PARPi synthetic lethality derives from replication-associated single-stranded DNA gaps

Author:

Cong Ke,Kousholt Arne Nedergaard,Peng Min,Panzarino Nicholas J.,Lee Wei Ting Chelsea,Nayak Sumeet,Krais John,Calvo Jennifer,Bere Matt,Rothenberg Eli,Johnson Neil,Jonkers Jos,Cantor Sharon B.

Abstract

AbstractBRCA1 or BRCA2 (BRCA)-deficient tumor cells have defects in DNA double strand break repair by homologous recombination (HR) and fork protection (FP) that are thought to underlie the sensitivity to poly(ADP-ribose) polymerase inhibitor (PARPi). Given the recent finding that PARPi accelerates DNA replication, it was proposed that high speed DNA replication leads to DNA double strand breaks (DSBs). Here, we tested the alternative hypothesis that PARPi sensitivity in BRCA deficient cells results from combined replication dysfunction that causes a lethal accumulation of replication-associated single-stranded DNA (ssDNA) gaps. In support of a gap toxicity threshold, PARPi-induced ssDNA gaps accumulate more excessively in BRCA deficient cells and are suppressed in de novo and genetic models of PARPi resistance while defects in HR or FP often lack this correlation. We also uncouple replication speed from lethality. The clear link between PARPi sensitivity and ssDNA gaps provides a new paradigm for understanding synthetic lethal interactions.

Publisher

Cold Spring Harbor Laboratory

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