Genome-wide Determination of Mammalian Replication Timing by DNA Content Measurement

被引:4
作者
Yehuda, Yishai [1 ]
Blumenfeld, Britny [1 ]
Lehmann, Dan [2 ]
Simon, Itamar [1 ]
机构
[1] Hebrew Univ Jerusalem, Fac Med, IMRIC, Dept Microbiol & Mol Genet, Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Fac Med, IMRIC, Core Res Facil, Jerusalem, Israel
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2017年 / 119期
基金
欧洲研究理事会; 以色列科学基金会;
关键词
Genetics; Issue; 119; Genomics; Replication; FACS; Sequencing; Bioinformatics; Replication Timing; TIME ZONES; DOMAINS; MUTATION;
D O I
10.3791/55157
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Replication of the genome occurs during S phase of the cell cycle in a highly regulated process that ensures the fidelity of DNA duplication. Each genomic region is replicated at a distinct time during S phase through the simultaneous activation of multiple origins of replication. Time of replication (ToR) correlates with many genomic and epigenetic features and is linked to mutation rates and cancer. Comprehending the full genomic view of the replication program, in health and disease is a major future goal and challenge. This article describes in detail the "Copy Number Ratio of S/G1 for mapping genomic Time of Replication" method (herein called: CNR-ToR), a simple approach to map the genome wide ToR of mammalian cells. The method is based on the copy number differences between S phase cells and G1 phase cells. The CNR-ToR method is performed in 6 steps: 1. Preparation of cells and staining with propidium iodide (PI); 2. Sorting G1 and S phase cells using fluorescence-activated cell sorting (FACS); 3. DNA purification; 4. Sonication; 5. Library preparation and sequencing; and 6. Bioinformatic analysis. The CNR-ToR method is a fast and easy approach that results in detailed replication maps.
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页数:8
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