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RNA:DNA hybrids from Okazaki fragments contribute to establish the Ku-mediated barrier to replication-fork degradation.
Audoynaud, Charlotte; Schirmeisen, Kamila; Ait Saada, Anissia; Gesnik, Armelle; Fernández-Varela, Paloma; Boucherit, Virginie; Ropars, Virginie; Chaudhuri, Anusha; Fréon, Karine; Charbonnier, Jean-Baptiste; Lambert, Sarah A E.
Affiliation
  • Audoynaud C; Institut Curie, Université PSL, CNRS UMR3348, 91400 Orsay, France; Université Paris-Saclay, CNRS UMR3348, 91400 Orsay, France; Ligue Nationale Contre le cancer (équipe labélisée), Orsay, France.
  • Schirmeisen K; Institut Curie, Université PSL, CNRS UMR3348, 91400 Orsay, France; Université Paris-Saclay, CNRS UMR3348, 91400 Orsay, France; Ligue Nationale Contre le cancer (équipe labélisée), Orsay, France.
  • Ait Saada A; Institut Curie, Université PSL, CNRS UMR3348, 91400 Orsay, France; Université Paris-Saclay, CNRS UMR3348, 91400 Orsay, France; Ligue Nationale Contre le cancer (équipe labélisée), Orsay, France.
  • Gesnik A; Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), 91198 Gif-sur-Yvette, France.
  • Fernández-Varela P; Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), 91198 Gif-sur-Yvette, France.
  • Boucherit V; Institut Curie, Université PSL, CNRS UMR3348, 91400 Orsay, France; Université Paris-Saclay, CNRS UMR3348, 91400 Orsay, France; Ligue Nationale Contre le cancer (équipe labélisée), Orsay, France.
  • Ropars V; Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), 91198 Gif-sur-Yvette, France.
  • Chaudhuri A; Institut Curie, Université PSL, CNRS UMR3348, 91400 Orsay, France; Université Paris-Saclay, CNRS UMR3348, 91400 Orsay, France; Ligue Nationale Contre le cancer (équipe labélisée), Orsay, France.
  • Fréon K; Institut Curie, Université PSL, CNRS UMR3348, 91400 Orsay, France; Université Paris-Saclay, CNRS UMR3348, 91400 Orsay, France; Ligue Nationale Contre le cancer (équipe labélisée), Orsay, France.
  • Charbonnier JB; Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), 91198 Gif-sur-Yvette, France.
  • Lambert SAE; Institut Curie, Université PSL, CNRS UMR3348, 91400 Orsay, France; Université Paris-Saclay, CNRS UMR3348, 91400 Orsay, France; Ligue Nationale Contre le cancer (équipe labélisée), Orsay, France. Electronic address: sarah.lambert@curie.fr.
Mol Cell ; 83(7): 1061-1074.e6, 2023 04 06.
Article in En | MEDLINE | ID: mdl-36868227
ABSTRACT
Nonhomologous end-joining (NHEJ) factors act in replication-fork protection, restart, and repair. Here, we identified a mechanism related to RNADNA hybrids to establish the NHEJ factor Ku-mediated barrier to nascent strand degradation in fission yeast. RNase H activities promote nascent strand degradation and replication restart, with a prominent role of RNase H2 in processing RNADNA hybrids to overcome the Ku barrier to nascent strand degradation. RNase H2 cooperates with the MRN-Ctp1 axis to sustain cell resistance to replication stress in a Ku-dependent manner. Mechanistically, the need of RNaseH2 in nascent strand degradation requires the primase activity that allows establishing the Ku barrier to Exo1, whereas impairing Okazaki fragment maturation reinforces the Ku barrier. Finally, replication stress induces Ku foci in a primase-dependent manner and favors Ku binding to RNADNA hybrids. We propose a function for the RNADNA hybrid originating from Okazaki fragments in controlling the Ku barrier specifying nuclease requirement to engage fork resection.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Schizosaccharomyces / RNA Type of study: Prognostic_studies Language: En Journal: Mol Cell Journal subject: BIOLOGIA MOLECULAR Year: 2023 Document type: Article Affiliation country: France

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Schizosaccharomyces / RNA Type of study: Prognostic_studies Language: En Journal: Mol Cell Journal subject: BIOLOGIA MOLECULAR Year: 2023 Document type: Article Affiliation country: France