Search results for " Common"

showing 10 items of 343 documents

Reconstructing the ancestor of Mycobacterium leprae: The dynamics of gene loss and genome reduction

2007

We have reconstructed the gene content and order of the last common ancestor of the human pathogens Mycobacterium leprae and Mycobacterium tuberculosis. During the reductive evolution of M. leprae, 1537 of 2977 ancestral genes were lost, among which we found 177 previously unnoticed pseudogenes. We find evidence that a massive gene inactivation took place very recently in the M. leprae lineage, leading to the loss of hundreds of ancestral genes. A large proportion of their nucleotide content (∼89%) still remains in the genome, which allowed us to characterize and date them. The age of the pseudogenes was computed using a new methodology based on the rates and patterns of substitution in the…

Most recent common ancestorGeneticsLetterLineage (genetic)PseudogeneComputational BiologyMycobacterium tuberculosisBiologybiology.organism_classificationGenomeEvolution MolecularMycobacterium lepraeMycobacterium tuberculosisPhylogeneticsGeneticsDNA FungalMycobacterium lepraeGeneGene DeletionGenome BacterialPhylogenyGenetics (clinical)Genome Research
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Evolution of arginine deiminase (ADI) pathway genes

2002

We have analyzed the evolution of the three genes encoding structural enzymes of the arginine deiminase (ADI) pathway, arginine deiminase (ADI), ornithine transcarbamoylase (OTC), and carbamate kinase (CK) in a wide range of organisms, including Archaea, Bacteria, and Eukarya. This catabolic route was probably present in the last common ancestor to all the domains of life. The results obtained indicate that these genes have undergone a complex evolutionary history, including horizontal transfer events, duplications, and losses. Therefore, these genes are not adequate to infer organismal relationships at deep branching levels, but they provide an insight into how catabolic genes evolved and …

Most recent common ancestorHydrolasesMolecular Sequence DataBiologyModels BiologicalEvolution MolecularGeneticsAmino Acid SequenceMolecular BiologyArginine deiminase pathwayGeneArginine deiminaseOrnithine CarbamoyltransferasePhylogenyEcology Evolution Behavior and SystematicsGeneticsLikelihood FunctionsBacteriaSequence Homology Amino AcidPhylogenetic treeCarbamate kinaseFungiSequence Analysis DNAPhosphotransferases (Carboxyl Group Acceptor)ArchaeaMetabolic pathwayHorizontal gene transferMolecular Phylogenetics and Evolution
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Ligand Diversity of Human and Chimpanzee CYP3A4: Activation of Human CYP3A4 by Lithocholic Acid Results from Positive SelectionS⃞

2009

For currently unknown reasons, the evolution of CYP3A4 underwent acceleration in the human lineage after the split from chimpanzee. We investigated the significance of this event by comparing Escherichia coli-expressed CYP3A4 from humans, chimpanzee, and their most recent common ancestor. The expression level of chimpanzee CYP3A4 was ∼50% of the human CYP3A4, whereas ancestral CYP3A4 did not express in E. coli. Steady-state kinetic analysis with 7-benzyloxyquinoline, 7-benzyloxy-4-(trifluoromethyl)coumarin (7-BFC), and testosterone showed no significant differences between human and chimpanzee CYP3A4. Upon addition of α-naphthoflavone (25 μM), human CYP3A4 showed a slightly decreased substr…

Most recent common ancestorModels MolecularLithocholic acidLineage (genetic)Pan troglodytesmedicine.drug_classPharmaceutical ScienceLigandsIsozymechemistry.chemical_compoundSpecies SpecificityCoumarinsmedicineAnimalsCytochrome P-450 CYP3AHumansPharmacologychemistry.chemical_classificationBinding SitesbiologyBile acidCYP3A4Cytochrome P450ArticlesAmino acidEnzyme ActivationchemistryBiochemistrybiology.proteinLithocholic AcidSteroids
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Analysis of DNA sequence variation within marine species using Beta-coalescents

2013

We apply recently developed inference methods based on general coalescent processes to DNA sequence data obtained from various marine species. Several of these species are believed to exhibit so-called shallow gene genealogies, potentially due to extreme reproductive behaviour, e.g. via Hedgecock's "reproduction sweepstakes". Besides the data analysis, in particular the inference of mutation rates and the estimation of the (real) time to the most recent common ancestor, we briefly address the question whether the genealogies might be adequately described by so-called Beta coalescents (as opposed to Kingman's coalescent), allowing multiple mergers of genealogies. The choice of the underlying…

Most recent common ancestorMutation ratePopulation geneticsInferenceMarine Biology62F99 (Primary) 62P10 92D10 92D20 (Secondary)Biology01 natural sciencesArticleDNA sequencingCoalescent theory010104 statistics & probability03 medical and health sciencesFOS: MathematicsAnimals0101 mathematicsQuantitative Biology - Populations and EvolutionEcology Evolution Behavior and Systematics030304 developmental biologycomputer.programming_languageMarine biology0303 health sciencesBETA (programming language)Probability (math.PR)Populations and Evolution (q-bio.PE)Sequence Analysis DNAOstreidaeEvolutionary biologyFOS: Biological sciencescomputerMathematics - Probability
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2021

Studies on the function of PRDM9 in model systems and its evolution during vertebrate divergence shed light on the basic molecular mechanisms of hybrid sterility and its evolutionary consequences. However, information regarding PRDM9-homolog, PRDM7, whose origin is placed in the primate evolutionary tree, as well as information about the fast-evolving DNA-binding zinc finger array of strepsirrhine PRDM9 are scarce. Thus, we aimed to narrow down the date of the duplication event leading to the emergence of PRDM7 during primate evolution by comparing the phylogenetic tree reconstructions of representative primate samples of PRDM orthologs and paralogs. To confirm our PRDM7 paralogization patt…

Most recent common ancestorZinc finger0303 health sciencesPapioniniPhylogenetic treebiologybiology.organism_classificationTarsier03 medical and health sciences0302 clinical medicinePhylogeneticsEvolutionary biologyGene duplicationGeneticsMolecular Medicine030217 neurology & neurosurgeryGenetics (clinical)PRDM9030304 developmental biologyFrontiers in Genetics
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Whole mitochondrial genomes unveil the impact of domestication on goat matrilineal variability

2015

Background The current extensive use of the domestic goat (Capra hircus) is the result of its medium size and high adaptability as multiple breeds. The extent to which its genetic variability was influenced by early domestication practices is largely unknown. A common standard by which to analyze maternally-inherited variability of livestock species is through complete sequencing of the entire mitogenome (mitochondrial DNA, mtDNA). Results We present the first extensive survey of goat mitogenomic variability based on 84 complete sequences selected from an initial collection of 758 samples that represent 60 different breeds of C. hircus, as well as its wild sister species, bezoar (Capra aega…

Most recent common ancestor[SDV]Life Sciences [q-bio]PopulationMolecular Sequence DataMtDNA haplogroupsCapra aegagrusBiologyDNA MitochondrialHaplogroupDomesticationQH301Settore AGR/17 - Zootecnica Generale E Miglioramento GeneticoCapra hircusGeneticsAnimalsCapra aegagruDomesticationeducationQH426Phylogeny2. Zero hungereducation.field_of_studyOrigin of Capra hircusGenomeMtDNA haplogroupPhylogenetic treeGoatsHaplotypeGenetic VariationDNAOrigin of Capra hircuMitochondrialCapra aegagrus; Domestication; Goat mitochondrial genome; MtDNA haplogroups; Origin of Capra hircus; Biotechnology; GeneticsHaplotypesEvolutionary biologyGoat mitochondrial genomeGenome MitochondrialCapra aegagrus; Domestication; Goat mitochondrial genome; MtDNA haplogroups; Origin of Capra hircus; Animals; DNA Mitochondrial; Female; Genetic Variation; Genome Mitochondrial; Goats; Haplotypes; Molecular Sequence Data; Phylogeny; Biotechnology; GeneticsmtDNA haplogroupsFemaleResearch ArticleHuman mitochondrial DNA haplogroupBiotechnology
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Pre- and post-ictal brain activity characterization using combined source decomposition and connectivity estimation in epileptic children

2019

In this research, the study of functional connectivity between sources of electroencephalogram (EEG) activity assessed for different classes (well before seizure, preictal and post-ictal) was performed. EEG recordings were acquired from 12 subjects with focal epilepsy. Then, ten common spatial patterns (CSP) were obtained for EEG segments describing 95% of Riemannian distance between pairs of classes, followed by estimation of multivariate autoregressive (MVAR) models’ coefficients. The MVAR models were further used to extract coherence as a functional connectivity measures. Our results show that the coherence between CSP sources differs between baseline and pre-ictal segments: it has the l…

Multivariate statisticsepilepsy epileptic seizures EEG brain connectivity common spatial patterns VAR model ICAmedicine.diagnostic_testComputer sciencebusiness.industryBrain activity and meditationPattern recognitionCoherence (statistics)Electroencephalographymedicine.diseaseSettore ING-INF/01 - ElettronicaEpilepsyAutoregressive modelSettore ING-INF/06 - Bioingegneria Elettronica E InformaticamedicineIctalArtificial intelligencebusinessPre and post
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The Role of Erythropoietin in Neuroprotection: Therapeutic Perspectives

2007

Nervous system diseases are very complex conditions comprising a large variety of local and systemic responses. Several therapeutic agents interfering with all or in part the biochemical steps that ultimately cause neuronal death have been demonstrated to be neuroprotective in preclinical models. However, all the agents so far investigated have inexorably failed in the phase III trials carried out. A large body of evidence suggests that the hormone erythropoietin (EPO), besides its well-known hematopoietic action, exerts beneficial effects in the central nervous system. EPO's effect has been assessed in several experimental models of brain and spinal cord injury thus becoming a serious cand…

Nervous systemEXPERIMENTAL SUBARACHNOID HEMORRHAGECentral nervous systemSIGNAL-TRANSDUCTIONPharmacologyModels BiologicalNeuroprotectionErythropoietin in neuroprotectionNEURONAL APOPTOSISCEREBROSPINAL-FLUIDAnimalsHumansMedicineIN-VIVO EVIDENCEErythropoietinSpinal cord injuryPharmacologyCEREBRAL-ISCHEMIACOMMON BETA-SUBUNITbusiness.industryRECOMBINANT-HUMAN-ERYTHROPOIETIN; GLYCOGEN-SYNTHASE KINASE-3-BETA; EXPERIMENTAL SUBARACHNOID HEMORRHAGE; COMMON BETA-SUBUNIT; IN-VIVO EVIDENCE; CEREBRAL-ISCHEMIA; SIGNAL-TRANSDUCTION; CEREBROSPINAL-FLUID; NEURONAL APOPTOSIS; CYTOKINE RECEPTORSRECOMBINANT-HUMAN-ERYTHROPOIETINmedicine.diseaseRecombinant ProteinsEnzyme ActivationStrokeClinical trialNeuroprotective AgentsTreatment Outcomemedicine.anatomical_structureErythropoietinGLYCOGEN-SYNTHASE KINASE-3-BETACYTOKINE RECEPTORSBone marrowMitogen-Activated Protein Kinasesbusinessmedicine.drugDrug News & Perspectives
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Pediatric neurofibromatosis 1 and parental stress: a multicenter study

2014

Maria Esposito,1 Rosa Marotta,2 Michele Roccella,3 Beatrice Gallai,4 Lucia Parisi,3 Serena Marianna Lavano,2 Marco Carotenuto1 1Clinic of Child and Adolescent Neuropsychiatry, Department of Mental Health, Physical and Preventive Medicine, Second University of Naples, Naples, Italy; 2Department of Psychiatry, "Magna Graecia" University of Catanzaro, Catanzaro, Italy; 3Child Neuropsychiatry, Department of Psychology, University of Palermo, Palermo, Italy; 4Unit of Child and Adolescent Neuropsychiatry, University of Perugia, Perugia, Italy Background: Neurofibromatosis 1 (NF1) is a complex and multifaceted neurocutaneous syndrome with many and varied comorbidities. The litera…

Neuropsychiatric Disease and TreatmentNon commercialOperations researchComputer scienceShort ReportLibrary scienceCreative commonslcsh:RC346-429Settore MED/39 - Neuropsichiatria Infantilelcsh:RC321-571Psychiatry and Mental healthMaternal stressMulticenter studychildrenmaternal stressvon Recklingausen diseaseParental stressParental Stress IndexLicenselcsh:Neurosciences. Biological psychiatry. NeuropsychiatryBiological PsychiatryDovelcsh:Neurology. Diseases of the nervous system
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NA48/62 latest results

2017

The NA62 experiment at the CERN SPS recorded in 2007 a large sample of K+ ? µ+?µ decays. A peak search in the missing mass spectrum of this decay is performed. In the absence of observed signal, the limits obtained on B(K+ ? µ+?h) and on the mixing matrix element |Uµ 4| are reported. The upgraded NA62 experiment started data taking in 2015. About 5×1011K+ decays have been recorded so far to measure the branching ratio of the K+ ? ?+?? decay. Preliminary results from the K+ ? ?+?? analysis based on about 5% of the 2016 statistics are reported.

Nuclear physicsPhysicsParticle physicsBranching fractionTheoryofComputation_ANALYSISOFALGORITHMSANDPROBLEMCOMPLEXITYMass spectrumMatrix elementCreative commonsNA62 experimentParticle Physics - ExperimentSettore FIS/04 - Fisica Nucleare e SubnucleareLarge sample
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