Mutations produced by DNA polymerase III holoenzyme of Escherichia coli after in vitro synthesis in the absence of single-strand binding protein
Carraway, Margaretha ; Rewinski, Caroline ; Marinus, Martin G.
Carraway, Margaretha
Rewinski, Caroline
Marinus, Martin G.
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UMass Chan Affiliations
Document Type
Journal Article
Publication Date
1990-10-01
Keywords
Base Sequence
Chromosome Deletion
DNA Polymerase III
*DNA Replication
DNA Transposable Elements
DNA, Bacterial
DNA, Single-Stranded
Escherichia coli
Genes, Bacterial
Molecular Sequence Data
Mutation
Plasmids
Templates, Genetic
Tetracycline Resistance
Biochemistry, Biophysics, and Structural Biology
Pharmacology, Toxicology and Environmental Health
Chromosome Deletion
DNA Polymerase III
*DNA Replication
DNA Transposable Elements
DNA, Bacterial
DNA, Single-Stranded
Escherichia coli
Genes, Bacterial
Molecular Sequence Data
Mutation
Plasmids
Templates, Genetic
Tetracycline Resistance
Biochemistry, Biophysics, and Structural Biology
Pharmacology, Toxicology and Environmental Health
Subject Area
Embargo Expiration Date
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Abstract
Single-stranded plasmid DNA, containing the mnt gene, was replicated in vitro with DNA polymerase III holoenzyme. Escherichia coli mutH bacteria, defective in mismatch repair, were transformed with the products of in vitro synthesis. Mutations in mnt were readily identified and 33 out of 65 isolates were single base changes including transition, transversion and frameshift mutations. The remaining 32 isolates were deletions of apparently random length and substitutions (deletion/insertions). The intergenic deletions as well as the transition and frameshift mutations were identical to those previously isolated from mismatch repair-defective cells in vivo.
Source
Mol Microbiol. 1990 Oct;4(10):1645-52.
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PubMed ID
1963919