Protein-templated synthesis of dinucleotide repeat DNA by an antiphage reverse transcriptase

Abstract

Defense-associated reverse transcriptases (DRTs) are widespread bacterial antiphage systems that use unconventional mechanisms of polynucleotide synthesis. We show that DRT3, which comprises two distinct RTs (Drt3a and Drt3b) and a noncoding RnA (ncRnA), synthesizes alternating poly(GT/AC) double-stranded DnA. Cryo–electron microscopy structures at 2.6-angstrom resolution reveal a D3-symmetric 6:6:6 complex of Drt3a, Drt3b, and ncRnA. Drt3a produces the poly(GT) strand using a conserved ACACAC template within the ncRnA. notably, Drt3b synthesizes a complementary, protein-primed poly(AC) strand in the complete absence of a nucleic acid template, using conserved active site residues specific to Drt3b to enforce precise base alternation. These findings expand the functional landscape of nucleic acid polymerases, revealing a protein-templated mechanism for sequence-specific DnA synthesis.