{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Sarkar D"],"funding":["Department of Atomic Energy, Government of India","Science and Engineering Research Board","Indian Council of Medical Research","Department of Biotechnology, Ministry of Science and Technology, India"],"pagination":["446"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11544116"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["81(1)"],"pubmed_abstract":["Efficient DNA double strand break (DSB) repair is necessary for genomic stability and determines efficacy of DNA damaging cancer therapeutics. Spatiotemporal dynamics and post-translational modifications of repair proteins at DSBs dictate repair efficacy. Here, we identified a non-canonical function of GCN5 in regulating both HR and NHEJ repair post genotoxic stress. Mechanistically, genotoxic stress induced GCN5 recruitment to DSBs. GCN5 PARylation by PARP1 was essential for its recruitment, acetyltransferase activity and DSB repair function. Liquid chromatography-mass spectrometry (LC-MS) identified DNA-PKcs as part of GCN5 interactome. In-vitro acetyltransferase assays revealed that GCN5 acetylates DNA-PKcs at K3241 residue, a prerequisite for DNA-PKcs S2056 phosphorylation and DSB recr"],"journal":["Cellular and molecular life sciences : CMLS"],"pubmed_title":["PARylation of GCN5 by PARP1 mediates its recruitment to DSBs and facilitates both HR and NHEJ Repair."],"pmcid":["PMC11544116"],"funding_grant_id":["BMS/TF/TRANS-NEURO/2014-3646/Dec-2015/48/MH/GOVT","EMR/2017/004994","BT/PR13863/MED/122/6/2016","1/3(6)/2020/TMC/R&D-II/3805","1/3(7)/2020/TMC/R&D-II/8823"],"pubmed_authors":["Mandi S","Sarkar D","Dutt S","Chakraborty A"],"additional_accession":[]},"is_claimable":false,"name":"PARylation of GCN5 by PARP1 mediates its recruitment to DSBs and facilitates both HR and NHEJ Repair.","description":"Efficient DNA double strand break (DSB) repair is necessary for genomic stability and determines efficacy of DNA damaging cancer therapeutics. Spatiotemporal dynamics and post-translational modifications of repair proteins at DSBs dictate repair efficacy. Here, we identified a non-canonical function of GCN5 in regulating both HR and NHEJ repair post genotoxic stress. Mechanistically, genotoxic stress induced GCN5 recruitment to DSBs. GCN5 PARylation by PARP1 was essential for its recruitment, acetyltransferase activity and DSB repair function. Liquid chromatography-mass spectrometry (LC-MS) identified DNA-PKcs as part of GCN5 interactome. In-vitro acetyltransferase assays revealed that GCN5 acetylates DNA-PKcs at K3241 residue, a prerequisite for DNA-PKcs S2056 phosphorylation and DSB recr","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Nov","modification":"2025-04-22T16:26:23.242Z","creation":"2025-04-06T01:45:49.136Z"},"accession":"S-EPMC11544116","cross_references":{"pubmed":["39508866"],"doi":["10.1007/s00018-024-05469-9"]}}