SETD2 loss-of-function promotes renal cancer branched evolution through replication stress and impaired DNA repair
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N Kanu Eva Gronroos P Martinez RA Burrell X Yi Goh J Bartkova A Maya-Mendoza M Mistrik Andrew Rowan H Patel A Rabinowitz Phil East Gareth Wilson CR Santos N McGranahan S Gulati M Gerlinger Nicolai Birkbak T Joshi LB Alexandrov MR Stratton T Powles N Matthews Paul Bates Aengus Stewart Z Szallasi J Larkin J Bartek Charles Swanton Toggle all authors (29)
Abstract
Defining mechanisms that generate intratumour heterogeneity and branched evolution may inspire novel therapeutic approaches to limit tumour diversity and adaptation. SETD2 (Su(var), Enhancer of zeste, Trithorax-domain containing 2) trimethylates histone-3 lysine-36 (H3K36me3) at sites of active transcription and is mutated in diverse tumour types, including clear cell renal carcinomas (ccRCCs). Distinct SETD2 mutations have been identified in spatially separated regions in ccRCC, indicative of intratumour heterogeneity. In this study, we have addressed the consequences of SETD2 loss-of-function through an integrated bioinformatics and functional genomics approach. We find that bi-allelic SETD2 aberrations are not associated with microsatellite instability in ccRCC. SETD2 depletion in ccRCC cells revealed aberrant and reduced nucleosome compaction and chromatin association of the key replication proteins minichromosome maintenance complex component (MCM7) and DNA polymerase δ hindering replication fork progression, and failure to load lens epithelium-derived growth factor and the Rad51 homologous recombination repair factor at DNA breaks. Consistent with these data, we observe chromosomal breakpoint locations are biased away from H3K36me3 sites in SETD2 wild-type ccRCCs relative to tumours with bi-allelic SETD2 aberrations and that H3K36me3-negative ccRCCs display elevated DNA damage in vivo. These data suggest a role for SETD2 in maintaining genome integrity through nucleosome stabilization, suppression of replication stress and the coordination of DNA repair.
Journal details
Journal Oncogene
Volume 34
Issue number 46
Pages 5699-5708
Available online
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Publisher website (DOI) 10.1038/onc.2015.24
Europe PubMed Central 25728682
Pubmed 25728682
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