
doi: 10.1007/bf00319831
pmid: 1095320
It is reported that chromatin can be prepared from highly purified polytene nuclei from the salivary glands of third instar larvae of Drosophila hydei; such chromatin differs from that of diploid nuclei mainly by deficiencies in certain nonhistone chromosomal proteins. It is suggested that these proteins are important components of constitutive heterochromatin, which is severely underrepresented in polytene chromosomes. Chromosome morphology, including the pattern of induced puffs, is maintained throughout the mass isolation of glands and sucrose gradient purification of nuclei, as indicated by studies on temperature-shocked and control larvae. No significant alteration in the chromosomal proteins following puff induction by heat shock could be detected on analysis of the isolated protein fractions by disc gel electrophoresis. More sensitive techniques must be developed to study the apparent rearrangement or accumulation of protein at puff sites, and to elucidate the role of this protein in gene activation.
Cell Nucleus, Ecdysone, Embryo, Nonmammalian, Hot Temperature, Cells, Proteins, Centrifugation, Cell Fractionation, Electrophoresis, Disc, Diploidy, Chromatin, Chromosomes, Salivary Glands, Histones, Genes, Heterochromatin, Larva, Animals, Drosophila, Microscopy, Phase-Contrast
Cell Nucleus, Ecdysone, Embryo, Nonmammalian, Hot Temperature, Cells, Proteins, Centrifugation, Cell Fractionation, Electrophoresis, Disc, Diploidy, Chromatin, Chromosomes, Salivary Glands, Histones, Genes, Heterochromatin, Larva, Animals, Drosophila, Microscopy, Phase-Contrast
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