| Literature DB >> 29141206 |
Olga Buzovetsky1, Youngho Kwon1, Nhung Tuyet Pham2, Claire Kim1, Grzegorz Ira3, Patrick Sung4, Yong Xiong5.
Abstract
The S. cerevisiae Pif1 helicase functions with DNA polymerase (Pol) δ in DNA synthesis during break-induced replication (BIR), a conserved pathway responsible for replication fork repair and telomere recombination. Pif1 interacts with the DNA polymerase processivity clamp PCNA, but the functional significance of the Pif1-PCNA complex remains to be elucidated. Here, we solve the crystal structure of PCNA in complex with a non-canonical PCNA-interacting motif in Pif1. The structure guides the construction of a Pif1 mutant that is deficient in PCNA interaction. This mutation impairs the ability of Pif1 to enhance DNA strand displacement synthesis by Pol δ in vitro and also the efficiency of BIR in cells. These results provide insights into the role of the Pif1-PCNA-Pol δ ensemble during DNA break repair by homologous recombination.Entities:
Keywords: DNA polymerase δ; PCNA; PIP box; Pif1; break induced replication; homologous recombination
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Year: 2017 PMID: 29141206 PMCID: PMC5842794 DOI: 10.1016/j.celrep.2017.10.079
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423