1. Academic Validation
  2. Transcriptional repression facilitates RNA:DNA hybrid accumulation at DNA double-strand breaks

Transcriptional repression facilitates RNA:DNA hybrid accumulation at DNA double-strand breaks

  • Nat Cell Biol. 2025 Jun;27(6):992-1005. doi: 10.1038/s41556-025-01669-y.
Florian Saur # 1 Emma Lesage # 1 Lea Pradel 1 Sarah Collins 1 Anne-Laure Finoux 1 Emile Alghoul 1 Benjamin Le Bozec 1 Vincent Rocher 1 Romane Carette 1 Nadine Puget 1 Marie Couralet 1 Melanie Petiot 1 Thomas Clouaire 2 3 Aline Marnef 4 Gaëlle Legube 5
Affiliations

Affiliations

  • 1 MCD, Centre de Biologie Intégrative (CBI), CNRS, Université de Toulouse UT, Toulouse, France.
  • 2 MCD, Centre de Biologie Intégrative (CBI), CNRS, Université de Toulouse UT, Toulouse, France. [email protected].
  • 3 Institut National de la Santé et de la Recherche Médicale (INSERM), Paris, France. [email protected].
  • 4 MCD, Centre de Biologie Intégrative (CBI), CNRS, Université de Toulouse UT, Toulouse, France. [email protected].
  • 5 MCD, Centre de Biologie Intégrative (CBI), CNRS, Université de Toulouse UT, Toulouse, France. [email protected].
  • # Contributed equally.
Abstract

RNA:DNA hybrids accumulate at DNA double-strand breaks (DSBs) and were shown to regulate homologous recombination repair. The mechanism responsible for the formation of these non-canonical RNA:DNA structures remains unclear although they were proposed to arise consequently to RNA polymerase II or III loading followed by DSB-induced de novo transcription at the break site. Here, we found no evidence of RNA polymerase recruitment at DSBs. Rather, strand-specific R-loop mapping revealed that RNA:DNA hybrids are mainly generated at DSBs occurring in transcribing loci, from the hybridization of pre-existing RNA to the 3' overhang left by DNA end resection. We further identified the H3K4me3 reader spindlin 1 and the transcriptional regulator PAF1 as factors promoting RNA:DNA hybrid accumulation at DSBs, through their role in mediating transcriptional repression in cis to DSBs. Altogether, we provide evidence that RNA:DNA hybrids accumulate at DSBs occurring in transcribing loci as a result of DSB-induced transcriptional shut down.

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