| Literature DB >> 31495565 |
Roberto A Donnianni1, Zhi-Xiong Zhou2, Scott A Lujan2, Amr Al-Zain1, Valerie Garcia1, Eleanor Glancy1, Adam B Burkholder3, Thomas A Kunkel2, Lorraine S Symington4.
Abstract
Break-induced replication (BIR) is a pathway of homology-directed repair that repairs one-ended DNA breaks, such as those formed at broken replication forks or uncapped telomeres. In contrast to conventional S phase DNA synthesis, BIR proceeds by a migrating D-loop and results in conservative synthesis of the nascent strands. DNA polymerase delta (Pol δ) initiates BIR; however, it is not known whether synthesis of the invading strand switches to a different polymerase or how the complementary strand is synthesized. By using alleles of the replicative DNA polymerases that are permissive for ribonucleotide incorporation, thus generating a signature of their action in the genome that can be identified by hydrolytic end sequencing, we show that Pol δ replicates both the invading and the complementary strand during BIR. In support of this conclusion, we show that depletion of Pol δ from cells reduces BIR, whereas depletion of Pol ε has no effect.Entities:
Keywords: DNA polymerase delta; DNA repair; break-induced replication; homologous recombination
Mesh:
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Year: 2019 PMID: 31495565 PMCID: PMC6862718 DOI: 10.1016/j.molcel.2019.07.033
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970