Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Deoxyribonucleic acid excision repair in chromatin after ultraviolet irradiation of human fibroblasts in culture

Journal Article · · Biochemistry; (United States)
DOI:https://doi.org/10.1021/bi00585a019· OSTI ID:5473877
We have exposed confluent normal human fibroblasts to ultraviolet (UV) fluences of 5, 14, or 40 J/m/sup 2/ and monitored the specific activity of post-uv repair synthesis in chromatin with (/sup 3/H)thymidine pulses. We have shown that under conditions where no semiconservative deoxyribonucleic acid (DNA) synthesis is detectable, the specific activity of repair label one-fifth that in bulk DNA at all three uv fluences. On the other hand, the distribution of thymine-containing pyrimidine dimers in bulk and nuclease-resistant regions measured either immediately after irradiation or at later times showed no significant differences; preferential labeling of linker (nuclease-sensitive) DNA during repair synthesis is thus apparently not due to a predominance of uv-induced photoproducts in linker relative to core particle DNA in the nucleosoome. Pulse and pulse-chase experiments at 14 or 40 J/m/sup 2/ with normal human or repair-deficient xeroderma pigmentosum (XP) cells showed that at most 30% of repair label in all these cells shifts from nuclease-sensitive (linker) DNA to nuclease-resistant (core particle) DNA.
Research Organization:
Stanford Univ. Medical Center, CA
OSTI ID:
5473877
Journal Information:
Biochemistry; (United States), Journal Name: Biochemistry; (United States) Vol. 18:18; ISSN BICHA
Country of Publication:
United States
Language:
English