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PMID: 2160660 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

UV induced (6-4) photoproducts are distributed differently than cyclobutane dimers in nucleosomes.

Photochemistry and photobiology ·Vol. 51 ·No. 4 ·1990-04-00 ·Pages 411-7

Gale JM, Smerdon MJ

Abstract

We have compared the distributions of two stable UV photoproducts in nucleosome core DNA at the single-nucleotide level using a T4 polymerase-exonuclease mapping procedure. The distribution of pyrimidine-pyrimidone (6-4) dimers was uncovered by reversing the major UV photo-product, cis-syn cyclobutane pyrimidine dimer, with E. coli DNA photolyase and photoreactivating light. Whereas the distribution of total UV photoproducts in nucleosome core DNA forms a striking 10.3 base periodic pattern, the distribution of (6-4) dimers is much more random throughout the nucleosome core domain. Therefore, histone-DNA interactions in nucleosomes strongly modulate formation of the major class of UV-induced photoproducts, while having either a constant effect or no effect on (6-4) dimer formation.

MeSH Terms
Animals Cattle Chromatin/radiation effects DNA/radiation effects DNA-Directed DNA Polymerase/metabolism Exonucleases/metabolism Nucleosomes/radiation effects Nucleotide Mapping T-Phages/enzymology Thymus Gland/radiation effects Ultraviolet Rays
Chemicals
Chromatin Nucleosomes DNA DNA-Directed DNA Polymerase Exonucleases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Gale J M
Biochemistry/Biophysics Program, Washington State University, Pullman 99164-4660.
Smerdon M J
Article Info
Journal
Photochemistry and photobiology
Abbr.
Photochem Photobiol
ISSN
0031-8655
Published
1990-04-00
Pages
411-7
Language
English
Region
United States
NLM ID
0376425
Subset
IM
Grants
NIEHS NIH HHS · ES02614 · United States
NIEHS NIH HHS · ES03720 · United States
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