Group II intron-like reverse transcriptases function in double-strand break repair

Cell. 2022 Sep 29;185(20):3671-3688.e23. doi: 10.1016/j.cell.2022.08.014. Epub 2022 Sep 15.

Abstract

Bacteria encode reverse transcriptases (RTs) of unknown function that are closely related to group II intron-encoded RTs. We found that a Pseudomonas aeruginosa group II intron-like RT (G2L4 RT) with YIDD instead of YADD at its active site functions in DNA repair in its native host and when expressed in Escherichia coli. G2L4 RT has biochemical activities strikingly similar to those of human DNA repair polymerase θ and uses them for translesion DNA synthesis and double-strand break repair (DSBR) via microhomology-mediated end-joining (MMEJ). We also found that a group II intron RT can function similarly in DNA repair, with reciprocal active-site substitutions showing isoleucine favors MMEJ and alanine favors primer extension in both enzymes. These DNA repair functions utilize conserved structural features of non-LTR-retroelement RTs, including human LINE-1 and other eukaryotic non-LTR-retrotransposon RTs, suggesting such enzymes may have inherent ability to function in DSBR in a wide range of organisms.

Keywords: Alt-EJ; DNA repair polymerase; alternative end joining; high-throughput sequencing; insect R2 element; non-retroviral reverse transcriptase; targetron; thermostable group II intron reverse transcriptase.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine / genetics
  • DNA End-Joining Repair
  • DNA Repair
  • DNA-Directed RNA Polymerases / genetics
  • Humans
  • Introns
  • Isoleucine / genetics
  • RNA-Directed DNA Polymerase* / chemistry
  • Retroelements*

Substances

  • Retroelements
  • Isoleucine
  • RNA-Directed DNA Polymerase
  • DNA-Directed RNA Polymerases
  • Alanine