RecA-dependent or independent recombination of plasmid DNA generates a conflict with the host EcoKI immunity by launching restriction alleviation.
Mikhail SkutelDaria YanovskayaAlina DemkinaAleksandr ShenfeldOlga MusharovaKonstantin V SeverinovArtem IsaevPublished in: Nucleic acids research (2024)
Bacterial defence systems are tightly regulated to avoid autoimmunity. In Type I restriction-modification (R-M) systems, a specific mechanism called restriction alleviation (RA) controls the activity of the restriction module. In the case of the Escherichia coli Type I R-M system EcoKI, RA proceeds through ClpXP-mediated proteolysis of restriction complexes bound to non-methylated sites that appear after replication or reparation of host DNA. Here, we show that RA is also induced in the presence of plasmids carrying EcoKI recognition sites, a phenomenon we refer to as plasmid-induced RA. Further, we show that the anti-restriction behavior of plasmid-borne non-conjugative transposons such as Tn5053, previously attributed to their ardD loci, is due to plasmid-induced RA. Plasmids carrying both EcoKI and Chi sites induce RA in RecA- and RecBCD-dependent manner. However, inactivation of both RecA and RecBCD restores RA, indicating that there exists an alternative, RecA-independent, homologous recombination pathway that is blocked in the presence of RecBCD. Indeed, plasmid-induced RA in a RecBCD-deficient background does not depend on the presence of Chi sites. We propose that processing of random dsDNA breaks in plasmid DNA via homologous recombination generates non-methylated EcoKI sites, which attract EcoKI restriction complexes channeling them for ClpXP-mediated proteolysis.
Keyphrases
- escherichia coli
- rheumatoid arthritis
- disease activity
- high glucose
- dna repair
- dna damage
- crispr cas
- diabetic rats
- ankylosing spondylitis
- drug induced
- systemic lupus erythematosus
- circulating tumor
- klebsiella pneumoniae
- biofilm formation
- interstitial lung disease
- cell free
- single molecule
- oxidative stress
- transcription factor
- genome wide
- endothelial cells
- microbial community