WIP1 Contributes to the Adaptation of Fanconi Anemia Cells to DNA Damage as Determined by the Regulatory Network of the Fanconi Anemia and Checkpoint Recovery Pathways

• Published in: Frontiers in genetics 2019-05, Vol.10, p.411-411
• Main Authors: Rodríguez, Alfredo, Naveja, J Jesús, Torres, Leda, García de Teresa, Benilde, Juárez-Figueroa, Ulises, Ayala-Zambrano, Cecilia, Azpeitia, Eugenio, Mendoza, Luis, Frías, Sara
• Format: Article
• Language: English
• Subjects: CHKREC; DNA damage adaptation; FA/BRCA pathway; Fanconi anemia; Genetics; ICLs; WIP1
• ISSN: 1664-8021; 1664-8021
• DOI: 10.3389/fgene.2019.00411

DNA damage adaptation (DDA) allows the division of cells with unrepaired DNA damage. DNA repair deficient cells might take advantage of DDA to survive. The Fanconi anemia (FA) pathway repairs DNA interstrand crosslinks (ICLs), and deficiencies in this pathway cause a fraction of breast and ovarian cancers as well as FA, a chromosome instability syndrome characterized by bone marrow failure and cancer predisposition. FA cells are hypersensitive to ICLs; however, DDA might promote their survival. We present the FA-CHKREC Boolean Network Model, which explores how FA cells might use DDA. The model integrates the FA pathway with the G2 checkpoint and the checkpoint recovery (CHKREC) processes. The G2 checkpoint mediates cell-cycle arrest (CCA) and the CHKREC activates cell-cycle progression (CCP) after resolution of DNA damage. Analysis of the FA-CHKREC network indicates that CHKREC drives DDA in FA cells, ignoring the presence of unrepaired DNA damage and allowing their division. Experimental inhibition of WIP1, a CHKREC component, in FA lymphoblast and cancer cell lines prevented division of FA cells, in agreement with the prediction of the model.