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Chromatin bodies: isolation, subfractionation and physical characterization
Author(s) -
Ada L. Olins,
Robert D. Carlson,
E.B. Wright,
Donald E. Olins
Publication year - 1976
Publication title -
nucleic acids research
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/3.12.3271
Subject(s) - ultracentrifuge , micrococcal nuclease , biology , chromatin , monomer , dna , analytical ultracentrifugation , histone , sedimentation equilibrium , electron microscope , biochemistry , microbiology and biotechnology , centrifugation , chromatography , nucleosome , chemistry , polymer , physics , organic chemistry , optics
Monomer chromatin subunit particles (nu1) have been isolated in gram quantities by large-scale zonal centrifugation of micrococcal nuclease digests of chicken erythrocyte nuclei. nu1 can be stored, apparently indefinitely, frozen in 0.2 mM EDTA (pH 7.0) at less than or equal to 25 degrees C. Aliquots of the stored monomers have been subfractionated by dialysis against 0.1 M KCl buffers into a soluble fraction containing equimolar amounts of H4, H3, H2A, H2B associated with a DNA fragment of approximately 130-140 nucleotide pairs, and a precipitated fraction containing all of the histones including H5 and H1 associated with DNA fragments. The total nu1 and the KCl-soluble fraction of nu1 have been examined by sedimentation, diffusion, sedimentation equilibrium ultracentrifugation, low-angle X-ray diffraction, and electron microscopy. Physical parameters from all of these techniques are presented and correlated in this study.

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