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CRISPR screens identify genomic ribonucleotides as a source of PARP-trapping lesions.

Zimmermann, Michal and Murina, Olga and Reijns, Martin A M and Agathanggelou, Angelo and Challis, Rachel and Tarnauskaitė, Žygimantė and Muir, Morwenna and Fluteau, Adeline and Aregger, Michael and McEwan, Andrea and Yuan, Wei and Clarke, Matthew and Lambros, Maryou B and Paneesha, Shankara and Moss, Paul and Chandrashekhar, Megha and Angers, Stephane and Moffat, Jason and Brunton, Valerie G and Hart, Traver and de Bono, Johann and Stankovic, Tatjana and Jackson, Andrew P and Durocher, Daniel (2018) CRISPR screens identify genomic ribonucleotides as a source of PARP-trapping lesions. Nature. ISSN 1476-4687.

Full text not available from this repository.
Official URL: http://www.nature.com/articles/s41586-018-0291-z

Abstract

The observation that BRCA1- and BRCA2-deficient cells are sensitive to inhibitors of poly(ADP-ribose) polymerase (PARP) has spurred the development of cancer therapies that use these inhibitors to target deficiencies in homologous recombination. The cytotoxicity of PARP inhibitors depends on PARP trapping, the formation of non-covalent protein-DNA adducts composed of inhibited PARP1 bound to DNA lesions of unclear origins. To address the nature of such lesions and the cellular consequences of PARP trapping, we undertook three CRISPR (clustered regularly interspersed palindromic repeats) screens to identify genes and pathways that mediate cellular resistance to olaparib, a clinically approved PARP inhibitor. Here we present a high-confidence set of 73 genes, which when mutated cause increased sensitivity to PARP inhibitors. In addition to an expected enrichment for genes related to homologous recombination, we discovered that mutations in all three genes encoding ribonuclease H2 sensitized cells to PARP inhibition. We establish that the underlying cause of the PARP-inhibitor hypersensitivity of cells deficient in ribonuclease H2 is impaired ribonucleotide excision repair. Embedded ribonucleotides, which are abundant in the genome of cells deficient in ribonucleotide excision repair, are substrates for cleavage by topoisomerase 1, resulting in PARP-trapping lesions that impede DNA replication and endanger genome integrity. We conclude that genomic ribonucleotides are a hitherto unappreciated source of PARP-trapping DNA lesions, and that the frequent deletion of RNASEH2B in metastatic prostate cancer and chronic lymphocytic leukaemia could provide an opportunity to exploit these findings therapeutically.

Item Type: Article
Subjects: QZ Pathology. Oncology
Divisions: Planned IP Care > Oncology and Clinical Haematology
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Depositing User: Mrs Yolande Brookes
Date Deposited: 06 Jul 2018 13:05
Last Modified: 06 Jul 2018 13:05
URI: http://www.repository.heartofengland.nhs.uk/id/eprint/1687

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