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PMID: 291002 Published · ppublish English Journal Article

In vitro core particle and nucleosome assembly at physiological ionic strength.

Ruiz-Carrillo A, Jorcano JL, Eder G, Lurz R

Abstract

Nucleosome core particles have been efficiently assembled in vitro by direct interaction of histones and DNA at physiological ionic strength, as assayed by digestion with DNases, supercoiling of relaxed circular DNA, and electron microscopy. Reconstitution was achieved either by the simultaneous addition of all core histones, or by the sequential binding of H3 . H4 tetramer and H2A . H2B dimer to DNA. Micrococcal nuclease digestion and electron microscopy studies indicated that there is heterogeneity in the spacings at which core particles are assembly on the DNA. Length measurements of oligomeric DNA produced during the course of the digestion suggest that the core histone octamer can organize 167 (+/- 4) rather than 145 base pairs of DNA, the extra 20 base pairs being quickly digested. Binding of histone H1 to core particles resulted in the protection of about 165 base pairs of DNA from nuclease attack. Because the core histone octamer is fully dissociated into H3 . H4 tetramer and H2A . H2B dimer at physiological ionic strength, our results would suggest that in vivo core particle assembly may also occur by interaction of these two complexes on the nascent DNA.

MeSH Terms
Animals Chickens Chromatin/metabolism DNA/metabolism Erythrocytes/metabolism Histones/metabolism In Vitro Techniques Nucleic Acid Conformation Nucleosomes/metabolism Osmolar Concentration Protein Conformation
Chemicals
Chromatin Histones Nucleosomes DNA
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Ruiz-Carrillo A
Jorcano J L
Eder G
Lurz R
References (35)
35 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1979-07-00
Pages
3284-8
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC383809
Subset
IM
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