bioRxiv · 10.1101/176271
The helicase domain of Polθ counteracts RPA to promote alt-NHEJ
Abstract
Mammalian polymerase theta (Pol{theta}; encoded by POLQ) is a unique multifunctional enzyme that promotes error-prone DNA repair by alternative-NHEJ (alt-NHEJ). Here we perform structure-function analyses and report that, in addition to the polymerase domain, the helicase activity plays a central role during Pol{theta}-mediated double-stranded break (DSB) repair. Our results show that Pol{theta}-helicase promotes chromosomal translocations by alt-NHEJ in mouse embryonic stem cells. In addition, the helicase activity suppresses CRISPR/Cas9 mediated gene targeting by homologous recombination (HR). In vitro experiments reveal that Pol{theta}-helicase displaces RPA to facilitate the annealing of complementary DNA during alt-NHEJ. Consistent with an antagonistic role for RPA during alt-NHEJ, we show that the inhibition of RPA1 subunit enhances end-joining and suppresses recombination at telomeres. Taken together, our results reveal that the balance between HR and alt-NHEJ is regulated by opposing activities of Pol{theta} and RPA, providing critical insight into the mechanism that control DSB repair pathway choice in mammalian cells.
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Mateos-Gomez, P. A., Kashkina, E., Pomerantz, R., Kent, T., Sfeir, A.. 2017-08-14. The helicase domain of Polθ counteracts RPA to promote alt-NHEJ. https://doi.org/10.1101/176271
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