Search results for "sequences"

showing 10 items of 359 documents

Mitochondrial DNA sequence data support the allocation of Greek mainland chameleons to Chamaeleo africanus

1999

Arnold, E.N., Burton, J.A. (1978): Reptiles and Amphibians of Britain and Europe. London, Collins & Sons.Bruno, S., Maugeri, S. (1990): Guida ai serpenti d’ Italia e d’ Europa. Milano, Editoriale Giorgio Mondadori.Carpenter, C.C., Ferguson, G.W. (1977): Variation and evolution of stereotyped behaviour in reptiles. In: Biologyof theReptilia, Vol. 7, p. 335-554. Gans, C., Tinkle, D.W.,Eds, London, New York, San Francisco, AcademicPress.Tomaselli, R., Balduzzi, A., Filipello, S. (1973): Carta Bioclimatica d’ Italia. Collana Verde 33, MinisteroAgricoltura eForeste, Roma.

Mitochondrial DNAData sequencesEcologyStereotyped behaviourAnimal Science and ZoologyMainlandChamaeleoBiologybiology.organism_classificationEcology Evolution Behavior and SystematicsAmphibia-Reptilia
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Mitochondrial genome of Suberites domuncula: palindromes and inverted repeats are abundant in non-coding regions.

2007

The 26,300-nucleotide sequence of the mitochondrial DNA (mtDNA) molecule of the demosponge Suberites domuncula (Olivi, 1792), the largest in size yet found in Porifera, has been determined. We describe the second hadromerid sponge mitochondrial genome that contains the same set of 41 genes as the hadromerid sponge Tethya actinia, including trnMe(cau), trnI2(cau), trnR2(ucu), and atp9, all of which are transcribed in the same direction. Furthermore, rRNA genes for the small and large ribosomal subunit are very long, rns is indeed the longest among Metazoa (1833 bp). Intergenic regions (IGR) comprise about 25% of S. domuncula mtDNA and include numerous direct and inverted repeats, as well as …

Mitochondrial DNAInverted repeatMolecular Sequence DataSuberites ficusDNA MitochondrialIntergenic regionRNA TransferSpecies SpecificityLarge ribosomal subunitSequence Homology Nucleic AcidGeneticsAnimalsGenePhylogenyRepetitive Sequences Nucleic AcidGeneticsPorifera ; Hadromerida ; mtDNA ; mitochondrial evolution ; polymorphismsBase CompositionbiologyBase SequenceGenetic VariationGeneral MedicineRibosomal RNAbiology.organism_classificationSuberites domunculaGenome MitochondrialDNA IntergenicSuberitesGene
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Role of RNA Guanine Quadruplexes in Favoring the Dimerization of SARS Unique Domain in Coronaviruses

2020

ABSTRACTCoronaviruses may produce severe acute respiratory syndrome (SARS). As a matter of fact, a new SARS-type virus, SARS-CoV-2, is responsible of a global pandemic in 2020 with unprecedented sanitary and economic consequences for most countries. In the present contribution we study, by all-atom equilibrium and enhanced sampling molecular dynamics simulations, the interaction between the SARS Unique Domain and RNA guanine quadruplexes, a process involved in eluding the defensive response of the host thus favoring viral infection of human cells. Our results evidence two stable binding modes involving an interaction site spanning either the protein dimer interface or only one monomer. The …

Models Molecular0301 basic medicineLetterSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2)DimerPneumonia ViralCoronaviruProtein dimerMolecular Dynamics SimulationViral infection01 natural sciencesVirusBetacoronavirus03 medical and health scienceschemistry.chemical_compound0302 clinical medicine0103 physical sciencesG-QuadruplexeHumans[CHIM]Chemical SciencesGeneral Materials Science030212 general & internal medicinePhysical and Theoretical ChemistryPandemicsEconomic consequences030304 developmental biology0303 health sciences010304 chemical physicsBetacoronaviruSARS-CoV-2ChemistryCoronavirus InfectionRational designCOVID-19RNASpike Glycoprotein3. Good healthG-Quadruplexes030104 developmental biologySettore CHIM/03 - Chimica Generale E InorganicaSpike Glycoprotein CoronavirusBiophysicsRNA ViralCoronavirus InfectionsGuanine-QuadruplexesDimerizationProtein Binding
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Complex evolution of tandem-repetitive DNA in the Chironomus thummi species group.

1997

The subspecies Chironomus thummi thummi and C. t. piger display dramatic differences in the copy number and chromosomal localization of a tandemly repeated DNA family (Cla elements). In order to analyze the evolutionary dynamics of this repeat family, we studied the organization of Cla elements in the related outgroup species C. luridus. We find three different patterns of Cla element organization in C. luridus, showing that Cla elements may be either strictly tandem-repetitive or be an integral part of two higher-order tandem repeats (i.e., Hinf[lur] elements, Sal[lur] elements). All three types of Cla-related repeats are localized in the centromeres of C. luridus chromosomes. This suggest…

Molecular Sequence DataBiologySubspeciesChironomidaeTransposition (music)Evolution Molecularchemistry.chemical_compoundTandem repeatSpecies SpecificityCentromereGeneticsAnimalsCloning MolecularRepeated sequenceMolecular BiologyEcology Evolution Behavior and SystematicsIn Situ HybridizationRepetitive Sequences Nucleic AcidCloningGeneticsintegumentary systemBase Sequencefood and beveragesDNAchemistryNucleic acidlipids (amino acids peptides and proteins)DNAJournal of molecular evolution
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Interspecies comparison of neuroglobin, cytoglobin and myoglobin: Sequence evolution and candidate regulatory elements

2003

Neuroglobin and cytoglobin are two novel members of the vertebrate globin family. Their physiological role is poorly understood, although both proteins bind oxygen reversibly and may be involved in cellular oxygen homeostasis. Here we investigate the selective constraints on coding and non-coding sequences of the neuroglobin and cytoglobin genes in human, mouse, rat and fish. Neuroglobin and cytoglobin are highly conserved, displaying very low levels of non-synonymous nucleotide substitutions. An oxygen supply function predicts distinct modes of gene regulation, involving hypoxia-responsive transcription factors. To detect conserved candidate regulatory elements, we compared the neuroglobin…

Molecular Sequence DataNeuroglobinNerve Tissue ProteinsSequence alignmentRegulatory Sequences Nucleic AcidBiologyMiceSpecies SpecificityGeneticsAnimalsHumansGlobinMolecular BiologyGeneGenetics (clinical)MammalsGeneticsRegulation of gene expressionBinding SitesBase SequenceMyoglobinCytoglobinFishesDNAMRNA stabilizationBiological EvolutionGlobinsRatsOxygenGene Expression RegulationRegulatory sequenceNeuroglobinSequence AlignmentTranscription FactorsCytogenetic and Genome Research
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Putative evolutionary origin of plasmids carrying the genes involved in leucine biosynthesis in Buchnera aphidicola (endosymbiont of aphids)

1997

An 8.5-kb plasmid encoding genes (leuABCD) involved in leucine biosynthesis and a small plasmid of 1.74 kb of yet unknown function were found in the intracellular symbiont, Buchnera aphidicola, of two divergent aphid species, Thelaxes suberi and Tetraneura caerulescens, respectively. The leuABCD-carrying plasmid (pBTs1) was amplified from total aphid DNA by inverse long PCR, using outwardly oriented oligonucleotide primers specific to leuA. The resulting 8.2-kb PCR fragment as well as the 1.74-kb plasmid (pBTc1) were cloned and sequenced. pBTs1 differed from a previously described B. aphidicola plasmid (pRPE) of the aphid Rhopalosiphum padi by the presence of a small heat shock gene (ibp) a…

Molecular Sequence DataReplication OriginRegulatory Sequences Nucleic AcidMicrobiologyDNA RibosomalEvolution MolecularOpen Reading FramesPlasmidPhylogeneticsLeucineGram-Negative BacteriaAnimalsRepliconAmino Acid SequenceMolecular BiologyGenePhylogenyGeneticsbiologyBase SequenceSequence Homology Amino AcidNucleic acid sequenceRibosomal RNAbiology.organism_classificationOpen reading frameGenes BacterialAphidsBuchneraPlasmidsResearch Article
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Conserved Structure and Promoter Sequence Similarity in the Mouse and Human Genes Encoding the Zinc Finger Factor BERF-1/BFCOL1/ZBP-89

2001

Abstract We have characterized the genomic structure of the mouse Zfp148 gene encoding Beta-Enolase Repressor Factor-1 (BERF-1), a Kruppel-like zinc finger protein involved in the transcriptional regulation of several genes, which is also termed ZBP-89, BFCOL1. The cloned Zfp148 gene spans 110 kb of genomic DNA encompassing the 5′-end region, 9 exons, 8 introns, and the 3′-untranslated region. The promoter region displays the typical features of a housekeeping gene: a high G+C content and the absence of canonical TATA and CAAT boxes consistent with the multiple transcription initiation sites determined by primary extension analysis. Computer-assisted search in the human genome database allo…

Molecular Sequence DataResponse elementBiophysicsCodon InitiatorRegulatory Sequences Nucleic AcidBiologyBiochemistryConserved non-coding sequenceMiceExonAnimalsHumansPromoter Regions GeneticMolecular BiologyGeneConserved SequenceGeneticsZinc fingerBase SequenceAlternative splicingIntronZinc FingersPromoterExonsCell BiologyIntronsDNA-Binding ProteinsAlternative Splicing5' Untranslated RegionsTranscription FactorsBiochemical and Biophysical Research Communications
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Isolation of the DNA minisatellite probe MZ 1.3 and its application to DNA ‘fingerprinting’ analysis

1990

Abstract A minisatellite probe, MZ 1.3, detecting hypervariable fragment patterns was isolated from a human genomic library. A repetitive sequence of 27 bp length was identified which is contained in the probe approx. 40 times. The MZ 1.3 repeat shows variable homology of 53–73% to the repetitive sequence of the protein III gene of the bacteriophage M13 genome. Polymorphic restriction fragment patterns were found with MZ 1.3 using the enzymes Hinf I, BstN I, Hae III, Mbo I, PstI PvuII , and Rsa I. An average of 18 polymorphic fragments was observed using Hinf I as enzyme. The band sharing frequency after Hinf I digestion among unrelated individuals was determined to be 23.8 ± 7.2%. An examp…

Molecular Sequence DataRestriction MappingDNA SatelliteHomology (biology)Pathology and Forensic MedicineRestriction fragmentchemistry.chemical_compoundHumansGenomic libraryGeneRepetitive Sequences Nucleic AcidGeneticsGenomic LibraryBase SequencebiologyNucleotide MappingDNAMolecular biologyBlotting SouthernVariable number tandem repeatMinisatelliteDNA profilingchemistrybiology.proteinDNA ProbesLawPolymorphism Restriction Fragment LengthDNAForensic Science International
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Comparative genomic sequencing reveals a strikingly similar architecture of a conserved syntenic region on human chromosome 11p15.3 (including gene S…

2001

Comparative genomics is a superior way to identify phylogenetically conserved features like genes or regions involved in gene regulation. The comparison of extended orthologous chromosomal regions should also reveal other characteristic traits essential for chromosome or gene function. In the present study we have sequenced and compared a region of conserved synteny from human chromosome 11p15.3 and mouse chromosome 7. In human, this region is known to contain several genes involved in the development of various disorders like Beckwith-Wiedemann overgrowth syndrome and other tumor diseases. Furthermore, in the neighboring chromosome region 11p15.5 extensive imprinting of genes has been repo…

Molecular Sequence DataeducationGenomicsBiologyChromosomesContig MappingMiceGene OrderGeneticsAnimalsHumansCloning MolecularMolecular BiologyGeneConserved SequenceGenetics (clinical)Repetitive Sequences Nucleic AcidSyntenyRegulation of gene expressionChromosome 7 (human)Comparative genomicsGeneticsChromosomes Human Pair 11Tumor Suppressor ProteinsGenomic sequencingChromosomeSequence Analysis DNAGC Rich SequenceDNA-Binding ProteinsCytogenetic and Genome Research
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Differential impact of allelic ratio and insertion site in FLT3-ITD-positive AML with respect to allogeneic transplantation.

2014

The objective was to evaluate the prognostic and predictive impact of allelic ratio and insertion site (IS) of internal tandem duplications (ITDs), as well as concurrent gene mutations, with regard to postremission therapy in 323 patients with FLT3-ITD-positive acute myeloid leukemia (AML). Increasing FLT3-ITD allelic ratio (P = .004) and IS in the tyrosine kinase domain 1 (TKD1, P = .06) were associated with low complete remission (CR) rates. After postremission therapy including intensive chemotherapy (n = 121) or autologous hematopoietic stem cell transplantation (HSCT, n = 17), an allelic ratio ≥ 0.51 was associated with an unfavorable relapse-free (RFS, P = .0008) and overall survival …

OncologyAdultmedicine.medical_specialtyAllogeneic transplantationMyeloidAdolescentmedicine.medical_treatmentImmunologyDNA Mutational AnalysisHematopoietic stem cell transplantationBiologyGene mutationBiochemistryYoung AdultGene FrequencyInternal medicineGene DuplicationGene duplicationmedicineHumansTransplantation HomologousAllelesHematopoietic Stem Cell TransplantationMyeloid leukemiaCell BiologyHematologyMiddle Agedmedicine.diseaseProtein Structure TertiaryTransplantationLeukemiaLeukemia Myeloid AcuteMutagenesis Insertionalmedicine.anatomical_structureTreatment Outcomefms-Like Tyrosine Kinase 3Tandem Repeat SequencesImmunologyBlood
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