DescriptionHomologous recombinational repair of DNA double-strand damage.jpg
English: Recombinational repair of DNA double-strand damage - some key steps.ATM (ATM) is a protein kinase that is recruited and activated by DNA double-strand breaks. DNA double-strand damages also activate the Fanconi anemia core complex (FANCA/B/C/E/F/G/L/M).[1] The FA core complex monoubiquitinates the downstream targets FANCD2 and FANCI.[2] ATM activates (phosphorylates) CHEK2 and FANCD2.[3] CHEK2 phosphorylates BRCA1.[4] Ubiquinated FANCD2 complexes with BRCA1 and RAD51.[5] The PALB2 protein acts as a hub,[6] bringing together BRCA1, BRCA2 and RAD51 at the site of a DNA double-strand break, and also binds to RAD51C, a member of the RAD51 paralog complex RAD51B-RAD51C-RAD51D-XRCC2 (BCDX2). The BCDX2 complex is responsible for RAD51 recruitment or stabilization at damage sites.[7]RAD51 plays a major role in homologous recombinational repair of DNA during double strand break repair. In this process, an ATP dependent DNA strand exchange takes place in which a single strand invades base-paired strands of homologous DNA molecules. RAD51 is involved in the search for homology and strand pairing stages of the process.
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↑ (2011). "Coordinated action of the Fanconi anemia and ataxia telangiectasia pathways in response to oxidative damage". DNA Repair (Amst.)10 (5): 518–25. DOI:10.1016/j.dnarep.2011.02.007. PMID21466974.
↑ (2011). "Tumor suppressor CHK2: regulator of DNA damage response and mediator of chromosomal stability". Clin. Cancer Res.17 (3): 401–5. DOI:10.1158/1078-0432.CCR-10-1215. PMID21088254.
↑ (2002). "S-phase-specific interaction of the Fanconi anemia protein, FANCD2, with BRCA1 and RAD51". Blood100 (7): 2414–20. DOI:10.1182/blood-2002-01-0278. PMID12239151.