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PMID: 1944363 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Mechanisms of spontaneous mutation in DNA repair-proficient Escherichia coli.

Mutation research ·Vol. 250 ·No. 1-2 ·1991-00-00 ·Pages 55-71

Halliday JA, Glickman BW

Abstract

This paper describes the DNA sequence analysis of 729 independent spontaneous lacI- mutations. This total is comprised of 478 novel mutations and 251 previously described events, and therefore should allow a more comprehensive view of spontaneous mutation in Escherichia coli. The spectrum is dominated by a hotspot (71% of all events). Mutations at this site consist of related addition and deletion events involving a number of repetitive sequences. Here we discuss how the frequency and proportion of these events vary in different DNA repair-deficient genetic backgrounds. The distribution of non-hotspot events includes base substitutions (38%), deletions (35%), frameshifts (14%), duplications (4%) and insertion elements (4%). G:C----A:T events dominate among base substitutions, while G:C----C:G events are the least common; the remaining types of base substitution are equally represented. Among deletions, a significant number do not display repeated sequences at their endpoints (26/72). However, almost all multiply recovered events (15/17) possess repeated sequences capable of accounting for the deletion endpoints. Similarly, over half of all duplications recovered (5/7) display repeated endpoints. Single-base frameshifts are equally divided between A:T and G:C sites, in each case (-) 1 events occur 3-fold more frequently that (+) 1 events. A comparative analysis of each mutational class recovered to lacI- spectra available in a variety of DNA repair/metabolism-deficient strains is presented here in an attempt to assess possible contributions from chemical, physical and enzymic sources of damage.

MeSH Terms
Base Sequence DNA Repair DNA, Bacterial Escherichia coli/genetics Frameshift Mutation Molecular Sequence Data Mutation
Chemicals
DNA, Bacterial
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Halliday J A
Department of Biology, York University, Toronto, Ont., Canada.
Glickman B W
Article Info
Journal
Mutation research
Abbr.
Mutat Res
ISSN
0027-5107
Published
1991-00-00
Pages
55-71
Language
English
Region
Netherlands
NLM ID
0400763
Subset
IM
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