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RESEARCH PRODUCT
Chromatin structure of transposon Tn903 cloned into a yeast plasmid
Emilia MatallanaJosél. RodríguezLuis FrancoJ. E. Perez-ortinFrancisco Estruchsubject
Transposable elementGeneticsInverted repeatGenes FungalRestriction MappingSaccharomyces cerevisiaeSpheroplastsBiologyOrigin of replicationChromatinNucleosomesChromatinchemistry.chemical_compoundTransformation GeneticPlasmidchemistryDNA Transposable ElementsDeoxyribonuclease INucleosomeCloning MolecularDNA FungalDeoxyribonuclease IMolecular BiologyDNAPlasmidsdescription
Transposon Tn903 contains the APH gene for kanamycin resistance, which is active in yeast [A. Jiménez and J. Davies (1980) Nature (London) 287, 869-871] and is flanked by two inverted repeats (IR) 1057 bp long. When plasmid pAJ50, carrying Tn903 and the 2-microns circle origin of replication, is cloned into Saccharomyces cerevisiae, nucleosomes are assembled in vivo on the prokaryotic DNA of the transposon. Indirect end labeling revealed that three nucleosomes are preferentially positioned on symmetrical sequences from both IRs. DNase I digestion also confirmed that the chromatin structure is symmetrical in both IRs. This suggests that sequence determinants are decisive for chromatin structure in these regions. We have calculated the rotational and translational fits [H. R. Drew and C. R. Calladine (1987) J. Mol. Biol. 195, 143-173] for the Tn903 sequence and the results indicate that the nucleosome positioning on the IRs is sequence-directed. Nucleosome deposition on the APH gene also occurs, but no clear positioning exists. Some sequence preference for positioning nucleosomes on the promoter can be predicted, especially from the translational fit. Experimental data indicate, however, that nucleosomes are absent from the promoter. Therefore, chromatin can be organized on prokaryotic DNA in a manner that resembles the typical eukaryotic chromatin structure.
year | journal | country | edition | language |
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1989-09-01 | Plasmid |