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How RNA transcripts coordinate DNA recombination and repair.

Shane McDevittTimur RusanovTatiana KentGurushankar ChandramoulyRichard T Pomerantz
Published in: Nature communications (2018)
Genetic studies in yeast indicate that RNA transcripts facilitate homology-directed DNA repair in a manner that is dependent on RAD52. The molecular basis for so-called RNA-DNA repair, however, remains unknown. Using reconstitution assays, we demonstrate that RAD52 directly cooperates with RNA as a sequence-directed ribonucleoprotein complex to promote two related modes of RNA-DNA repair. In a RNA-bridging mechanism, RAD52 assembles recombinant RNA-DNA hybrids that coordinate synapsis and ligation of homologous DNA breaks. In an RNA-templated mechanism, RAD52-mediated RNA-DNA hybrids enable reverse transcription-dependent RNA-to-DNA sequence transfer at DNA breaks that licenses subsequent DNA recombination. Notably, we show that both mechanisms of RNA-DNA repair are promoted by transcription of a homologous DNA template in trans. In summary, these data elucidate how RNA transcripts cooperate with RAD52 to coordinate homology-directed DNA recombination and repair in the absence of a DNA donor, and demonstrate a direct role for transcription in RNA-DNA repair.
Keyphrases
  • dna repair
  • dna damage
  • nucleic acid
  • circulating tumor
  • dna damage response
  • cell free
  • single molecule
  • oxidative stress
  • transcription factor
  • high throughput
  • big data
  • circulating tumor cells
  • drug induced