Search results for "pair [muon]"

showing 10 items of 18 documents

Prenatal diagnosis of a rhodopsin mutation using chemical cleavage of the mismatch

2002

Objective: Mutations of the rhodopsin gene are responsible for autosomal dominant or recessive retinitis pigmentosa (RP). The present study reports the first prenatal diagnosis performed on chorionic villi biopsy of a pregnant woman affected by a severe form of autosomal dominant transmitted RP, due to the Arg135Trp substitution. Methods: The rhodopsin gene was analysed by automated direct sequencing and, for the first time, by fluorescence-assisted mismatch analysis (FAMA). The latter is an inexpensive, rapid and particularly sensitive method, based on the chemical cleavage of the mismatch in heteroduplex DNA molecules marked with strand-specific fluorophores. Results: FAMA is a feasible p…

AdultRhodopsinrhodopsin geneBase Pair MismatchSettore MED/30 - Malattie Apparato VisivoDNA Mutational Analysisfama; retinitis pigmentosa; rhodopsin geneDNAHeteroduplex AnalysisPolymerase Chain ReactionSettore BIO/18 - GeneticaChorionic Villi SamplingPregnancyretinitis pigmentosaMutationHumansFemalefama
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Quantification of the Detrimental Effect of a Single Primer-Template Mismatch by Real-Time PCR Using the 16S rRNA Gene as an Example

2008

ABSTRACT We investigated the effects of internal primer-template mismatches on the efficiency of PCR amplification using the 16S rRNA gene as the model template DNA. We observed that the presence of a single mismatch in the second half of the primer extension sequence can result in an underestimation of up to 1,000-fold of the gene copy number, depending on the primer and position of the mismatch.

Base Pair MismatchGene DosageBiologyPolymerase Chain ReactionApplied Microbiology and BiotechnologyPrimer extensionlaw.inventionDNA POLYMERASElawRNA Ribosomal 16SMethodsCopy-number variationGenePolymerase chain reactionDNA PrimersADN CIBLE[SDV.EE]Life Sciences [q-bio]/Ecology environmentGeneticsEcologyRibosomal RNA16S ribosomal RNACOPIE DE GENEReal-time polymerase chain reactionPseudomonas aeruginosaPrimer (molecular biology)Food ScienceBiotechnologyApplied and Environmental Microbiology
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Mitochondrial DNA Regionalism and Historical Demography in the Extant Populations of Chirocephalus kerkyrensis (Branchiopoda: Anostraca)

2012

BackgroundMediterranean temporary water bodies are important reservoirs of biodiversity and host a unique assemblage of diapausing aquatic invertebrates. These environments are currently vanishing because of increasing human pressure. Chirocephalus kerkyrensis is a fairy shrimp typical of temporary water bodies in Mediterranean plain forests and has undergone a substantial decline in number of populations in recent years due to habitat loss. We assessed patterns of genetic connectivity and phylogeographic history in the seven extant populations of the species from Albania, Corfu Is. (Greece), Southern and Central Italy.Methodology/principal findingsWe analyzed sequence variation at two mito…

Base Pair MismatchScienceMolecular Sequence DataPopulation DynamicsBiodiversitySettore BIO/05 - ZoologiaPopulation geneticsBranchiopodaMarine and Aquatic SciencesMarine BiologyChirocephalus kerkyrensis Anostraca Phylogeography Mediterranean Temporary PondsExtinction BiologicalDNA MitochondrialHaplogroupGene flowLimnologyAnimalsCluster AnalysisEvolutionary SystematicsBiologyPhylogenyInstitut für Biochemie und BiologieDemographyEvolutionary BiologyMultidisciplinarybiologyEcologyPopulation BiologyEcologyMediterranean RegionQRGenetic VariationPaleontologybiology.organism_classificationPhylogeographyPhylogeographyHabitat destructionHaplotypesAnostracaEarth SciencesMedicineAnostracaZoologyResearch Article
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Nuclear Translocation of Mismatch Repair Proteins MSH2 and MSH6 as a Response of Cells to Alkylating Agents

2000

Mammalian mismatch repair has been implicated in mismatch correction, the prevention of mutagenesis and cancer, and the induction of genotoxicity and apoptosis. Here, we show that treatment of cells specifically with agents inducing O(6)-methylguanine in DNA, such as N-methyl-N'-nitro-N-nitrosoguanidine and N-methyl-N-nitrosourea, elevates the level of MSH2 and MSH6 and increases GT mismatch binding activity in the nucleus. This inducible response occurs immediately after alkylation, is long-lasting and dose-dependent, and results from translocation of the preformed MutSalpha complex (composed of MSH2 and MSH6) from the cytoplasm into the nucleus. It is not caused by an increase in MSH2 gen…

CytoplasmDNA RepairBase Pair MismatchRNA StabilityChromosomal translocationmedicine.disease_causeBiochemistrychemistry.chemical_compoundMismatch Repair Endonuclease PMS2Adenosine TriphosphatasesNuclear ProteinsMethylnitrosoureaNeoplasm ProteinsDNA-Binding ProteinsMutS Homolog 2 ProteinDNA mismatch repairMutL Protein Homolog 1Protein BindingAlkylating AgentsMethylnitronitrosoguanidinecongenital hereditary and neonatal diseases and abnormalitiesGuanineActive Transport Cell NucleusBiologyCell LineO(6)-Methylguanine-DNA MethyltransferaseProto-Oncogene ProteinsDNA Repair ProteinmedicineHumansRNA MessengerneoplasmsMolecular BiologyAdaptor Proteins Signal TransducingCell NucleusMutagenesisnutritional and metabolic diseasesDNACell BiologyDNA MethylationMolecular biologydigestive system diseasesMSH6DNA Repair EnzymesGene Expression RegulationchemistryMSH2Carrier ProteinsGenotoxicityDNADNA DamageHeLa CellsJournal of Biological Chemistry
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Mechanisms and consequences of methylating agent-induced SCEs and chromosomal aberrations: a long road traveled and still a far way to go.

2003

Since the milestone work of Evans and Scott, demonstrating the replication dependence of alkylation-induced aberrations, and Obe and Natarajan, pointing to the critical role of DNA double-strand breaks (DSBs) as the ultimate trigger of aberrations, the field has grown extensively. A notable example is the identification of DNA methylation lesions provoking chromosome breakage (clastogenic) effects, which made it possible to model clastogenic pathways evoked by genotoxins. Experiments with repair-deficient mutants and transgenic cell lines revealed both O<sup>6</sup>-methylguanine (O<sup>6</sup>MeG) and N- methylpurines as critical lesions. For S<sub>N</sub&g…

DNA ReplicationAlkylating AgentsGuanineDNA RepairDNA damageDNA repairBase Pair MismatchApoptosisBiologyMethylationLesionAnimals Genetically ModifiedMiceO(6)-Methylguanine-DNA MethyltransferaseCricetulusCricetinaeGeneticsmedicineAnimalsHumansPoint MutationAP siteMolecular BiologyGenetics (clinical)Chromosome AberrationsRecombination GeneticGuanosineModels GeneticCell CycleDNA replicationDNAFibroblastsMolecular biologyCell killingCell Transformation NeoplasticCancer researchDNA mismatch repairChromosome breakagemedicine.symptomSister Chromatid ExchangeDNA DamageMutagensCytogenetic and genome research
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Common fixed points of generalized contractions on partial metric spaces and an application

2011

Abstract In this paper, common fixed point theorems for four mappings satisfying a generalized nonlinear contraction type condition on partial metric spaces are proved. Presented theorems extend the very recent results of I. Altun, F. Sola and H. Simsek [Generalized contractions on partial metric spaces, Topology and its applications 157 (18) (2010) 2778–2785]. As application, some homotopy results for operators on a set endowed with a partial metric are given.

Discrete mathematicsPartial metric spaceHomotopy.Applied MathematicsInjective metric space010102 general mathematicsEquivalence of metricsCommon fixed point01 natural sciencesCoincidence pointConvex metric spaceIntrinsic metric010101 applied mathematicsComputational MathematicsMetric spaceSettore MAT/05 - Analisi MatematicaMetric (mathematics)Metric mapWeakly compatible pair of mapping0101 mathematicsMetric differentialMathematicsApplied Mathematics and Computation
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Tailoring a pair of pants

2021

Abstract We show how to deform the map Log : ( C ⁎ ) n → R n such that the image of the complex pair of pants P ∘ ⊂ ( C ⁎ ) n is the tropical hyperplane by showing an (ambient) isotopy between P ∘ ⊂ ( C ⁎ ) n and a natural polyhedral subcomplex of the product of the two skeleta S × Σ ⊂ A × C of the amoeba A and the coamoeba C of P ∘ . This lays the groundwork for having the discriminant to be of codimension 2 in topological Strominger-Yau-Zaslow torus fibrations.

General MathematicsImage (category theory)010102 general mathematicsTorusCodimensionMathematics::Geometric Topology01 natural sciencesCombinatoricsMathematics::Algebraic GeometryDiscriminantHyperplane0103 physical sciencesAmoeba (mathematics)Isotopy010307 mathematical physics0101 mathematicsMathematics::Symplectic GeometryPair of pantsMathematicsAdvances in Mathematics
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Mechanisms of human DNA repair: an update.

2003

The human genome, comprising three billion base pairs coding for 30000-40000 genes, is constantly attacked by endogenous reactive metabolites, therapeutic drugs and a plethora of environmental mutagens that impact its integrity. Thus it is obvious that the stability of the genome must be under continuous surveillance. This is accomplished by DNA repair mechanisms, which have evolved to remove or to tolerate pre-cytotoxic, pre-mutagenic and pre-clastogenic DNA lesions in an error-free, or in some cases, error-prone way. Defects in DNA repair give rise to hypersensitivity to DNA-damaging agents, accumulation of mutations in the genome and finally to the development of cancer and various metab…

Genome instabilityGeneticsDNA ReplicationDNA RepairBase pairDNA repairDNA damageBase Pair MismatchDNA replicationDNABiologyToxicologyDNA Repair ProteinAnimalsHumansHuman genomePoly(ADP-ribose) PolymerasesGeneDNA DamageToxicology
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Repair of O(6)-methylguanine is not affected by thymine base pairing and the presence of MMR proteins.

2001

Methylation at the O(6)-position of guanine (O(6)-MeG) by alkylating agents is efficiently removed by O(6)-methylguanine-DNA methyltransferase (MGMT), preventing from cytotoxic, mutagenic, clastogenic and carcinogenic effects of O(6)-MeG-inducing agents. If O(6)-MeG is not removed from DNA prior to replication, thymine will be incorporated instead of cytosine opposite the O(6)-MeG lesion. This mismatch is recognized and processed by mismatch repair (MMR) proteins which are known to be involved in triggering the cytotoxic and genotoxic response of cells upon methylation. In this work we addressed three open questions. (1) Is MGMT able to repair O(6)-MeG mispaired with thymine (O(6)-MeG/T)? (…

GuanineDNA RepairDNA repairGuanineBase Pair MismatchCell SurvivalCHO CellsBiologyToxicologybehavioral disciplines and activitieschemistry.chemical_compoundO(6)-Methylguanine-DNA MethyltransferaseCricetinaeGeneticsCytotoxic T cellAnimalsneoplasmsMolecular BiologyO-6-methylguanine-DNA methyltransferaseMolecular biologydigestive system diseasesThyminenervous systemchemistryDNA mismatch repairpsychological phenomena and processesDNACytosineThymineMutation research
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Modelling of natural and synthetic polyelectrolyte interactions in natural waters.

2006

In this paper SIT and Pitzer models are used for the first time to describe the interactions of natural and synthetic polyelectrolytes in natural waters. Measurements were made potentiometrically at 25 °C in single electrolyte media, such as Et4NI and NaCl (for fulvic acid 0.1 < I /mol L− 1 < 0.75), and in a multi-component medium simulating the composition of natural waters at a wide range of salinities (for fulvic and alginic acids: 5 < S < 45) with particular reference to sea water [Synthetic Sea Water for Equilibrium studies, SSWE]. In order to simplify calculations, SSWE was considered to be a “single salt” BA, with cation B and anion A representing all the major cations (Na+, K+, Mg2+…

Natural and synthetic polyelectrolytes: SITion pair modelDependence on medium and ionic strengthArtificial seawaterdependence on medium and ionic strength: alginic and fulvic acidNatural and synthetic polyelectrolytesSpecific ion Interaction Theory (SIT)PitzerIon Pair modelsAlginic and fulvic acids
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