In the present study, the characterization of the first fish IGF-II gene, chum salmon IGF-II, is described. The sIGF-II gene consists of four exons, spanning a region of 9 kbp, that encode the 214 aa IGF-II precursor. While the amino acid sequences of fully processed IGF-II of salmon and mammalian species are very similar, the prepro-peptide sequence deviates extensively in the signal- and E-peptide domains. The transcription initiation site of the sIGF-II gene was localized within a 30 nt region employing RT-PCR. Using sIGF-II promoter-luciferase constructs it was demonstrated that the sIGF-II gene has a relat…

Untranslated regionBase pairMolecular Sequence DataBiophysicsBiologyTransfectionPolymerase Chain ReactionBiochemistryExonSalmonStructural BiologyGene expressionTumor Cells CulturedGeneticsAnimalsHumansProtein PrecursorsPromoter Regions GeneticInsulin-like growth factor IIMolecular BiologyGeneDNA PrimersGeneticsRegulation of gene expressionchemistry.chemical_classificationBase SequencefungiExonsCell BiologyTransfectionRecombinant ProteinsAmino acidGene structureOncorhynchus ketaFishGene Expression RegulationchemistryOncorhynchus mykissGene expressionFEBS Letters
researchProduct

Specific sequence elements in the 5′ untranslated regions of rbcL and atpB gene mRNAs stabilize transcripts in the chloroplast of Chlamydomonas reinh…

2001

Using a series of point mutations in chimeric reporter gene constructs consisting of the 5' regions of the Chlamydomonas chloroplast rbcL or atpB genes fused 5' to the coding sequence of the bacterial uidA (GUS) gene, RNA-stabilizing sequence elements were identified in vivo in the 5' untranslated regions (5' UTRs) of transcripts of the chloroplast genes rbcL and atpB in Chlamydomonas reinhardtii. In chimeric rbcL 5' UTR:GUS transcripts, replacement of single nucleotides in the 10-nt sequence 5'-AUUUCCGGAC-3', extending from positions +38 to +47 relative to the transcripts' 5' terminus, shortened transcript longevity and led to a reduction in transcript abundance of more than 95%. A similar…

Untranslated regionChloroplastsLightMolecular Sequence DataChlamydomonas reinhardtiiNucleic acid secondary structureAnimalsCoding regionRNA MessengerMolecular BiologyGeneGeneticsReporter geneBase SequencebiologyChlamydomonasRNADarknessbiology.organism_classificationMolecular biologyGenes BacterialMutagenesisNucleic Acid Conformation5' Untranslated RegionsChlamydomonas reinhardtiiResearch ArticleRNA
researchProduct

Changes in the 5?-untranslated region of the rbcL gene accelerate transcript degradation more than 50-fold in the chloroplast of Chlamydomonas reinha…

2003

Using uidA (beta-glucuronidase; GUS) reporter gene constructs, the 5'-untranslated region (UTR) of the Chlamydomonas chloroplast rbcL gene was screened by deletion and mutational analysis for the presence of a promoter element that previous studies implied to reside within the first 63 base pairs of the UTR. Deleting a large segment of the rbcL 5'UTR in a 3'--5' direction to position +36, changing the remaining 36 base pairs at the 5' end of the UTR, and increasing by five base pairs the distance between the rbcL 5'UTR and the basic promoter element located at position -10 did not abolish transcription from the basic rbcL promoter. It is concluded that the apparent loss of transcriptional a…

Untranslated regionChloroplastsTranscription GeneticFive prime untranslated regionBase pairRNA StabilityRibulose-Bisphosphate CarboxylaseMolecular Sequence DataChlamydomonas reinhardtiiPolymerase Chain ReactionTranscription (biology)GeneticsAnimalsPromoter Regions GeneticGeneSequence DeletionGeneticsReporter geneBase SequencebiologyChimeraChlamydomonasGeneral MedicineBlotting Northernbiology.organism_classificationMolecular biologyBlotting SouthernMutation5' Untranslated RegionsChlamydomonas reinhardtiiPlasmidsCurrent Genetics
researchProduct

Association of AUUUA-binding Protein with A + U-rich mRNA during nucleo-cytoplasmic transport

1992

Resealed nuclear envelope (NE) vesicles from rat liver containing entrapped exogenous RNA were used to study the effect of adenosine+uridine binding factor (AUBF), present in cytosolic cell extracts, on ATP-dependent transport of A+U-rich RNA (AU+RNA) and A+U-free RNA (AU-RNA) across the NE. This factor specifically binds to A+U-rich sequences present in the 3' untranslated regions of lymphokine and cytokine mRNAs, containing overlapping AUUUA boxes (granulocyte-macrophage colony stimulating factor, interleukin-3). Addition of AUBF to the extravesicular compartment markedly increased the efflux of the in vitro transcribed, capped and polyadenylated AU+ RNAs. Export of entrapped AU- control …

Untranslated regionCytoplasmAdenosineTranscription GeneticPolyadenylationNuclear EnvelopeMolecular Sequence DataRNA-binding proteinBiologyCell LineStructural BiologyTranscription (biology)EndoribonucleasesAnimalsHumansNuclear MatrixRNA MessengerBinding siteNuclear export signalUridineMolecular BiologyCell NucleusMessenger RNABinding SitesBase SequenceGranulocyte-Macrophage Colony-Stimulating FactorInterferon-alphaRNA-Binding ProteinsRNAMolecular biologyRatsKineticsLiverRibonucleoproteinsInterleukin-3Carrier ProteinsPlasmidsPolyribonucleotidesProtein BindingJournal of Molecular Biology
researchProduct

Nitric oxide increases the decay of matrix metalloproteinase 9 mRNA by inhibiting the expression of mRNA-stabilizing factor HuR.

2003

Dysregulation of extracellular matrix turnover is an important feature of many inflammatory processes. Rat renal mesangial cells express high levels of matrix metalloproteinase 9 (MMP-9) in response to inflammatory cytokines such as interleukin-1 beta. We demonstrate that NO does strongly destabilize MMP-9 mRNA, since different luciferase reporter gene constructs containing the MMP-9 3' untranslated region (UTR) displayed significant reduced luciferase activity in response to the presence of NO. Moreover, by use of an in vitro degradation assay we found that the cytoplasmic fractions of NO-treated cells contained a higher capacity to degrade MMP-9 transcripts than those obtained from contro…

Untranslated regionCytoplasmRNA StabilityMolecular Sequence DataGene ExpressionRNA-binding proteinBiologyKidneyNitric OxideELAV-Like Protein 1Gene expressionAnimalsElectrophoretic mobility shift assayNitric Oxide DonorsRNA MessengerEnzyme InhibitorsMolecular Biology3' Untranslated RegionsCyclic GMPCells CulturedRepetitive Sequences Nucleic AcidMessenger RNABase SequenceThree prime untranslated regionMolecular MimicryRNARNA-Binding ProteinsCell BiologyMolecular biologyRecombinant ProteinsRatsELAV ProteinsMatrix Metalloproteinase 9RibonucleoproteinsGuanylate CyclaseAntigens SurfaceAminoquinolinesDactinomycinSoluble guanylyl cyclaseInterleukin-1Nitroso CompoundsMolecular and cellular biology
researchProduct

The Suppressor of fused Gene Encodes a Novel PEST Protein Involved in Drosophila Segment Polarity Establishment

1995

Abstract Suppressor of fused, Su(fu), was identified as a semi-dominant suppressor of the putative serine/threonine kinase encoded by the segment polarity gene fused in Drosophila melanogaster. The amorphic Su(fu) mutation is viable, shows a maternal effect and displays no phenotype by itself. Su(fu) mutations are often found associated to karmoisin (kar) mutations but two complementation groups can be clearly identified. By using a differential hybridization screening method, we have cloned the Su(fu) region and identified chromosomal rearrangements associated with Su(fu) mutations. Two classes of cDNAs with similar developmental patterns, including a maternal contribution, are detectable …

Untranslated regionDNA Complementary[SDV]Life Sciences [q-bio]Recombinant Fusion ProteinsMolecular Sequence DataRestriction MappingInvestigations03 medical and health sciencesPEST sequence0302 clinical medicineTranscription (biology)GeneticsAnimalsDrosophila ProteinsAmino Acid SequenceCloning MolecularGenes SuppressorPeptide sequenceGeneGerm-Line MutationIn Situ Hybridization030304 developmental biologyGenetics0303 health sciencesBase SequencebiologyBlotting Northernbiology.organism_classificationMolecular biology[SDV] Life Sciences [q-bio]Repressor ProteinsComplementationDrosophila melanogasterPhenotypeSegment polarity geneDrosophila melanogaster030217 neurology & neurosurgery
researchProduct

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
researchProduct

Characterization of a new member of the sea urchin Paracentrotus lividus hsp70 gene family and its expression

1992

We have sequenced a second gene of the hsp70 family derived from a genomic clone of the sea urchin, Paracentrotus lividus. The structure of this gene, named hsp70IV gene, is interrupted by one intron and differs from the previously analyzed sea urchin hsp70II gene, which contains several introns. Two open reading frames of hsp70IV gene encode a predicted protein of 639 amino acids with an M(r) of 69,672. The 5' flanking region of the gene contains a putative TATA element, three heat-shock elements made up of some arrays of the 5-bp units, NGAAN and NTTCN (N = A,C,G or T), a canonic consensus sequence for binding of the regulatory activating transcription factor (ATF), and a purine box. The …

Untranslated regionHot TemperatureTranscription GeneticMolecular Sequence DataRestriction MappingGene ExpressionParacentrotus lividusExonGene expressionGene clusterGeneticsAnimalsAmino Acid SequenceRNA MessengerCloning MolecularPromoter Regions GeneticGeneHeat-Shock ProteinsGeneticsBase SequencebiologyIntronGeneral Medicinebiology.organism_classificationMolecular biologyIntronsOpen reading frameGenesMultigene FamilySea UrchinsGene
researchProduct

Nucleotide sequence of a ssRNA phage from Acinetobacter: kinship to coliphages.

2002

The complete nucleotide sequence of ssRNA phage AP205 propagating in Acinetobacter species is reported. The RNA has three large ORFs, which code for the following homologues of the RNA coliphage proteins: the maturation, coat and replicase proteins. Their gene order is the same as that in coliphages. RNA coliphages or Leviviridae fall into two genera: the alloleviviruses, like Qβ, which have a coat read-through protein, and the leviviruses, like MS2, which do not have this coat protein extension. AP205 has no read-through protein and may therefore be classified as a levivirus. A major digression from the known leviviruses is the apparent absence of a lysis gene in AP205 at the usual positio…

Untranslated regionMolecular Sequence DataRNA-dependent RNA polymeraseGenome ViralBiologyNucleic acid secondary structureOpen Reading FramesViral ProteinsCapsidVirologyLeviviridaeAmino Acid SequenceGene3' Untranslated RegionsPhylogenyGeneticsAcinetobacterBase SequenceAllolevivirusNucleic acid sequenceRNAbiology.organism_classificationVirologyLeviviridaeNucleic Acid ConformationSequence AlignmentThe Journal of general virology
researchProduct

Analysis of involvement of the 3?-untranslated regions in regulating mRNA stability for vitellogenin, cyanoprotein ?, and cyanoprotein ? from the bea…

2002

The degradation of the 3'-untranslated regions (UTRs) of vitellogenin, cyanoprotein alpha, and cyanoprotein beta from the bean bug, Riptortus clavatus, was analyzed in vitro. The degradation pattern was similar for all three RNAs, with a high degradation rate in non-diapausing adult insects and no degradation in the fifth instar nymphs and in diapausing adults, and was not correlated with the expression levels of these three proteins. Proteins binding to the 3'-UTRs were detected in polysomal and cytosolic extracts. These factors, however, were present in all developmental stages. The abundance of the polysomal factor showed little variation, but the cytosolic factor was enriched in adult i…

Untranslated regionPhysiologyMolecular Sequence DatahexamerinElectrophoretic Mobility Shift AssayRNA-binding proteinBinding CompetitiveBiochemistryHemipteraVitellogeninsVitellogeninBotanyAnimalsRNA Messenger3' Untranslated RegionsRegulation of gene expressionMessenger RNABase Sequencebiologyjuvenile hormoneThree prime untranslated regionRNA-Binding ProteinsRNAGeneral MedicineRNA binding proteincyanoproteindiapauseGene Expression RegulationBiochemistryInsect ScienceJuvenile hormonebiology.proteinInsect ProteinsSequence AlignmentArchives of Insect Biochemistry and Physiology
researchProduct