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PMID: 4084488 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Cyclobutane pyrimidine dimers and (6-4) photoproducts block polymerization by DNA polymerase I.

Biochemistry ·Vol. 24 ·No. 21 ·1985-10-08 ·Pages 5723-8

Chan GL, Doetsch PW, Haseltine WA

Abstract

Bipyrimidine cyclobutane dimers and 6-4'-(pyrimidin-2'-one)-pyrimidine photoproducts are the major adducts formed in DNA following exposure to ultraviolet light. The relationship between the type and frequency of UV-induced DNA damage and the effects of such damage on DNA replication were investigated. UV-irradiated M13 phage DNA was employed in polymerization reactions with the Kenow fragment of Escherichia coli DNA polymerase I. The locations and frequencies of polymerase termination events occurring within a defined sequence of M13 DNA were compared with measurements of the locations and frequencies of UV-induced DNA damage of the same DNA sequence by using UV-specific enzymatic and chemical methods. The results indicate that both cyclobutane dimers and (6-4) photoproducts quantitatively block polymerization by DNA polymerase I.

MeSH Terms
Coliphages/genetics DNA Polymerase I/antagonists & inhibitors DNA Replication/radiation effects DNA, Viral/radiation effects Dose-Response Relationship, Radiation Genes, Viral Kinetics Pyrimidine Dimers Pyrimidinones T-Phages/enzymology Templates, Genetic Ultraviolet Rays
Chemicals
DNA, Viral Pyrimidine Dimers Pyrimidinones DNA Polymerase I
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Chan G L
Doetsch P W
Haseltine W A
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1985-10-08
Pages
5723-8
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Grants
NCI NIH HHS · CA06753 · United States
NCI NIH HHS · CA25118 · United States
NCI NIH HHS · CA26716 · United States
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