ABSTRACT 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.
Compartmentalized DNA repair: Rif1 S-acylation links DNA double-strand break repair to the nuclear membrane
Gabriele A. Fontana,Ulrich Rass
Published 2019 in Molecular & Cellular Oncology
ABSTRACT
PUBLICATION RECORD
- Publication year
2019
- Venue
Molecular & Cellular Oncology
- Publication date
2019-08-21
- Fields of study
Biology, Medicine, Chemistry
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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