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  2. The PARP1-EXD2 axis orchestrates R-loop resolution to safeguard genome stability

The PARP1-EXD2 axis orchestrates R-loop resolution to safeguard genome stability

  • Nat Chem Biol. 2025 Jun 27. doi: 10.1038/s41589-025-01952-x.
Zhaoshuang Li # 1 2 3 4 Yu Liu # 2 3 Yuanhui Liu # 5 Yiting Zhang 2 3 Michael Shing Yan Huen 6 Huasong Lu 2 Zhigang Zhang 1 Jianwei Zhou 7 Dong Fang 8 Ting Liu 9 10 Jun Huang 11 12 13 14
Affiliations

Affiliations

  • 1 Department of Gynecology, The Second Affiliated Hospital, School of Medicine and Life Sciences Institute, Zhejiang University, Hangzhou, China.
  • 2 MOE Laboratory of Biosystems Homeostasis and Protection and Innovation Center for Cell Signaling Network, Life Sciences Institute, Zhejiang University, Hangzhou, China.
  • 3 Cancer Center, Zhejiang University, Hangzhou, China.
  • 4 Center for Life Sciences, Shaoxing Institute, Zhejiang University, Shaoxing, China.
  • 5 Department of Oncology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
  • 6 School of Biomedical Sciences, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
  • 7 Department of Gynecology, The Second Affiliated Hospital, School of Medicine and Life Sciences Institute, Zhejiang University, Hangzhou, China. jianwei-zhou@zju.edu.cn.
  • 8 MOE Laboratory of Biosystems Homeostasis and Protection and Innovation Center for Cell Signaling Network, Life Sciences Institute, Zhejiang University, Hangzhou, China. dfang@zju.edu.cn.
  • 9 Department of Gynecology, The Second Affiliated Hospital, School of Medicine and Life Sciences Institute, Zhejiang University, Hangzhou, China. liuting518@zju.edu.cn.
  • 10 Department of Cell Biology, Zhejiang University School of Medicine, Hangzhou, China. liuting518@zju.edu.cn.
  • 11 Department of Gynecology, The Second Affiliated Hospital, School of Medicine and Life Sciences Institute, Zhejiang University, Hangzhou, China. jhuang@zju.edu.cn.
  • 12 MOE Laboratory of Biosystems Homeostasis and Protection and Innovation Center for Cell Signaling Network, Life Sciences Institute, Zhejiang University, Hangzhou, China. jhuang@zju.edu.cn.
  • 13 Cancer Center, Zhejiang University, Hangzhou, China. jhuang@zju.edu.cn.
  • 14 Center for Life Sciences, Shaoxing Institute, Zhejiang University, Shaoxing, China. jhuang@zju.edu.cn.
  • # Contributed equally.
Abstract

R-loops, comprising an RNA-DNA hybrid and a displaced single-stranded DNA, are dynamic three-stranded nucleic acid structures that, when dysregulated, can disrupt transcription and replication, undermining genome integrity and contributing to human pathologies. Here we identify exonuclease 3'-5' domain-containing 2 (EXD2) as a pivotal R-loop resolvase. We demonstrate that EXD2, through direct interaction with poly(ADP-ribose) (PAR) Polymers synthesized by R-loop-bound and activated PAR polymerase 1 (PARP1), is recruited to R-loops, where it undergoes acetylation by the acetyltransferase CREB-binding protein at K416. This modification increases EXD2's binding affinity toward R-loop structures, allowing stable association with these structures despite the rapid turnover of PAR Polymers. Once retained, EXD2 preferentially degrades RNA strands within R-loops to promote their resolution. Loss of EXD2 results in the intracellular accumulation of R-loops, exacerbating transcription-replication conflicts and ultimately leading to genomic instability. These findings support a model in which R-loop-triggered PARP1 activation orchestrates EXD2-mediated resolution of R-loops, thereby preserving genome stability.

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