共 34 条
Camptothecin-Induced Replication Stress Affects DNA Replication Profiling by E/L Repli-Seq
被引:5
作者:

Hayakawa, Takuya
论文数: 0 引用数: 0
h-index: 0
机构:
Mie Univ, Grad Sch Bioresources, Lab Mol & Cellular Biol, Tsu, Mie, Japan
Mie Univ, Tsuji Hlth & Beauty Sci Lab, Tsu, Mie, Japan
Tsuji Oil Mills Co Ltd, Matsusaka, Japan Mie Univ, Grad Sch Bioresources, Lab Mol & Cellular Biol, Tsu, Mie, Japan

Suzuki, Rino
论文数: 0 引用数: 0
h-index: 0
机构:
Mie Univ, Grad Sch Bioresources, Lab Mol & Cellular Biol, Tsu, Mie, Japan Mie Univ, Grad Sch Bioresources, Lab Mol & Cellular Biol, Tsu, Mie, Japan

Kagotani, Kazuhiro
论文数: 0 引用数: 0
h-index: 0
机构:
Mie Univ, Tsuji Hlth & Beauty Sci Lab, Tsu, Mie, Japan
Tsuji Oil Mills Co Ltd, Matsusaka, Japan Mie Univ, Grad Sch Bioresources, Lab Mol & Cellular Biol, Tsu, Mie, Japan

Okumura, Katsuzumi
论文数: 0 引用数: 0
h-index: 0
机构:
Mie Univ, Grad Sch Bioresources, Lab Mol & Cellular Biol, Tsu, Mie, Japan Mie Univ, Grad Sch Bioresources, Lab Mol & Cellular Biol, Tsu, Mie, Japan

Takebayashi, Shin-ichiro
论文数: 0 引用数: 0
h-index: 0
机构:
Mie Univ, Grad Sch Bioresources, Lab Mol & Cellular Biol, Tsu, Mie, Japan Mie Univ, Grad Sch Bioresources, Lab Mol & Cellular Biol, Tsu, Mie, Japan
机构:
[1] Mie Univ, Grad Sch Bioresources, Lab Mol & Cellular Biol, Tsu, Mie, Japan
[2] Mie Univ, Tsuji Hlth & Beauty Sci Lab, Tsu, Mie, Japan
[3] Tsuji Oil Mills Co Ltd, Matsusaka, Japan
基金:
日本科学技术振兴机构;
关键词:
DNA replication;
Replication stress;
E;
L Repli-seq;
Replication timing domain;
GENOME-WIDE;
ORIGINS;
DOMAINS;
CHK1;
RECOMBINATION;
ACTIVATION;
CELLS;
D O I:
10.1159/000518263
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
E/L Repli-seq is a powerful tool for detecting cell type-specific replication landscapes in mammalian cells, but its potential to monitor DNA replication under replication stress awaits better understanding. Here, we used E/L Repli-seq to examine the temporal order of DNA replication in human retinal pigment epithelium cells treated with the topoisomerase I inhibitor camptothecin. We found that the replication profiles by E/L Repli-seq exhibit characteristic patterns after replication-stress induction, including the loss of specific initiation zones within individual early replication timing domains. We also observed global disappearance of the replication timing domain structures in the profiles, which can be explained by checkpoint-dependent suppression of replication initiation. Thus, our results demonstrate the effectiveness of E/L Repli-seq at identifying cells with replication-stress-induced altered DNA replication programs.
引用
收藏
页码:437 / 444
页数:8
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