Abstract
Previously, we have shown that DNA in a small fraction (2-5%) of SV40 minichromosomes was torsionally strained and could be relaxed by treating minichromosomes with topoisomerase I. This fraction was enriched with endogeneous RNA polymerase II (Luchnik et al., 1982, EMBO J., 1, 1353). Here we show that one and the same fraction of SV40 minichromosomes is hypersensitive to DNAase I and is relaxable by topoisomerase I. Moreover, this fraction completely loses its hypersensitivity to DNAase I upon relaxation. The possibility that this fraction of minichromosomes can be represented by naked DNA is ruled out by the results of studying the kinetics of minichromosome digestion by DNAase I in comparison to digestion of pure SV40 DNA and by measuring the buoyant density of SV40 chromatin in equilibrium CsCl gradient. Our data obtained with SV40 minichromosomes may be relevant to the mechanism responsible for DNAase I hypersensitivity in the loops or domains of cellular chromatin.
MeSH Terms
Animals
Cells, Cultured
Chlorocebus aethiops
Chromatin/physiology,ultrastructure
DNA, Superhelical/genetics
DNA, Viral/genetics
Deoxyribonuclease I
Gene Expression Regulation
Nucleic Acid Conformation
Simian virus 40/genetics
Chemicals
Chromatin
DNA, Superhelical
DNA, Viral
Deoxyribonuclease I
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Luchnik A N
Bakayev V V
Yugai A A
Zbarsky I B
Georgiev G P
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