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Comprehensive Mutational Analysis of the BRCA1-Associated DNA Helicase and Tumor-Suppressor FANCJ/BACH1/BRIP1.
Calvo, Jennifer A; Fritchman, Briana; Hernandez, Desiree; Persky, Nicole S; Johannessen, Cory M; Piccioni, Federica; Kelch, Brian A; Cantor, Sharon B.
Affiliation
  • Calvo JA; Department of Molecular Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, Massachusetts.
  • Fritchman B; The Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
  • Hernandez D; The Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
  • Persky NS; The Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
  • Johannessen CM; The Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
  • Piccioni F; The Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
  • Kelch BA; Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, Massachusetts.
  • Cantor SB; Department of Molecular Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, Massachusetts. Sharon.Cantor@umassmed.edu.
Mol Cancer Res ; 19(6): 1015-1025, 2021 06.
Article in En | MEDLINE | ID: mdl-33619228
FANCJ (BRIP1/BACH1) is a hereditary breast and ovarian cancer (HBOC) gene encoding a DNA helicase. Similar to HBOC genes, BRCA1 and BRCA2, FANCJ is critical for processing DNA inter-strand crosslinks (ICL) induced by chemotherapeutics, such as cisplatin. Consequently, cells deficient in FANCJ or its catalytic activity are sensitive to ICL-inducing agents. Unfortunately, the majority of FANCJ clinical mutations remain uncharacterized, limiting therapeutic opportunities to effectively use cisplatin to treat tumors with mutated FANCJ. Here, we sought to perform a comprehensive screen to identify FANCJ loss-of-function (LOF) mutations. We developed a FANCJ lentivirus mutation library representing approximately 450 patient-derived FANCJ nonsense and missense mutations to introduce FANCJ mutants into FANCJ knockout (K/O) HeLa cells. We performed a high-throughput screen to identify FANCJ LOF mutants that, as compared with wild-type FANCJ, fail to robustly restore resistance to ICL-inducing agents, cisplatin or mitomycin C (MMC). On the basis of the failure to confer resistance to either cisplatin or MMC, we identified 26 missense and 25 nonsense LOF mutations. Nonsense mutations elucidated a relationship between location of truncation and ICL sensitivity, as the majority of nonsense mutations before amino acid 860 confer ICL sensitivity. Further validation of a subset of LOF mutations confirmed the ability of the screen to identify FANCJ mutations unable to confer ICL resistance. Finally, mapping the location of LOF mutations to a new homology model provides additional functional information. IMPLICATIONS: We identify 51 FANCJ LOF mutations, providing important classification of FANCJ mutations that will afford additional therapeutic strategies for affected patients.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA Mutational Analysis / DNA Helicases / BRCA1 Protein / RNA Helicases / Fanconi Anemia Complementation Group Proteins / Mutation / Neoplasms Type of study: Risk_factors_studies Limits: Humans Language: En Journal: Mol Cancer Res Journal subject: BIOLOGIA MOLECULAR / NEOPLASIAS Year: 2021 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA Mutational Analysis / DNA Helicases / BRCA1 Protein / RNA Helicases / Fanconi Anemia Complementation Group Proteins / Mutation / Neoplasms Type of study: Risk_factors_studies Limits: Humans Language: En Journal: Mol Cancer Res Journal subject: BIOLOGIA MOLECULAR / NEOPLASIAS Year: 2021 Type: Article