DNA Polymerase Delta Synthesizes Both Strands during Break-Induced Replication

被引:61
作者
Donnianni, Roberto A. [1 ]
Zhou, Zhi-Xiong [2 ]
Lujan, Scott A. [2 ]
Al-Zain, Amr [1 ]
Garcia, Valerie [1 ]
Glancy, Eleanor [1 ]
Burkholder, Adam B. [3 ]
Kunkel, Thomas A. [2 ]
Symington, Lorraine S. [1 ,4 ]
机构
[1] Columbia Univ, Irving Med Ctr, Dept Microbiol & Immunol, New York, NY 10032 USA
[2] NIEHS, Genome Integr & Struct Biol Lab, NIH, DHHS, POB 12233, Res Triangle Pk, NC 27709 USA
[3] NIEHS, Integrat Bioinformat Support Grp, NIH, DHHS, POB 12233, Res Triangle Pk, NC 27709 USA
[4] Columbia Univ, Dept Genet & Dev, Irving Med Ctr, New York, NY 10032 USA
关键词
HALF-CROSSOVERS; MPH1; HELICASE; IN-VIVO; RECOMBINATION; REPAIR; ALPHA; SUBUNIT; BUBBLE; LENGTH; RAD51;
D O I
10.1016/j.molcel.2019.07.033
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
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 delta) 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 delta replicates both the invading and the complementary strand during BIR. In support of this conclusion, we show that depletion of Pol delta from cells reduces BIR, whereas depletion of Pol epsilon has no effect.
引用
收藏
页码:371 / +
页数:15
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