Search results for "Sequence analysi"

showing 10 items of 1351 documents

Selection on Coding Regions Determined Hox7 Genes Evolution

2003

The important role of Hox genes in determining the regionalization of the body plan of the vertebrates makes them invaluable candidates for evolutionary analyses regarding functional and morphological innovation. Gene duplication and gene loss led to a variable number of Hox genes in different vertebrate lineages. The evolutionary forces determining the conservation or loss of Hox genes are poorly understood. In this study, we show that variable selective pressures acted on Hox7 genes in different evolutionary lineages, with episodes of positive selection occurring after gene duplications. Tests for functional divergence in paralogs detected significant differentiation in a region known to …

Molecular Sequence DataBiologyEvolution MolecularOpen Reading FramesNegative selectionGene DuplicationGene duplicationGene clusterGeneticsAnimalsHumansCoding regionAmino Acid SequenceHox geneMolecular BiologyGenePhylogenyEcology Evolution Behavior and SystematicsGeneticsLikelihood FunctionsGenes HomeoboxGenetic VariationSequence Analysis DNABody planEvolutionary biologyMultigene FamilyVertebratesFunctional divergenceMolecular Biology and Evolution
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Isolation and Characterization of Novosphingobium sp. Strain MT1, a Dominant Polychlorophenol-Degrading Strain in a Groundwater Bioremediation System

2002

ABSTRACT A high-rate fluidized-bed bioreactor has been treating polychlorophenol-contaminated groundwater in southern Finland at 5 to 8°C for over 6 years. We examined the microbial diversity of the bioreactor using three 16S ribosomal DNA (rDNA)-based methods: denaturing gradient gel electrophoresis, length heterogeneity-PCR analysis, and restriction fragment length polymorphism analysis. The molecular study revealed that the process was dependent on a stable bacterial community with low species diversity. The dominant organism, Novosphingobium sp. strain MT1, was isolated and characterized. Novosphingobium sp. strain MT1 degraded the main contaminants of the groundwater, 2,4,6-trichloroph…

Molecular Sequence DataFresh WaterDNA RibosomalPolymerase Chain ReactionApplied Microbiology and BiotechnologyMixed Function OxygenasesMicrobiologyBioreactorsBioremediationRNA Ribosomal 16SEnvironmental Microbiology and BiodegradationRibosomal DNAAlphaproteobacteriaSphingobium chlorophenolicumElectrophoresis Agar GelGeneticsEcologyStrain (chemistry)biologyAlphaproteobacteriaGenes rRNASequence Analysis DNA16S ribosomal RNAbiology.organism_classificationBiodegradation EnvironmentalRestriction fragment length polymorphismPolymorphism Restriction Fragment LengthWater Pollutants ChemicalTemperature gradient gel electrophoresisChlorophenolsFood ScienceBiotechnologyApplied and Environmental Microbiology
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Receptor protein-tyrosine phosphatases: origin of domains (catalytic domain, Ig-related domain, fibronectin type III module) based on the sequence of…

2001

Abstract Reversible tyrosine phosphorylation of proteins is one of the major regulatory physiological events in response to cell-cell- and cell-matrix contact in Metazoa. Previously it was documented that the tyrosine phosphorylating enzymes, the tyrosine kinases (TKs), are autapomorphic characters of Metazoa, including sponges. In this paper the tyrosine dephosphorylating enzymes, the protein-tyrosine phosphatases (PTPs), are studied which can be grouped into two subfamilies, the soluble PTPs and the receptor PTPs (RPTPs). PTPs are characterized by one PTPase domain which interestingly comprises sequence similarity to yeast PTPs. In contrast to the PTPs, the RPTPs – which have been found o…

Molecular Sequence DataImmunoglobulinsBiologyPolymerase Chain ReactionEvolution Molecularchemistry.chemical_compoundCatalytic DomainGene duplicationGeneticsAnimalsAmino Acid SequenceTyrosineCloning MolecularPhylogenychemistry.chemical_classificationPhylogenetic treeSequence Homology Amino AcidTyrosine phosphorylationGeneral MedicineProtein-Tyrosine KinasesAmino acidFibronectinsPoriferaProtein Structure TertiaryOpen reading framechemistryBiochemistryPhosphorylationProtein Tyrosine PhosphatasesTyrosine kinaseSequence AnalysisGene
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Expression of one sponge Iroquois homeobox gene in primmorphs from Suberites domuncula during canal formation

2003

SUMMARY Sponges (Porifera) represent the evolutionary oldest multicellular animals. They are provided with the basic molecules involved in cell–cell and cell–matrix interactions. We report here the isolation and characterization of a complementary DNA from the sponge Suberites domuncula coding for the sponge homeobox gene, SUBDOIRX-a. The deduced polypeptide with a predicted Mr of 44,375 possesses the highly conserved Iroquois-homeodomain. We applied in situ hybridization to localize Iroquois in the sponge. The expression of this gene is highest in cells adjacent to the canals of the sponge in the medulla region. To study the expression of Iroquois during development, the in vitro primmorph…

Molecular Sequence DataIn situ hybridizationFerric CompoundsComplementary DNAAnimalsCluster AnalysisGeneIn Situ HybridizationPhylogenyEcology Evolution Behavior and SystematicsDNA PrimersBase SequencebiologyMulticellular animalsGene Expression ProfilingGenes HomeoboxFresh-water sponge. Geodia-cydonium. Marine sponges. Ephydatia-muelleri. Adhesion receptors. Family. Origin. Cells. Identification. Evolution.Sequence Analysis DNAAnatomyBlotting Northernbiology.organism_classificationIn vitroPoriferaCell biologySuberites domunculaSpongeHomeoboxDevelopmental BiologyEvolution and Development
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Nereida ignava gen. nov., sp. nov., a novel aerobic marine alpha-proteobacterium that is closely related to uncultured Prionitis (alga) gall symbiont…

2005

A Gram-negative, slightly halophilic, non-pigmented, strictly aerobic, chemo-organotrophic bacterium was isolated from Mediterranean sea water off the Spanish coast near Valencia. This strain was poorly reactive, being unable to grow in most carbon sources analysed in minimal medium. However, good growth was observed when more complex media and longer incubation times were used. Phylogenetic analysis based on an almost complete 16S rRNA gene sequence placed strain 2SM4T within the Roseobacter group, in the vicinity of uncultured bacteria described as gall symbionts of several species of the red alga Prionitis. Sequence similarity values between strain 2SM4T and the closest neighbouring spec…

Molecular Sequence DataMicrobiologyDNA RibosomalPhylogeneticsRNA Ribosomal 16SBotanyMediterranean SeaSeawaterSymbiosisEcology Evolution Behavior and SystematicsPhylogenyAlphaproteobacteriaPhylogenetic treebiologyFatty AcidsAlphaproteobacteriaGeneral MedicineSequence Analysis DNARoseobacterRibosomal RNA16S ribosomal RNAbiology.organism_classificationRoseobacterHalophileAerobiosisCulture MediaRhodophytaTaxonomy (biology)International journal of systematic and evolutionary microbiology
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Cloning of a DNA fragment encoding part of a 70-kDa heat shock protein ofCandida albicans

1995

Immunoscreening of a mycelial expression library with polyclonal antibodies raised against mycelial cell wall resulted in the detection of a cDNA encoding a heat shock protein of Candida albicans. Sequence analysis of a 0.8-kb cDNA subclone, 2M-1, revealed an open reading frame encoding 244 amino acids. Southern blot analysis with this fragment as a probe demonstrated hybridization to C. albicans DNA. Northern analysis showed a substantial increase in 2M RNA expression levels after cells were subjected to heat shock. Western blot analysis with 2M monospecific antibodies recognized a 70-kDa protein which was present in membrane particles and cytosolic fractions.

Molecular Sequence DataMicrobiologyWestern blotImmunoscreeningHeat shock proteinComplementary DNACandida albicansGeneticsmedicineHSP70 Heat-Shock ProteinsAmino Acid SequenceRNA MessengerCloning MolecularHeat shockDNA FungalCandida albicansMolecular BiologySouthern blotBase Sequencebiologymedicine.diagnostic_testChromosome MappingSequence Analysis DNAbiology.organism_classificationMolecular biologyBiochemistryPolyclonal antibodiesbiology.proteinFEMS Microbiology Letters
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Cloning and characterization of PRB1, a Candida albicans gene encoding a putative novel endoprotease B and factors affecting its expression

2002

Abstract Several cDNA fragments corresponding to transcripts differentially expressed under conditions that favor mycelial growth of Candida albicans were identified by the “differential display” technique. One of these was cloned and used as a probe to rescue the full gene from a genomic library of the fungus. The sequence identified a single, uninterrupted open reading frame of 1395 nucleotides encoding a putative protein of 465 residues and a theoretical molecular weight of 50.3 kDa, present in the genome as a single copy located at chromosome 2 in different strains. The gene product showed high homology with subtilisin-like proteases, mainly PRB1, the vacuolar B protease from Saccharomy…

Molecular Sequence DataMutantCatabolite repressionMicrobiologyFungal ProteinsGene productGene Expression Regulation FungalComplementary DNACandida albicansHumansAmino Acid SequenceCloning MolecularDNA FungalCandida albicansMolecular BiologyGeneGene LibraryDifferential displayBase SequencebiologyGene Expression ProfilingSerine EndopeptidasesSequence Analysis DNAGeneral Medicinebiology.organism_classificationMolecular biologyElectrophoresis Gel Pulsed-FieldBlotting SouthernOpen reading frameBiochemistryMutagenesisChromosomes FungalSequence AlignmentResearch in Microbiology
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Characterization of the hemoglobin of the backswimmer Anisops deanei (Hemiptera).

2012

Abstract While O 2 -binding hemoglobin-like proteins are present in many insects, prominent amounts of hemoglobin have only been found in a few species. Backswimmers of the genera Anisops and Buenoa (Notonectidae) have high concentrations of hemoglobin in the large tracheal cells of the abdomen. Oxygen from the hemoglobin is delivered to a gas bubble and controls the buoyant density, which enables the bugs to maintain their position without swimming and to remain stationary in the mid-water zone where they hunt for prey. We have obtained the cDNA sequences of three Anisops deanei hemoglobin chains by RT-PCR and RACE techniques. The deduced amino acid sequences show an unusual insertion of a…

Molecular Sequence DataNotonectidaeLigandsBiochemistrylaw.inventionHemipteraHemoglobinslawComplementary DNAAnimalsHumansGlobinAmino Acid SequenceMolecular BiologyPhylogenychemistry.chemical_classificationbiologyHeteropteraSequence Analysis DNAbiology.organism_classificationHemipteraBiological EvolutionAmino acidOxygenKineticschemistryBiochemistryInsect ScienceRecombinant DNAInsect ProteinsHemoglobinInsect biochemistry and molecular biology
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Mapping of a binding site for ATP within the extracellular region of the Torpedo nicotinic acetylcholine receptor beta-subunit.

1997

Using 2,8,5'-[H-3]ATP as a direct photoaffinity label for membrane-bound nicotinic acetylcholine receptor (nAChR) from Torpedo marmorata, we have identified a binding site for ATP in the extracellular region of the beta-subunit of the receptor. Photolabeling was completely inhibited in the presence of saturating concentrations of nonradioactive ATP, whereas neither the purinoreceptor antagonists suramin, theophyllin, and caffeine nor the nAChR antagonists alpha-bungarotoxin and d-tubocurarine affected the labeling reaction. Competitive and noncompetitive nicotinic agonists and Ca2+ increased the yield of the photoreaction by up to 50%, suggesting that the respective binding sites are allost…

Molecular Sequence DataPhotoaffinity LabelsReceptors NicotinicTorpedoTritiumBiochemistryPeptide Mappingchemistry.chemical_compoundGanglion type nicotinic receptorAdenosine TriphosphateAdenine nucleotideAnimalsChymotrypsinTrypsinAmino Acid SequenceBinding siteBinding SitesbiologyHydrolysisCell MembranePeptide FragmentsNicotinic acetylcholine receptorNicotinic agonistBiochemistrychemistrybiology.proteinAlpha-4 beta-2 nicotinic receptorExtracellular SpaceAdenosine triphosphateSequence AnalysisATP synthase alpha/beta subunitsBiochemistry
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Engineering a 2D protein-DNA crystal.

2005

(Figure Presented) Weaving with DNA: A DNA-binding protein was used to control the structure of a self-assembled 2D crystal. In the absence of protein, four oligonucleotides hybridize to form a Kagome lattice of interwoven double helices with p3 symmetry (see image). Addition of protein RuvA during assembly changes the symmetry and connectivity to give a DNA-protein crystal with an approximately square unit cell. © 2005 Wiley-VCH Verlag GmbH and Co. KGaA.

Molecular Sequence DataProtein dnaPlasma protein bindingCatalysislaw.inventionCrystalNucleic acid thermodynamicschemistry.chemical_compoundlawNanotechnologyBase sequenceCrystallizationOligonucleotide Array Sequence AnalysisDNA CruciformBase SequenceEscherichia coli ProteinsDNA HelicasesNucleic Acid HybridizationGeneral MedicineDNAGeneral ChemistryDNA-Binding ProteinsMicroscopy ElectronCrystallographychemistryBiochemistryCrystallizationDNAProtein BindingAngewandte Chemie (International ed. in English)
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