Summary
DNA was extracted from etiolated plantlets ofPhaseolus coccineus L. and studied by means of thermal denaturation and reassociation kinetics and CsCl analytical ultracentrifugation. A DNA fraction reassociating within an equivalent Cot of 1.15 × 10−1 (fast renaturing DNA sequences; FRS) was found to constitute 20.8% of the total DNA, 6.8% of which is composed of palindromic sequences. Analytical CsCl gradient ultracentrifugation showed a large heavier satellite banding at 1.702 g/ml (main peak 1.692g/ml); this DNA fraction was shown to consist of different components with buoyant densities of 1.696, 1.702, 1.706, and 1.714g/ml. FRS and the satellite fraction banding at 1.702 g/ml (SAT) were hybridizedin situ to the polytene chromosomes in the embryo suspensor cells after having been labeled by the nick translation method. FRS proved to be almost exclusively localized in the heterochromatic chromosome regions and several chromosome ends; SAT was found to be confined, as a rule, in the centromeric and pericentromeric heterochromatin. Different labeling patterns were detected over chromosome regions bearing 18S + 25S or 5 S ribosomal RNA cistrons and over corresponding regions of different chromosome pairs. These results are discussed for the light they may throw on certain aspects of the structure and organization at the chromosomal level of theP. coccineus genome.
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Durante, M., Cremonini, R., Tagliasacchi, A.M. et al. Characterization and chromosomal localization of fast renaturing and satellite DNA sequences inPhaseolus coccineus . Protoplasma 137, 100–108 (1987). https://doi.org/10.1007/BF01281145
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DOI: https://doi.org/10.1007/BF01281145