RT Journal Article
SR Electronic
T1 Global Epigenetic Analysis Reveals H3K27 Methylation as a Mediator of Double Strand Break Repair
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 2021.09.20.461136
DO 10.1101/2021.09.20.461136
A1 Julian Lutze
A1 Donald Wolfgeher
A1 Stephen J. Kron
YR 2021
UL http://biorxiv.org/content/early/2021/09/20/2021.09.20.461136.abstract
AB The majority of cancer patients is treated with ionizing radiation (IR), a relatively safe and effective treatment considered to target tumors by inducing DNA double strand breaks (DSBs). Despite clinical interest in increasing the efficacy of IR by preventing successful DSB repair, few effective radio-adjuvant therapies exist. Extensive literature suggests that chromatin modifiers play a role in the DSB repair and thus may represent a novel class of radiosensitizers. Indeed, chromatin has both local and global impacts on DSB formation, recognition of breaks, checkpoint signaling, recruitment of repair factors, and timely DSB resolution, suggesting that epigenetic deregulation in cancer may impact the efficacy of radiotherapy. Here, using tandem mass spectrometry proteomics to analyze global patterns of histone modification in MCF7 breast cancer cells following IR exposure, we find significant and long-lasting changes to the epigenome. Our results confirm that H3K27 trimethylation (H3K27me3), best known for mediating gene repression and regulating cell fate, increases after IR. H3K27me3 changes rapidly, accumulating at sites of DNA damage. Inhibitors of the Polycomb related complex subunit and H3K27 methyltransferase EZH2 confirm that H3K27me3 is necessary for DNA damage recognition and cell survival after IR. These studies provide an argument for evaluating EZH2 as a radiosensitization target and H3K27me3 as a marker for radiation response in cancer. Proteomic data are available via ProteomeXchange with identifier PXD019388.Competing Interest StatementThe authors have declared no competing interest.AMTAccurate Mass and timeATMAtaxia telangiectasia mutatedATRAtaxia telangiectasia and Rad3 relatedDDRDNA Damage ResponseDSBDouble Strand BreakDNA-PKcsDNA-dependent Protein KinaseEHMPEpiproteomic Histone Modification PanelEZH2Enhancer of Zest Homologue 2FRETFörster Resonance Energy TransferγH2AXgamma H2AX is the phosphorylated form of H2AXHRHomologous RecombinationIRIonizing RadiationIRIFIonizing Radiation Induced FociNHEJNon-homologous End JoiningMRMMultiple Reaction MonitoringPARPPoly ADP-ribose PolymerasePIKKPhosphatidylinositol 3-kinase-related kinasesPIRPost-IRPol IIRNA Polymerase IIPRC2Polycomb Repressive Complex 2PTMPost Translational Modification