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PMID: 6373019 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Specificity of mutagenesis resulting from the induction of the SOS system in the absence of mutagenic treatment.

Cell ·Vol. 37 ·No. 2 ·1984-06-00 ·Pages 675-82

Miller JH, Low KB

Abstract

Strains in which the E. coli SOS system is continuously induced, in the absence of mutagenic treatment, have been used to generate nonsense mutations in the lacl gene. The examination of over 600 independently occurring amber and ochre mutations reveals that inducing the SOS system stimulates specifically G:C----T:A and, to a lesser extent, A:T----T:A transversions. This specificity is similar to that seen for a number of carcinogens that form bulky adducts to DNA, such as benzo(a)pyrene diolepoxide (BPDE) and aflatoxin B1 (AFB1), and which are dependent on the SOS system to mutagenize bacteria. However, G:C----T:A transversions resulting from SOS induction alone display a unique site specificity. One possibility is that the SOS-induced mutations result from cryptic, spontaneous lesions, such as apurinic sites, which cannot induce the SOS system themselves but which can target mutations once the SOS system is induced.

MeSH Terms
Animals Carcinogens/toxicity DNA Repair Escherichia coli/genetics Genotype Mutagens Mutation Species Specificity
Chemicals
Carcinogens Mutagens
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Miller J H
Low K B
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1984-06-00
Pages
675-82
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NCI NIH HHS · CA06519 · United States
NIGMS NIH HHS · GM 32184 · United States
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