Both High-Fidelity Replicative and Low-Fidelity Y-Family Polymerases Are Involved in DNA Rereplication

被引:11
|
作者
Sekimoto, Takayuki [1 ]
Oda, Tsukasa [1 ]
Kurashima, Kiminori [1 ]
Hanaoka, Fumio [2 ]
Yamashita, Takayuki [1 ]
机构
[1] Gunma Univ, Inst Mol & Cellular Regulat, Mol Genet Lab, Maebashi, Gunma 371, Japan
[2] Gakushuin Univ, Fac Sci, Tokyo 171, Japan
关键词
UBIQUITIN-BINDING DOMAINS; TRANSLESION SYNTHESIS; MONOUBIQUITINATED PCNA; MUTATIONAL PROCESSES; DAMAGE RESPONSE; STALLING SITES; POL-ETA; CHECKPOINT; CANCER; ROLES;
D O I
10.1128/MCB.01153-14
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA rereplication is a major form of aberrant replication that causes genomic instabilities, such as gene amplification. However, little is known about which DNA polymerases are involved in the process. Here, we report that low-fidelity Y-family polymerases (Y-Pols), Pol eta, Pol iota, Pol kappa, and REV1, significantly contribute to DNA synthesis during rereplication, while the replicative polymerases, Pol delta and Pol epsilon, play an important role in rereplication, as expected. When rereplication was induced by depletion of geminin, these polymerases were recruited to rereplication sites in human cell lines. This finding was supported by RNA interference (RNAi)-mediated knockdown of the polymerases, which suppressed rereplication induced by geminin depletion. Interestingly, epistatic analysis indicated that Y-Pols collaborate in a common pathway, independently of replicative polymerases. We also provide evidence for a catalytic role for Pol eta and the involvement of Pol eta and Pol kappa in cyclin E-induced rereplication. Collectively, our findings indicate that, unlike normal S-phase replication, rereplication induced by geminin depletion and oncogene activation requires significant contributions of both Y-Pols and replicative polymerases. These findings offer important mechanistic insights into cancer genomic instability.
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页码:699 / 715
页数:17
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