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Enhanced characterization of the thyA system for mutational analysis in Escherichia coli: Defining mutationally "hot" regions of the gene.
- Source :
-
Mutation research [Mutat Res] 2021 Jul-Dec; Vol. 823, pp. 111754. Date of Electronic Publication: 2021 May 25. - Publication Year :
- 2021
-
Abstract
- We have extensively characterized base substitution mutations in the 795 base pair (bp) long E. coli thyA gene to define as many of the base substitution mutational sites that inactivate the gene as possible. The resulting catalog of mutational sites constitutes a system with up to 5 times as many sites for monitoring each of the six base substitution mutations as the widely used rpoB/Rif <superscript>r</superscript> system. We have defined 75 sites for the G:C -> A:T transition, 68 sites for the G:C -> T:A transversion, 53 sites for the G:C -> C:G transversion, 49 sites for the A:T -> G:C transition, 39 sites for the A:T -> T:A transversion, and 59 sites for the A:T -> C:G transversion. The system is thus comprised of 343 base substitution mutations at 232 different base pairs, all of which can be sequenced with a single primer pair. This allows for the examination of mutational spectra using a more detailed probe of known mutations, while still allowing one to compare the number of repeated occurrences at specific sites. We have examined several mutagens and mutators with this system, and show its utility by looking at the spectrum of cisplatin, that has a single hotspot, underscoring the value of having as large an array of sites as possible at which one can monitor repeat occurrences. To test for regions of the gene that might be hotspots for a number of mutagens, or "hot" (mutaphilic) regions, we have looked at the ratio of mutations per set of an equal number of mutational sites throughout the gene. The resulting graphs suggest that there are "hot" regions at intervals, and this may reflect aspects of secondary structures, of the higher order structure of the chromosome, or perhaps the nucleoid structure of the chromosome plus histone-like protein complexes.<br /> (Copyright © 2021 The Authors. Published by Elsevier B.V. All rights reserved.)
- Subjects :
- 2-Aminopurine pharmacology
4-Nitroquinoline-1-oxide pharmacology
Azacitidine pharmacology
Base Sequence
Bromodeoxyuridine pharmacology
Cisplatin pharmacology
Codon
DNA Primers genetics
DNA Primers metabolism
Escherichia coli genetics
Escherichia coli metabolism
Ethyl Methanesulfonate pharmacology
Genetic Code
High-Throughput Nucleotide Sequencing
Mutagenesis
Chromosomes, Bacterial drug effects
Escherichia coli drug effects
Genes, Bacterial
Mutagens pharmacology
Mutation
Subjects
Details
- Language :
- English
- ISSN :
- 1873-135X
- Volume :
- 823
- Database :
- MEDLINE
- Journal :
- Mutation research
- Publication Type :
- Academic Journal
- Accession number :
- 34091127
- Full Text :
- https://doi.org/10.1016/j.mrfmmm.2021.111754