Host cell RecA activates a mobile element-encoded mutagenic DNA polymerase.
Debika OjhaMalgorzata M JaszczurAdhirath SikandJohn P McDonaldAndrew RobinsonAntoine M van OijenChi H MakFabien PinaudMichael M CoxRoger WoodgateMyron F GoodmanPublished in: Nucleic acids research (2022)
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'2B), 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'2B-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.
Keyphrases
- escherichia coli
- single cell
- circulating tumor
- cell therapy
- single molecule
- induced apoptosis
- cell free
- mental health
- physical activity
- gram negative
- transcription factor
- structural basis
- stem cells
- antimicrobial resistance
- highly efficient
- microbial community
- bone marrow
- signaling pathway
- pseudomonas aeruginosa
- mesenchymal stem cells
- pi k akt
- human health
- anaerobic digestion
- sensitive detection
- antibiotic resistance genes