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PMID: 3517633 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

The relative cytotoxicity and mutagenicity of cyclobutane pyrimidine dimers and (6-4) photoproducts in Escherichia coli cells.

Mutation research ·Vol. 161 ·No. 1 ·1986-06-00 ·Pages 9-17

Tang MS, Hrncir J, Mitchell D, Ross J, Clarkson J

Abstract

In order to calculate the relative cytotoxicity and mutagenicity of (5-6) cyclobutane pyrimidine dimers and (6-4) photoproducts, we have measured survival and mutation induction in UV-irradiated excision-deficient E. coli uvrA cells, with or without complete photoreactivation of the (5-6) dimers. Radioimmunoassays with specificity for (5-6) dimers or (6-4) photoproducts have shown that maximum photoreactivation eliminates all of the (5-6) dimers produced up to 10 Jm-2 254-nm light, while it has no effect on (6-4) photoproducts. These results were confirmed by measuring the frequency of T4 endonuclease V-sensitive sites. Based on the best fit equations for survival and mutation induction, we have found that the calculated cytotoxicity of (6-4) photoproducts is similar to that of (5-6) dimers; however, the former is much more mutagenic than the latter.

MeSH Terms
Dose-Response Relationship, Radiation Escherichia coli/cytology,drug effects,radiation effects Kinetics Mutagenicity Tests/methods Mutagens/pharmacology Mutation Pyrimidine Dimers/pharmacology Ultraviolet Rays
Chemicals
Mutagens Pyrimidine Dimers
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Tang M S
Hrncir J
Mitchell D
Ross J
Clarkson J
Article Info
Journal
Mutation research
Abbr.
Mutat Res
ISSN
0027-5107
Published
1986-06-00
Pages
9-17
Language
English
Region
Netherlands
NLM ID
0400763
Subset
IM
Grants
NCI NIH HHS · CA-24540 · United States
NIEHS NIH HHS · ES-03124 · United States
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