0000000000787904

AUTHOR

P. Cavolina

showing 4 related works from this author

Nalidixic acid-resistant V79 cells with reduced DNA topoisomerase II activity and amplification prone phenotype

1992

Spontaneously nalidixic acid-resistant lines (NAr lines) were selected from a V79 Chinese hamster cell line and phenotypically characterized. NAr lines showed an increased doubling time, a higher number of spontaneous SCE, and more interestingly, decreased DNA topoisomerase II activity. These lines were also cross-resistant to the eukaryotic topoisomerase II inhibitors etoposide and adriamycin, but showed the same level of sensitivity as the parental line to the DNA topoisomerase I inhibitor camptothecin. NAr lines were cross-resistant to other drugs, such as PALA, MTX and MPA, resistance to which has been shown to arise by amplification of the target genes. This last feature, together with…

Nalidixic acidCell SurvivalHealth Toxicology and MutagenesisDrug ResistanceAntineoplastic AgentsBiologyCell LineNalidixic Acidchemistry.chemical_compoundCricetulusCricetinaeGeneticsmedicineAnimalsTopoisomerase II InhibitorsMolecular BiologyGeneEtoposideEtoposideCell NucleusMesocricetusTopoisomeraseGene AmplificationNucleic Acid HybridizationDNADNA topoisomerase II activityMolecular biologyDNA Topoisomerases Type IIPhenotypeDNA Topoisomerases Type IchemistryDoxorubicinbiology.proteinTopoisomerase-II InhibitorSister Chromatid ExchangeDNACamptothecinmedicine.drugMutation Research/Fundamental and Molecular Mechanisms of Mutagenesis
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Localization of amplified CAD genes on rearranged chromosomes of Chinese hamster cells

2012

Chinese hamster cell lines carrying an amplified CAD region were selected from V79,B7 cells by their resistance to N-phosphonacetyl-L-aspartate (PALA). In one of the selected cell lines, SP PALA (inf1) (supR) L, an acrocentric chromosome with abnormally elongated q arms was identified as a marker for the PALA-resistant phenotype. The marker chromosome carried a homogeneously staining region close to a telomeric nucleolar organizer region. In the same region, localization of amplified CAD sequences was demonstrated by in situ hybridization. The marker chromosome was found to undergo extensive rearrangements. In particular, dicentric chromosomes, occurring with an unusually high incidence, we…

Geneticseducation.field_of_studybiologyMarker chromosomeClinical BiochemistryBiomedical EngineeringBioengineeringCell Biologybiology.organism_classificationMolecular biologyNucleolar Organizer RegionChinese hamsterDicentric chromosomeHomologous chromosomeeducationSmall supernumerary marker chromosomeChromosome 22Homogeneously Staining RegionBiotechnologyCytotechnology
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Crystal cell pattern modification in a melanotic tumor strain of Drosophila melanogaster.

1988

3rd instar larvae of the melanotic tumor tu-pb strain of Drosophila melanogaster hold a lower number of free-circulating crystal cells in their hemolymph than the wild type ones. This pattern could result from an abnormal retention of mature crystal cells in the hematopoietic organs, as the strong hemocyte melanization inside the lymph glands of heat-treated tu-pb larvae seems to demonstrate. Melanotic tumor formation and modification of the crystal cell pattern may be related.

Pharmacologyanimal structuresStrain (chemistry)biologyfungiWild typeTemperatureCell Biologybiology.organism_classificationCell biologyCellular and Molecular NeuroscienceHaematopoiesisDrosophila melanogasterGenesHemolymphImmunologyHemolymphMelanogasterMolecular MedicineInstarAnimalsLymphDrosophila melanogasterMolecular BiologyMelanomaExperientia
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Cytogenetic manifestations associated with the reversion, by gene amplification, at the HGPRT locus in V79 Chinese hamster cells.

1989

SummarySome HGPRT spontaneous revertants were isolated from a mutant line (E2) of V79 Chinese hamster cells and phenotypically characterized. Dot–Blot hybridization with a32P-Iabelled HGPRT probe revealed an increase in the number of HGPRT sequences in some of these revertants, suggesting the occurrence of gene amplification. Cytogenetic analysis performed in three of these revertants showed a characteristic abnormally banding region (ABR) on the elongated p arm of theXchromosome.In Situhybridization in one revertant (RHE2) showed that the amplified sequences reside on the p+arm of theXchromsome in two different localizations. Because of the very probable clonal origin of the revertant, the…

GeneticsGene Rearrangementmedicine.medical_specialtyHypoxanthine PhosphoribosyltransferaseCytogeneticsReversionGene AmplificationChromosomeHamsterKaryotypeGeneral MedicineGene rearrangementBiologybiology.organism_classificationMolecular biologyChinese hamsterCell LineCricetinaeMutationGeneticsmedicineAnimalsX chromosomeGenetical research
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