DNA double-strand breaks (DSBs) disrupt the structural integrity of chromosomes. Proper DSB repair pathway choice is critical to avoid the type of gross chromosomal rearrangements that characterize cancer cells. Recent findings reveal S-fatty acylation and membrane anchorage of Rap1-interacting factor 1 (Rif1) as a mechanism providing spatial control over DSB repair pathway choice.
Keywords: DHHC palmitoyl transferases; HR; NHEJ; Pfa4; chromosome stability; protein palmitoylation.
© 2019 The Author(s). Published with license by Taylor & Francis Group, LLC.