Toxic antiphage defense proteins inhibited by intragenic antitoxin proteins.

Abstract

Recombination-promoting nuclease (Rpn) proteins are broadly distributed across bacterial phyla, yet their functions remain unclear. Here, we report that these proteins are toxin-antitoxin systems, comprised of genes-within-genes, that combat phage infection. We show the small, highly variable Rpn <i>C</i>-terminal domains (Rpn_S), which are translated separately from the full-length proteins (Rpn_L), directly block the activities of the toxic Rpn_L. The crystal structure of RpnA_S revealed a dimerization interface encompassing α helix that can have four amino acid repeats whose number varies widely among strains of the same species. Consistent with strong selection for the variation, we document that plasmid-encoded RpnP2_L protects <i>Escherichia coli</i> against certain phages. We propose that many more intragenic-encoded proteins that serve regulatory roles remain to be discovered in all organisms.