Host cell RecA activates a mobile element-encoded mutagenic DNA polymerase. Issue 12 (23rd June 2022)

• Record Type: Journal Article
• Authors: Ojha, Debika; Jaszczur, Malgorzata M; Sikand, Adhirath; McDonald, John P; Robinson, Andrew; van Oijen, Antoine M; Mak, Chi H; Pinaud, Fabien; Cox, Michael M; Woodgate, Roger; Goodman, Myron F
• Is Part Of: Nucleic acids research. Volume 50:Issue 12(2022)
• Page Start: 6854
• Page End: 6869
• Publication Date: 2022-06-23
• Subjects: Nucleic acids -- Periodicals; Molecular biology -- Periodicals; 572.805
• DOI: 10.1093/nar/gkac515
• Languages: English
• ISSNs: 0305-1048

Abstract

Abstract: Homologs of the mutagenic Escherichia coli DNA polymerase V (pol V) are encoded by numerous pathogens and mobile elements. We have used Rum pol (RumA′2 B), from the integrative conjugative element (ICE), R391, as a model mobile element-encoded polymerase (MEPol). The highly mutagenic Rum pol is transferred horizontally into a variety of recipient cells, including many pathogens. Moving between species, it is unclear if Rum pol can function on its own or requires activation by host factors. Here, we show that Rum pol biochemical activity requires the formation of a physical mutasomal complex, Rum Mut, containing RumA′2 B-RecA-ATP, with RecA being donated by each recipient bacteria. For R391, Rum Mut specific activities in vitro and mutagenesis rates in vivo depend on the phylogenetic distance of host-cell RecA from E. coli RecA. Rum pol is a highly conserved and effective mobile catalyst of rapid evolution, with the potential to generate a broad mutational landscape that could serve to ensure bacterial adaptation in antibiotic-rich environments leading to the establishment of antibiotic resistance.