Search results for "Gene Expression"

showing 10 items of 4085 documents

Isolation and characterization of five Fox (Forkhead) genes from the sponge Suberites domuncula.

2003

Fox or Forkhead genes constitute a subgroup of the helix-turn-helix class of transcription factors with a characteristic and highly conserved DNA binding domain. To date, around 100 different Fox genes have been reported ranging from yeast to humans; these have been classified into 18 subclasses (A to P). Fox proteins are responsible for a wide range of functions and key roles in early developmental processes, during organogenesis and also for the function of the major organs and tissues in the adult. Here, we report the isolation and phylogenetic characterization of five members of the Fox family from the sponge Suberites domuncula. Four of them (Sd-FoxL2, Sd-FoxP, Sd-FoxD and Sd-FoxF) fal…

DNA ComplementaryTime FactorsSequence analysisMolecular Sequence DataSequence alignmentBiologyFOX proteinsPhylogeneticsparasitic diseasesGeneticsAnimalsCloning MolecularGeneCells CulturedPhylogenyGeneticsSequence Homology Amino AcidGene Expression ProfilingGeneral MedicineDNA-binding domainAnatomySequence Analysis DNAbiology.organism_classificationPoriferaSuberites domunculaSpongeMultigene FamilySequence AlignmentTranscription FactorsGene
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Expression profiling of uniparental mouse embryos is inefficient in identifying novel imprinted genes

2006

AbstractImprinted genes are expressed from only one allele in a parent-of-origin-specific manner. We here describe a systematic approach to identify novel imprinted genes using quantification of allele-specific expression by Pyrosequencing, a highly accurate method to detect allele-specific expression differences. Sixty-eight candidate imprinted transcripts mapping to known imprinted chromosomal regions were selected from a recent expression profiling study of uniparental mouse embryos and analyzed. Three novel imprinted transcripts encoding putative non-protein-coding RNAs were identified on the basis of parent-of-origin-specific monoallelic expression in E11.5 (C57BL/6 × Cast/Ei)F1 and in…

DNA ComplementaryTranscription GeneticGenomic imprintingMouseParthenogenesisGene ExpressionGenomicsMice Inbred StrainsUniparental embryoBiologyPolymorphism Single NucleotideChromosomesMicePregnancyDatabases GeneticGeneticsAnimalsRNA MessengerAlleleGeneAllelesCrosses GeneticGeneticsModels GeneticChromosome MappingGenetic VariationPyrosequencingEmbryoParthenogenesisDNAEmbryo MammalianGene expression profilingGene expression profilingMice Inbred C57BLPyrosequencingRNAFemaleGenomic imprintingPrader-Willi SyndromeSoftwareGenomics
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Molecular cloning of rat G-protein-coupled receptor kinase 6 (GRK6) from brain tissue, and its mRNA expression in different brain regions and periphe…

1997

The rat G-protein-coupled receptor kinase 6 (GRK6) cDNA was cloned from rat brain tissue by a combination of reverse-transcription polymerase chain reactions (RT-PCR), based on homology to the cloned human GRK6, and rapid amplification of cDNA ends (RACE-PCR). We obtained a clone of 2817 bp with an open reading frame of 1731 bp encoding for a protein of 576 amino acids that is 96.7% identical and 97.9% similar to its human counterpart. mRNA was detectable in all brain areas examined. In addition, GRK6 was expressed in skeletal muscle, small intestine, aorta, liver, heart, lung, thymus, stomach, uterus and kidney.

DNA ComplementaryTranscription GeneticMolecular Sequence DataProtein Serine-Threonine KinasesMolecular cloningBiologyPolymerase Chain ReactionOpen Reading FramesCellular and Molecular NeuroscienceRapid amplification of cDNA endsGTP-Binding ProteinsComplementary DNAGene expressionAnimalsHumansAmino Acid SequenceRNA MessengerCloning MolecularProtein kinase AMolecular BiologyG protein-coupled receptor kinaseMessenger RNABase SequenceSequence Homology Amino AcidBrainReceptor Protein-Tyrosine KinasesG-Protein-Coupled Receptor KinasesMolecular biologyRatsOpen reading frameOrgan SpecificityFemaleSequence AlignmentMolecular Brain Research
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Cloning, structure, cellular localization, and possible function of the tumor suppressor gene lethal(3)malignant blood neoplasm-1 of Drosophila melan…

1994

The tumor suppressor gene, lethal(3)malignant blood neoplasm-1+, of Drosophila melanogaster is required for the differentiation of the phagocytic blood-cell type, the plasmatocyte. In the homozygously mutated state it causes the malignant transformation of these blood cells. We present here the cloning, sequencing, structure, and expression of the l(3)mbn-1+ gene during development. The cloned gene was identified by germ-line transformation, generation of revertants, and the detection of the corresponding mRNA in blood cells and other tissues. Homologies of the G-S-rich C-terminus of the putative MBN83 protein to human cytokeratins K1, K10, and mouse loricrin were found. The structure and p…

DNA ComplementaryTumor suppressor geneMolecular Sequence DataMalignant transformationGene expressionAnimalsGenes Tumor SuppressorAmino Acid SequenceRNA MessengerCloning MolecularMolecular BiologyGeneCellular localizationAllelesCloningBlood CellsbiologyBase SequenceChromosome MappingCell Biologybiology.organism_classificationMolecular biologyCell Transformation NeoplasticDrosophila melanogasterLoricrinDrosophila melanogasterDevelopmental BiologyDevelopmental biology
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Homeobox-containing gene transiently expressed in a spatially restricted pattern in the early sea urchin embryo

1995

In the sea urchin embryo, the lineage founder cells whose polyclonal progenies will give rise to five different territories are segregated at the sixth division. To investigate the mechanisms by which the fates of embryonic cells are first established, we looked for temporal and spatial expression of homeobox genes in the very early cleavage embryos. We report evidence that PlHbox12, a paired homeobox-containing gene, is expressed in the embryo from the 4-cell stage. The abundance of the transcripts reaches its maximum when the embryo has been divided into the five polyclonal territories--namely at the 64-cell stage--and it abruptly declines at later stages of development. Blastomere dissoc…

DNA Complementaryanimal structuresLineage (genetic)Molecular Sequence DataSettore BIO/11 - Biologia MolecolareIn situ hybridizationBiologysea urchinAnimalsAmino Acid SequenceGeneRegulation of gene expressionMultidisciplinaryBase SequenceSequence Homology Amino AcidhomeoboxGenes HomeoboxGene Expression Regulation DevelopmentalEmbryoBlastomereMolecular biologyEmbryonic stem cellSea Urchinsembryonic structuresHomeoboxResearch Article
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Cloning and Sequencing of a cDNA Encoding a Larval-Pupal-Specific Cuticular Protein in Tenebrio Molitor (Insecta, Coleoptera). Developmental Expressi…

1996

A cDNA clone encoding a larval-pupal cuticular protein, named TMLPCP-22, has been isolated by screening a library in expression vector with a monoclonal antibody made against pupal cuticular proteins of Tenebrio molitor. Northern-blot and in situ hybridization analyses showed that the expression of TMLPCP-22 is regulated in a stage-specific and tissue-specific manner; the transcript was present during the secretion of preecdysial larval and pupal cuticles and was restricted to epidermal cells. No expression was observed during adult cuticle deposition. In supernumerary pupae obtained after application of a juvenile hormone analogue, which is known to inhibit the adult programme, TMLPCP-22 m…

DNA Complementaryanimal structuresmedia_common.quotation_subjectCuticleMolecular Sequence DataGenes InsectIn situ hybridizationBiologyBiochemistryComplementary DNAGene expressionAnimalsAmino Acid SequenceRNA MessengerCloning MolecularMetamorphosisTenebrioIn Situ HybridizationDNA Primersmedia_commonCloningExpression vectorBase SequenceSequence Homology Amino AcidfungiMetamorphosis BiologicalPupaGene Expression Regulation DevelopmentalProteinsMolecular biologyJuvenile HormonesLarvaJuvenile hormoneEuropean Journal of Biochemistry
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Metatranscriptomic Approach to Analyze the Functional Human Gut Microbiota

2011

The human gut is the natural habitat for a large and dynamic bacterial community that has a great relevance for health. Metagenomics is increasing our knowledge of gene content as well as of functional and genetic variability in this microbiome. However, little is known about the active bacteria and their function(s) in the gastrointestinal tract. We performed a metatranscriptomic study on ten healthy volunteers to elucidate the active members of the gut microbiome and their functionality under conditions of health. First, the microbial cDNAs obtained from each sample were sequenced using 454 technology. The analysis of 16S transcripts showed the phylogenetic structure of the active microbi…

DNA Complementarylcsh:MedicineGastroenterology and HepatologyGut floraPrevotellaceaeMicrobiologyMicrobiologyMicrobial EcologyMicrobial PhysiologyRNA Ribosomal 16SHumansMicrobiomeRNA Messengerlcsh:ScienceGeneBacteroidaceaeBiologyGeneticsMultidisciplinarybiologyBacteriaGene Expression ProfilingLachnospiraceaelcsh:RComputational BiologyGenomicsBiodiversitySequence Analysis DNAbiology.organism_classificationGastrointestinal TractMetagenomicsMedicineSmall IntestineMetagenomelcsh:QMetagenomicsGenome Expression AnalysisRuminococcaceaeResearch ArticlePLoS ONE
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The Implication of Xyloglucan Endotransglucosylase/Hydrolase (XTHs) in Tomato Fruit Infection by Penicillium expansum Link. A

2007

In general, cell wall-degrading enzymes produced by plant pathogenic fungi are considered important pathogenicity factors. In this work, we evaluate the implication of xyloglucan endotransglucosylase/ hydrolase (XTHs), a potential hemicellulosic repairing enzyme, in the infection mechanism process by the fungus. This study investigated the SIXTHS expresion and xyloglucan endotransglucosylase (XET) activity during infection of two tomato fruit cultivars by Penicillium expansum Link. A. In infected fruits, XET specific activity decreased drastically after long infection periods, 24 and 48 h for Canario and Money Maker tomato fruits, respectively. Real Time RT-PCR of eleven SIXTHS also showed …

DNA PlantArabidopsisGene ExpressionFungusMicrobiologyCell wallchemistry.chemical_compoundSolanum lycopersicumLegumePlant DiseasesbiologyfungiPenicilliumGlycosyltransferasesfood and beveragesGeneral ChemistryFungi imperfectiXyloglucan endotransglucosylasebiology.organism_classificationXyloglucanchemistryBiochemistryFruitPenicillium expansumGeneral Agricultural and Biological SciencesSequence AlignmentSolanaceaeJournal of Agricultural and Food Chemistry
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Computational annotation of genes differentially expressed along olive fruit development

2009

Abstract Background Olea europaea L. is a traditional tree crop of the Mediterranean basin with a worldwide economical high impact. Differently from other fruit tree species, little is known about the physiological and molecular basis of the olive fruit development and a few sequences of genes and gene products are available for olive in public databases. This study deals with the identification of large sets of differentially expressed genes in developing olive fruits and the subsequent computational annotation by means of different software. Results mRNA from fruits of the cv. Leccino sampled at three different stages [i.e., initial fruit set (stage 1), completed pit hardening (stage 2) a…

DNA PlantBERRY DEVELOPMENTGenomicsComputational biologyPlant ScienceBiologyGenes PlantGenomeGene Expression Regulation PlantOlealcsh:BotanyBotanyCluster AnalysisFUNCTIONAL GENOMICSGene Regulatory NetworksKEGGBlast2GOGene LibraryExpressed sequence tagGene Expression ProfilingComputational BiologySequence Analysis DNAGRAPE BERRIESREDUCTASE GENEEST DATABASEOLEA-EUROPAEAlcsh:QK1-989Gene expression profilingOLEA-EUROPAEA; SEQUENCE TAGS; TRANSIENT EXPRESSION; FUNCTIONAL GENOMICS; BERRY DEVELOPMENT; POTENTIAL ROLES; DESATURASE GENE; REDUCTASE GENE; GRAPE BERRIES; EST DATABASESuppression subtractive hybridizationFruitPOTENTIAL ROLESDESATURASE GENETRANSIENT EXPRESSIONFunctional genomicsMetabolic Networks and PathwaysSEQUENCE TAGSResearch ArticleBMC Plant Biology
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Development-dependent changes in the tight DNA-protein complexes of barley on chromosome and gene level

2008

Abstract Background The tightly bound to DNA proteins (TBPs) is a protein group that remains attached to DNA with covalent or non-covalent bonds after its deproteinisation. The functional role of this group is as yet not completely understood. The main goal of this study was to evaluate tissue specific changes in the TBP distribution in barley genes and chromosomes in different phases of shoot and seed development. We have: 1. investigated the TBP distribution along Amy32b and Bmy1 genes encoding low pI α-amylase A and endosperm specific β-amylase correspondingly using oligonucleotide DNA arrays; 2. characterized the polypeptide spectrum of TBP and proteins with affinity to TBP-associated D…

DNA PlantTranscription GeneticPlant ScienceBiologyGenes PlantChromosomes Plantchemistry.chemical_compoundGene Expression Regulation Plantlcsh:BotanyGene expressionPromoter Regions GeneticGeneOligonucleotide Array Sequence AnalysisPlant ProteinsOligonucleotideIntronGene Expression Regulation Developmentalfood and beveragesChromosomeHordeumPromoterExonsNuclear matrixMolecular biologyIntronslcsh:QK1-989DNA-Binding ProteinschemistryBiochemistrySeedsPlant ShootsDNAMicrosatellite RepeatsResearch ArticleBMC Plant Biology
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