Search results for "genetics [Neuropeptide Y]"

showing 3 items of 53 documents

Epigenetic Status of an Adenovirus Type 12 Transgenome upon Long-Term Cultivation in Hamster Cells

2007

ABSTRACT The epigenetic status of integrated adenovirus type 12 (Ad12) DNA in hamster cells cultivated for about 4 decades has been investigated. Cell line TR12, a fibroblastic revertant of the Ad12-transformed epitheloid hamster cell line T637 with 15 copies of integrated Ad12 DNA, carries one Ad12 DNA copy plus a 3.9-kbp fragment from a second copy. The cellular insertion site for the Ad12 integrate, identical in both cell lines, is a >5.2-kbp inverted DNA repeat. The Ad12 transgenome is packaged around nucleosomes. The cellular junction is more sensitive to micrococcal nuclease at Ad12-occupied sites than at unoccupied sites. Bisulfite sequencing reveals complete de novo methylation i…

Virus CultivationTranscription GeneticVirus IntegrationvirusesImmunologyBisulfite sequencingHamsterMicrobiologyAdenoviridaeCell LineEpigenesis GeneticHistoneschemistry.chemical_compoundEpigenetics of physical exerciseProvirusesCricetinaeVirologyAnimalsMicrococcal NucleaseNucleosomeMethylated DNA immunoprecipitationEpigeneticsCell Line TransformedbiologyAcetylationDNADNA Methylationbiochemical phenomena metabolism and nutritionMolecular biologyVirus-Cell InteractionsNucleosomesstomatognathic diseaseschemistryInsect ScienceDNA Viralbiology.proteinDNAMicrococcal nucleaseJournal of Virology
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Genetic and Chemical Modifiers Of A CUG Toxicity Model in Drosophila

2007

Non-coding CUG repeat expansions interfere with the activity of human Muscleblind-like (MBNL) proteins contributing to myotonic dystrophy 1 (DM1). To understand this toxic RNA gain-of-function mechanism we developed a Drosophila model expressing 60 pure and 480 interrupted CUG repeats in the context of a non-translatable RNA. These flies reproduced aspects of the DM1 pathology, most notably nuclear accumulation of CUG transcripts, muscle degeneration, splicing misregulation, and diminished Muscleblind function in vivo. Reduced Muscleblind activity was evident from the sensitivity of CUG-induced phenotypes to a decrease in muscleblind genetic dosage and rescue by MBNL1 expression, and furthe…

congenital hereditary and neonatal diseases and abnormalitiesGene Dosagelcsh:MedicineRNA-binding proteinBiologyEyechemistry.chemical_compoundTrinucleotide RepeatsAnimalsDrosophila ProteinsMyotonic DystrophyMBNL1lcsh:ScienceGeneGenetics and Genomics/Genetics of DiseaseGeneticsMessenger RNADNA Repeat ExpansionMultidisciplinaryAlternative splicinglcsh:RBrainNuclear ProteinsRNA-Binding ProteinsRNAPhenotypeCell biologyDisease Models AnimalGenetics and Genomics/Disease ModelschemistryRNA splicingDrosophilalcsh:QGenèticaResearch Article
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A leptin missense mutation associated with hypogonadism and morbid obesity

1998

medicine.medical_specialtyLeptin DeficiencyInsulin bloodGenetics of obesityLeptinBiologymedicine.diseaseObesityMorbid obesityEndocrinologyInternal medicineMutation (genetic algorithm)GeneticsmedicineMissense mutationNature Genetics
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