PMID:14573598

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Citation

Shen, X, Woodgate, R and Goodman, MF (2003) Escherichia coli DNA polymerase V subunit exchange: a post-SOS mechanism to curtail error-prone DNA synthesis. J. Biol. Chem. 278:52546-50

Abstract

DNA polymerase V consisting of a heterotrimer composed of one molecule of UmuC and two molecules of UmuD' (UmuD'2C) is responsible for SOS damage-induced mutagenesis in Escherichia coli. Here we show that although the UmuD'2C complex remains intact through multiple chromatographic steps, excess UmuD, the precursor to UmuD', displaces UmuD' from UmuD'2C by forming a UmuDD' heterodimer, while UmuC concomitantly aggregates as an insoluble precipitate. Although soluble UmuD'2C is readily detected when the two genes are co-transcribed and translated in vitro, soluble UmuD2C or UmuDD'C are not detected. The subunit exchange between UmuD'2C and UmuD offers a biological means to inactivate error-prone polymerase V following translesion synthesis, thus preventing mutations from occurring on undamaged DNA.

Links

PubMed Online version:10.1074/jbc.M310127200

Keywords

Cross-Linking Reagents/pharmacology; DNA/biosynthesis; DNA Damage; DNA-Directed DNA Polymerase/chemistry; Dimerization; Dose-Response Relationship, Drug; Electrophoresis, Polyacrylamide Gel; Escherichia coli/enzymology; Escherichia coli Proteins/chemistry; Models, Biological; Mutagenesis; Plasmids/metabolism; Protein Binding; Protein Biosynthesis; Protein Structure, Tertiary; Serine Endopeptidases/chemistry; Transcription, Genetic

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