Search results for "MITOCHONDRIAL DNA"

showing 10 items of 259 documents

Chronic progressive external ophthalmoplegia with a novel mitochondrial DNA deletion and a mutation in the tRNALEU(UUR) gene

1999

Large-scale deletions and point mutations of the mitochondrial DNA are generally accepted as being involved in the pathogenesis of diseases associated with mitochondrial encephalomyopathies such as Kearns-Sayre syndrome and chronic progressive external ophthalmoplegia (CPEO). We screened suspected patients using polymerase chain reaction techniques, Southern blot analyses, and muscle biopsy specimens. We report on a novel 4,953-base pair deletion associated with a familial occurrence of a tRNA Leu(UUR) T3250C point mutation in a young female patient clinically diagnosed with CPEO. This deletion is not flanked by direct repeats, so slip replication and homologous recombination do not seem li…

GeneticsMutationMitochondrial DNAPoint mutationRespiratory chainBiologyMitochondrionmedicine.diseasemedicine.disease_causeHeteroplasmyDrug DiscoverymedicineChronic progressive external ophthalmoplegiaMitochondrial EncephalomyopathiesDrug Development Research
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Mitochondrial DNA mutations in cancer--from bench to bedside.

2009

Mitochondria are cell organelles mostly known for their production of ATP through oxidative phosphorylation. As suggested over 70 years ago by O. Warburg and recently confirmed with molecular techniques, alterations in respiratory activity and mitochondrial DNA appear to be a common feature of malignant cells. Somatic mtDNA mutations have been reported in many types of cancer cells. MtDNA mutation pattern may enhance the specificity of cancer diagnostics, detection and prediction of tumor growth rate and patients' outcome. Therefore it may be used as a molecular cancer bio-marker. Nevertheless recently published papers list a large number of mitochondrial DNA mutations in many different can…

GeneticsMutationMitochondrial DNASettore BIO/16 - Anatomia UmanaSomatic cellRespiratory chainCancerContext (language use)ApoptosisMitochondrionBiologymedicine.disease_causemedicine.diseaseDNA MitochondrialModels BiologicalTranslational Research BiomedicalCell Transformation NeoplasticNeoplasmsCancer cellMutationmedicineHumansCancer Mitochondria Molecular Marker Mutation OXPHOS ReviewReactive Oxygen SpeciesCell ProliferationFrontiers in bioscience (Landmark edition)
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Effect of population structure and migration when investigating genetic continuity using ancient DNA

2016

AbstractRecent advances in sequencing techniques provide means to access direct genetic snapshots from the past with ancient DNA data (aDNA) from diverse periods of human prehistory. Comparing samples taken in the same region but at different time periods may indicate if there is continuity in the peopling history of that area or if a large genetic input, such as an immigration wave, has occurred. Here we propose a new modeling approach for investigating population continuity using aDNA, including two fundamental elements in human evolution that were absent from previous methods: population structure and migration. The method also considers the extensive temporal and geographic heterogeneit…

GeneticsPrehistoryMitochondrial DNAeducation.field_of_studyAncient DNAHuman evolutionEvolutionary biologyPopulation structurePopulationGene poolBiologyeducation
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Genetic differentiation in the striped dolphin Stenella coeruleoalba from European waters according to mitochondrial DNA (mtDNA) restriction analysis

1999

We used mitochondrial DNA (mtDNA) restriction analysis to study genetic variation in 98 striped dolphins (Stenella coeruleoalba) stranded on coasts from different European countries and from animals caught by fisheries. A total of 63 different restriction sites was mapped after digestion of mtDNA with 15 restriction endonucleases that yielded a total of 27 haplotypes. No haplotype was shared between Mediterranean and Atlantic areas. All the analyses indicate the existence of two different populations with a very limited gene flow across the Strait of Gibraltar.

Geneticseducation.field_of_studyMitochondrial DNADolphinsRestriction MappingPopulationGenetic VariationZoologyStenella coeruleoalbaBiologyDNA MitochondrialEuropeRestriction Site PolymorphismRestriction siteRestriction enzymeGenetics PopulationRestriction mapHaplotypesbiology.animalGenetic variationGeneticsAnimalseducationPhylogenyEcology Evolution Behavior and SystematicsMolecular Ecology
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Characterization of a novel open reading frame, urf a, in the mitochondrial genome of fission yeast: correlation of urf a mutations with a mitochondr…

1991

Between the genes for tRNA(gin) and tRNA(ile) an open reading frame of 227 amino acids has been identified which is unique among known mitochondrial genomes and which has been termed urf a (Lang et al. 1983; Kornrumpf et al. 1984). It uses the "mitochondrial" genetic code, i.e., it contains a TGA codon, whereas all other protein-encoding genes, and all but one intronic open reading frame, use the "standard" genetic code (UGG for tryptophan). A previous paper has demonstrated that "mutator" strains show an increased formation of mitochondrial drug-resistant and respiration-deficient mutants (including deletions). In this paper we show that the mutator activity is correlated with mutations in…

GlycerolMitochondrial DNAMutantMolecular Sequence DataExtrachromosomal InheritanceBiologymedicine.disease_causeDNA MitochondrialFrameshift mutationFungal ProteinsMitochondrial ProteinsOpen Reading FramesGene Expression Regulation FungalSchizosaccharomycesGeneticsmedicineAmino Acid SequenceCodonDNA FungalFrameshift MutationGeneGeneticsMutationTranslational frameshiftBase SequenceGeneral MedicineGenetic codeOpen reading framePhenotypeMutationSchizosaccharomyces pombe ProteinsCurrent genetics
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Neolithic mitochondrial haplogroup H genomes and the genetic origins of Europeans

2013

Brotherton, Paul et al.-- The Genographic Consortium

Haplogroup L4aHaplogroup MHaplogroup NTime FactorsHaplogroup HMolecular Sequence DataGeneral Physics and AstronomyADN mitocondrialBiologyGenoma humàGeneral Biochemistry Genetics and Molecular BiologyWhite PeopleArticleEvolution MolecularFilogèniaNeolíticHumansHaplogroup D-M15EuropeusPhylogenyDemographyGeneticsPrincipal Component AnalysisMultidisciplinaryBase SequenceGenome HumanGeneral ChemistryHaplogroup L3Sequence Analysis DNAHaplogroup IJHaplotipGenetics PopulationHaplotypesEvolutionary biologyGenome MitochondrialHuman mitochondrial DNA haplogroupNature Communications
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Meta-Analysis of Mitochondrial DNA Reveals Several Population Bottlenecks during Worldwide Migrations of Cattle

2014

Several studies have investigated the differentiation of mitochondrial DNA in Eurasian, African and American cattle as well as archaeological bovine material. A global survey of these studies shows that haplogroup distributions are more stable in time than in space. All major migrations of cattle have shifted the haplogroup distributions considerably with a reduction of the number of haplogroups and/or an expansion of haplotypes that are rare or absent in the ancestral populations. The most extreme case is the almost exclusive colonization of Africa by the T1 haplogroup, which is rare in Southwest Asian cattle. In contrast, ancient samples invariably show continuity with present-day cattle …

Haplogroup MMitochondrial DNABreedsCATTLEQ1HaplogroupQH301MigrationsBREEDSOtras Ciencias VeterinariasMIGRATIONSlcsh:QH301-705.5Nature and Landscape ConservationHAPLOGROUPSSettore AGR/17 - ZOOTECNICA GENERALE E MIGLIORAMENTO GENETICOEcologybiologyEcologyCiencias VeterinariasEcological ModelingHaplotypeHaplogroup L3biology.organism_classificationAgricultural and Biological Sciences (miscellaneous)Mitochondrial DNAhumanitiesMitochondrialEcological ModellingPopulation bottlenecklcsh:Biology (General)CIENCIAS AGRÍCOLASAmerican cattleEvolutionary biologyHaplogroupsCattleMITOCHONDRIAL DNA//purl.org/becyt/ford/4.3 [https]//purl.org/becyt/ford/4 [https]Meta-AnalysisHuman mitochondrial DNA haplogroupDiversity
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Population structure and mitochondrial DNA gene flow in Old World populations of Drosophila subobscura

1992

An extensive survey of mitochondrial DNA (mtDNA) restriction polymorphism in 156 isofemale lines from 29 different geographic populations of Drosophila subobscura distributed throughout the Old World was carried out. Ten restriction enzymes were used, five of which revealed restriction site polymorphism. Of the 31 restriction sites detected, 13 were found to be polymorphic. Comparisons with the mtDNA map of Drosophila yakuba indicate that the variable sites are mainly concentrated in protein genes, especially those corresponding to the NADH complex. A total of 13 different haplotypes were observed, two of which (haplotypes I and II) are quite frequent and widely distributed throughout the p…

HeterozygoteMitochondrial DNAPopulationPopulation geneticsDNA MitochondrialGene FrequencyGeneticsAnimalseducationAllelesGenetics (clinical)Geneticseducation.field_of_studybiologybiology.organism_classificationDrosophila subobscuraIsoenzymesRestriction Site PolymorphismRestriction siteGenetics PopulationHaplotypesDrosophilaFemaleRestriction fragment length polymorphismPolymorphism Restriction Fragment LengthDrosophila yakubaHeredity
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Linkage disequilibria between mtDNA haplotypes and chromosomal arrangements in a natural population of Drosophila subobscura

2001

The association between mtDNA haplotypes and chromosomal arrangements in a natural population of Drosophila subobscura from Calvia (Balearic Islands, Spain) was studied in order to search for linkage disequilibria, in an attempt to explain the populational dynamics of the mtDNA haplotypes of this species in nature. The presence of Wolbachia was not detected. Two main haplotypes (I and II) were found, as well as a series of less common ones. The Tajima D-test seemed to indicate some kind of seasonal population bottleneck. An analysis of linkage disequilibrium and factorial analysis of correspondences detected an association between haplotype I and the J(ST) inversion and haplotype II and the…

Linkage (software)GeneticsLinkage disequilibriumMitochondrial DNAHaplotypeBiologybiology.organism_classificationDNA MitochondrialLinkage DisequilibriumDrosophila subobscuraGenetics PopulationPopulation bottleneckHaplotypesNatural population growthGeneticsAnimalsDrosophilaWolbachiaGenetics (clinical)Heredity
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Mitochondrial oxidative injury: a key player in nonalcoholic fatty liver disease.

2020

Nonalcoholic fatty liver disease (NAFLD) has become the most prevalent liver disease worldwide. NAFLD is tightly linked to the metabolic syndrome, insulin resistance, and oxidative stress. Globally, its inflammatory form, nonalcoholic steatohepatitis (NASH), has become the main cause of liver-related morbidity and mortality, mainly due to liver cirrhosis and primary liver cancer. One hallmark of NASH is the presence of changes in mitochondrial morphology and function that are accompanied by a blocked flow of electrons in the respiratory chain, which increases formation of mitochondrial reactive oxygen species in a self-perpetuating vicious cycle. Consequences are oxidation of DNA bases and …

Liver Cirrhosismedicine.medical_specialtyMitochondrial DNAMitochondrial DiseasesPhysiologyMitochondrial TurnoverRespiratory chainBiologymedicine.disease_causedigestive system03 medical and health sciences0302 clinical medicineNon-alcoholic Fatty Liver DiseasePhysiology (medical)Internal medicineMitochondrial unfolded protein responseMitophagyNonalcoholic fatty liver diseasemedicineAnimalsHumans030304 developmental biology0303 health sciencesHepatologyGastroenterologynutritional and metabolic diseasesmedicine.diseasedigestive system diseases3. Good healthFatty LiverOxidative StressEndocrinologyMitochondrial biogenesis030211 gastroenterology & hepatologyOxidative stressAmerican journal of physiology. Gastrointestinal and liver physiology
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